UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

FORM 10-K
ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d)
OF THE SECURITIES EXCHANGE ACT OF 1934

For The Fiscal Year Ended December 31, 20062007

Commission File Number 333-31932001-31932

Hythiam, Inc.
(Exact name of registrant as specified in its charter)


   
Delaware 88-0464853
(State or other jurisdiction of incorporation) (I.R.S. Employer Identification Number)

11150 Santa Monica Boulevard, Suite 1500
Los Angeles, California 90025
(Address of principal executive offices, including zip code)

(310) 444-4300
(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

Common Stock, $0.0001 par value Nasdaq Global Market
(Title of each class) (Name of each exchange on which registered)


Securities registered pursuant to Section 12(g) of the ActNone

Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act.

Yeso     Noþ

Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act.

Yeso     Noþ

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Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.

Yesþ Noo

Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K is not contained herein, and will not be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of the Form 10-K or any amendment to this Form 10-K.þ

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, or a non-accelerated filer. See definition of ‘‘accelerated filer and large accelerated filer’’ in Rule 12b-2 of the Exchange Act. (Check one):

Large accelerated filero       Accelerated filerþ       Non-accelerated filero
 Accelerated filer   þ
 Non-accelerated filer    o
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).
Yeso     Noþ
As of June 30, 2006,2007, the aggregate market value of the common stock held by non-affiliates of the registrant was $179,096,520,$264,125,000 based on the $6.97$8.65 closing price on the Nasdaq Global Market on that date. This amount excludes the value of 13,966,666$120,812,000 shares of common stock directly or indirectly held by the registrant’s affiliates.

As of March 13, 2007,14, 2008, there were 44,295,099 54,387,604 shares of the registrant’s common stock outstanding.

DOCUMENTS INCORPORATED BY REFERENCE

Portions of the registrant’s proxy statement for its 20072008 annual meeting of stockholders to be held on June 15, 2007,20, 2008, are incorporated by reference into Part III of this report.
 


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HYTHIAM, INC.
Form 10-K Annual Report
For The Fiscal Year Ended December 31, 20062007

TABLE
TABLE OF CONTENTS
   
 
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Exhibit 10.810.13
Exhibit 10.9
Exhibit 10.10
Exhibit 10.1110.15
Exhibit 21.1
Exhibit 23.1
Exhibit 23.2
Exhibit 31.1
Exhibit 31.2
Exhibit 32.1
Exhibit 32.2
EXHIBIT 10.8
EXHIBIT 10.9
EXHIBIT 10.10
EXHIBIT 10.11
EXHIBIT 21.1
EXHIBIT 23.1
EXHIBIT 31.1
EXHIBIT 31.2
EXHIBIT 32.1
EXHIBIT 32.2

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PART I
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Forward-Looking Statements

This report contains forward-looking statements that involve risks and uncertainties. Our actual results may differ materially from those discussed due to factors such as, among others, limited operating history, difficulty in developing, exploiting and protecting proprietary technologies, intense competition and substantial regulation in the healthcare industry. Additional information concerning factors that could cause or contribute to such differences can be found in the following discussion, as well as in Item 1.A Risk Factors and Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

ITEM 1.                  BUSINESS
Overview
Overview

We are a healthcare services management company, focused on delivering solutions for those suffering from alcoholismintegrating both medical and other substance dependencies.psychosocial treatment modalities, providing behavioral health management services to health plans, employers, criminal justice and government agencies through a network of licensed and company-managed healthcare providers. We also research, develop, license and commercialize innovative physiological, nutritional and behavioral treatment protocols.programs. We manage behavioral health disorders through our subsidiary, Comprehensive Care Corporation (CompCare), in which we acquired a majority controlling interest in January 2007. We approach the management of behavioral health disorders with a focus on using the latest medical and health technology towards improved outcomes and outpatient treatment.  We offer disease management programs for substance dependence built around our proprietarypatented PROMETA® treatment protocols Treatment Programs for alcoholism and dependence to stimulants.cocaine and methamphetamines. Our proprietary PROMETA Treatment with our PROMETA protocols, whichPrograms--which integrate behavioral, nutritional and medical components, arecomponents--are available only through physicians and other licensed treatment providers who have entered into licensing agreements with us for the use of our protocols.treatment programs. We also manage or license PROMETA Centers, medical practices and treatment centers that focus on offering treatment withoffer the PROMETA protocolsTreatment Programs, as well as other treatments for dependencies on alcohol, cocaine and methamphetamines.substance dependencies. 

Our PROMETA basedPROMETA-based disease management programs allow healthcare providers who license our technology to offer an integrated approach for the treatment of substance dependence that can be tailored for the specific needs of patients with medical and psychiatric comorbidities.
     We have invested significant resources for business development, sales, marketing, research, development and other activities in order to implement commercial operations and establish market penetration. Our revenues are growing and we anticipate they will continue to grow significantly due to:
increases in the level of private pay patients from existing licensees and PROMETA Centers
greater numbers of managed care and government providers adopting our protocols based on successful results from commercial pilots and scientific studies
expansion into new markets such as managed care.
     We have been unprofitable since our inception in 2003 and expect to continue to incur operating losses for some time. However, we believe our operating losses will decrease and we will achieve positive cash flows within the next two years as the number of patients treated with PROMETA continues to increase. Accordingly, our historical operations and financial information are not necessarily indicative of future operating results, financial condition or ability to operate profitably as a commercial enterprise.
CompCare Acquisition
     On January 12, 2007, we acquired a majority controlling interest in Comprehensive Care Corporation (CompCare) through the acquisition of Woodcliff Healthcare Investment Partners, LLP. Effective as of our acquisition of Woodcliff, our consolidated financial statements will include the business and operations of CompCare as our majority-owned, controlled subsidiary.
     CompCare, primarily through its wholly-owned subsidiary, Comprehensive Behavioral Care, Inc., provides managed care services in the behavioral health and psychiatric fields. CompCare manages the delivery of a

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continuum of psychiatric and substance abuse services to commercial, Medicare and Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators and commercial and other group purchasers of behavioral healthcare services. The customer base for CompCare’s services includes both private and governmental entities.
     Since February 2006, we have had a marketing agreement with CompCare under which CompCare has the right to offer our protocols as part of a disease management offering to its customers and other mutually agreed parties on an exclusive basis. We believe our relationship with CompCare will create synergies and efficiencies allowing us to more effectively and efficiently facilitate adoption and use of our protocols among treatment populations managed or reimbursed by third party payers, such as managed care, primarily through a disease management offering. CompCare provides an infrastructure to offer this PROMETA-based disease management, to enable healthcare providers to offer an integrated approach for the treatment of substance dependence.
     On January 18, 2007, we entered into a merger agreement with CompCare, amended January 26, 2007, pursuant to which we would acquire the remaining outstanding shares of CompCare in exchange for shares of our common stock. However, two stockholder class actions were filed in the Delaware Court of Chancery seeking to enjoin the proposed merger. If the litigation is resolved quickly on reasonable terms, the merger should be consummated in the second quarter. If we determine we are unlikely to settle the litigation on acceptable terms within a reasonable period of time, the parties will likely terminate the merger agreement by mutual written consent. In that event, CompCare will continue as our majority-owned, controlled subsidiary for the foreseeable future. We believe we can effectuate substantially all of the benefits of our relationship with CompCare under our current operational structure.
PROMETA®
Our unique PROMETA protocols are unique treatment protocolsTreatment Programs for alcohol, cocaine orand methamphetamine dependence that integrate physiological, nutritional and psychosocial therapies designed to help patients meet their individual recovery goals. PROMETA protocols are specifically designedTreatment Programs seek to target key neuroreceptors to help relieve cravings and improve cognitive function, restore nutritional balance and initiate psychosocial counseling, so that patients can fully engage in the entire recovery process. Our two proprietary PROMETA treatment protocols,Treatment Programs, one for alcohol dependence and the other for stimulant dependence or a combination of alcohol and stimulant dependence, incorporate FDA-approved oral and IV medications usedprescribed off-label and separately administered in a unique dosing algorithm. The pharmacologic intervention is integrated with nutritional support and the selection and initiation of psychosocial therapy. As a result, our PROMETA protocolsTreatment Programs represent an innovative approach to substance dependence designed to address physiological, nutritional and psychosocial aspects of the disease, and are thereby intended to offer patients an opportunity to achieve sustained recovery.

Historically, the disease of addiction has been treated primarily through behavioral intervention, with fairly high relapse rates. We believe the PROMETA Treatment Programs offer an advantage to traditional alternatives because they provide a treatment methodology that is discreet and only mildly sedating and can be initiated in only three days, with a two-day follow-up treatment three weeks later for addictive stimulants. Our PROMETA


Treatment Programs also provide for one month of prescription medication and nutritional supplements, combined with psychosocial or other recovery-oriented therapy chosen by the patient in conjunction with their treatment provider. The medical treatment is followed by continuing care, such as individual or group counseling, as a key part of recovery. Limited initial clinical observations indicate that our treatment programs may improve cognitive function, reduce withdrawal symptoms, be associated with higher initial completion rates than conventional treatments, and reduce physical cravings which can be a major factor in relapse, thus allowing patients to more meaningfully engage in counseling or other forms of psychosocial therapy.

We believe the short initial treatment period when using our PROMETA Treatment Programs is a major advantage over traditional inpatient detoxification treatments and residential treatment programs, which typically consist of up to 28 days of combined inpatient detoxification and recovery in a rehabilitation or residential treatment center. Treatment with PROMETA does not require an extensive stay at an inpatient facility. Rather, the PROMETA Treatment Programs offer the convenience of a three-day treatment (for addictive stimulants there is a two-day follow-up treatment three weeks later) and can be administered on an outpatient basis. This is particularly relevant since results from the National Survey on Drug Use and Health – 2006 reported that approximately 75% of adults  using illicit drugs in 2006 were employed, and loss of time from work can be a significant deterrent from seeking treatment.

We have been unprofitable since our inception in 2003 and expect to continue to incur operating losses for at least the next twelve months.  However, we believe our operating losses will decrease and we will achieve positive cash flows within the next two years as the number of patients treated with the PROMETA Treatment Program increases.  Accordingly, our historical operations and financial information are not necessarily indicative of future operating results, financial condition or ability to operate profitably as a commercial enterprise.

We believe that our business and operations as outlined above are in substantial compliance with applicable laws and regulations. However, the healthcare industry is highly regulated, and the criteria are often vague and subject to change and interpretation by various federal and state legislatures, courts, enforcement and regulatory authorities. ClinicalAdditional clinical studies are underway to evaluate our protocolstreatment programs and confirm initial studies and reports from physicians using them in their practices. Only a treating physician can determine if PROMETA is appropriate for any individual patient. The medications used in the PROMETA treatment protocolsTreatment Programs are FDA approved for uses other than treating dependence on alcohol, cocaine or methamphetamine. Therefore, the risks and benefits of using those medications to treat dependence on those substances have not been evaluated by the FDA, which may not find them to be sufficiently safe or effective. We do not manufacture, distribute or sell any medications and have no relationship with any manufacturers or distributors of medications used in the PROMETA protocols.Treatment Programs. Only a treating physician can determine if the PROMETA Treatment Program is appropriate for any individual patient. Our future prospects are subject to the legal, regulatory, commercial and scientific risks outlined above and in Item 1.A Risk Factors.
Our Strategy
     Our business strategy is to provide quality treatment protocols that will become the standard-of-careMarket for those suffering from alcoholism and other substance dependencies at a lower overall cost than traditional treatment approaches. We intend to grow our business through increased utilization from within existing and new licensees, additional PROMETA Centers, and increased adoption of our PROMETA protocols and substance abuse disease management treatment approach by government agencies, criminal justice systems, managed care and other third-party payers.

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Key elements of our business strategy include:®
Expanding the base of our licensed treatment sites, focusing on existing service areas
Increasing the number of dedicated PROMETA Centers in major U.S. markets
Demonstrating the potential for improved clinical outcomes and cost effectiveness associated with using the PROMETA treatment protocols, through commercial pilot studies with key managed care and other third-party payers
Leveraging existing and initiating new pilot studies with governmental agencies to accelerate the adoption and funding by criminal justice, state and local government systems
Providing our substance abuse disease management program to managed care health plans for reimbursement on a case rate or capitated basis, utilizing the CompCare infrastructure to provide basic managed care services
Seeking additional scientific and clinical research data to further validate the efficacy of using the PROMETA protocols through unrestricted grants for research studies by leading research institutions and preeminent researchers in the field of alcohol and substance abuse
Exploring opportunities in foreign markets where our PROMETA patents have issued

Expand Number of Licensees in U.S.
     We will focus on expanding our presence in the U.S. private payer market by targeting existing service areas, and licensing our protocols and providing our services to additional healthcare providers in those areas. Furthermore, we will provide our licensees with a comprehensive level of added-value services to enhance their ability to communicate the scientific rationale and clinical relevancy of the PROMETA protocols. Our primary focus will be in major metropolitan service areas where we have already established a market presence in order to leverage our site managers, marketing efforts and brand awareness of PROMETA and benefit from resulting treatment volumes on a cost-effective basis without capacity constraint.
     In February 2007 we launched a new nationwide team of field personnel focused on increasing awareness and utilization of the PROMETA protocols among physicians and allied health professionals specializing in the treatment of substance dependence. Our national field organization comprises a total of 36 individuals, 18 PROMETA clinical consultants (PCCs) and 18 site managers. Site managers will service our nationwide footprint of over 60 PROMETA licensed sites in 18 markets, having primary responsibility to enable our licensees to increase utilization from within their practice. PCCs will also serve the existing licensed sites by communicating the scientific rationale and clinical relevancy of the treatment protocols to a broader targeted audience in order to enhance our existing licensees’ ability to increase their prospective PROMETA patient flow. Additionally, we now have six dedicated business development directors to work closely with our site managers and PCCs in an effort to quickly identify new potential licensees and execute broad strategies for increasing the visibility of the licensed sites within their respective regions.
     As additional data from research studies become available, we plan to expand our marketing initiatives to more aggressively educate the professional community (e.g., physicians, counselors, therapists, payers and other allied professionals). This staged strategic approach to our marketing efforts takes into account:
(i)the potential benefits of increasing physician and patient awareness of PROMETA
(ii)that a more robust data dossier will facilitate broader adoption of PROMETA by patients and the treatment community.

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PROMETA Centers
     In December 2005, David E. Smith, M.D., a renowned addiction medicine specialist and founder of the Haight Ashbury Free Clinics, opened the first PROMETA Center®, a new medical practice operating in a state-of-the-art outpatient facility in Santa Monica, California, and in January 2007, opened a second PROMETA Center in San Francisco, both of which are located in medical office space that we leased and built out. Under the terms of a full business service management agreement with Dr. Smith’s professional corporation, The PROMETA Center, Inc., we manage the business components of the practice and license the PROMETA protocols and use of the name in exchange for management and licensing fees. The medical practice has a focus on offering treatment with the PROMETA protocols for dependencies on alcohol, cocaine and methamphetamines, and also offers medical interventions for other substance dependencies. Under generally accepted accounting principals, the revenues and expenses of The PROMETA Center, Inc. are included in our consolidated financial statements.
     In January 2007, a new PROMETA Center medical practice was opened in New Jersey, managed by the Canterbury Institute. Under the terms of our licensing agreement with Canterbury, we will receive fees for services and technology licensing and a 10% share of the profits made by Canterbury from its owned or managed PROMETA Centers. Canterbury plans to manage an additional PROMETA Center to be opened in Boca Raton, Florida in the second quarter of 2007.
     Based on the success of this business model, our strategy is to license or manage additional PROMETA Centers in major markets in the U.S., including markets currently served only by PROMETA licensees over the next two years.
Managed Care
     We plan to continue positioning PROMETA with managed care providers and disease-state management programs with the goal of becoming a covered benefit under managed care programs. Pilots with major health plans now underway to conduct commercial evaluations of our PROMETA protocols as a central component for substance dependence disease management are expected to be completed this year.
     We believe our association with CompCare creates synergies to facilitate the use of our PROMETA treatment protocols by managed care treatment providers and provide access to an infrastructure for our substance abuse disease management offerings. Key strategies and benefits expected from our association with CompCare include the following:
A network of 8,000 CompCare providers that can increase the potential referral base and availability of PROMETA at treatment sites. CompCare currently manages approximately 1.1 million member lives, of these approximately 1 million are on a cost-risk basis.
CompCare’s infrastructure already in place to provide substance abuse/dependence disease management to accommodate nationwide third party reimbursement that we expect will be driven by positive outcomes from PROMETA pilots currently underway with managed care entities HealthNow New York Inc. and Horizon Blue Cross Blue Shield of New Jersey, and various criminal justice systems.
Capturing additional managed behavioral health revenues from initial disease management reimbursement on the high-utilizer subset of the substance dependent populations from CompCare’s existing managed care relationships. We currently estimate high-utilizers represent an average of 0.2% of plan lives. Further revenue growth within these plans would be expected based upon expanding penetration beyond this level into the broader substance dependent population, coupled with revenues from demonstrated medical savings. We also anticipate that there will be opportunities to provide add-on behavioral health disease management products, especially for disorders that commonly occur with substance abuse, which, in turn, will continue to increase our revenue base within these plans.
A substance dependence disease management infrastructure to accommodate initial treatment volumes from government and criminal justice systems and is expected to facilitate utilization and adoption of PROMETA by various managed care entities, criminal justice systems, self-insured employers, and government agencies.

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An immediate ability to provide access to treatment through CompCare’s provider network and infrastructure to managed lives for customers evaluating the system-wide adoption of the PROMETA protocols without the need for lengthy implementation cycles.
We will provide greater access to treatment with our patented protocols in the context of a disease management program, which integrates physiological, nutritional and psychosocial treatment, while concurrently coordinating the treatment of co-existing medical and behavioral disorders, resulting in a higher level of care for the individual patient.
We anticipate an acceleration of licensing new providers due to availability of reimbursement and the ability to increase private pay revenue growth through the licensing of provider networks.
     In November 2006, we announced that Horizon Blue Cross Blue Shield of New Jersey will conduct a commercial evaluation of the PROMETA protocols as a central component for substance dependence disease management. Horizon BCBSNJ has a total membership in excess of 3.2 million lives. Fifty patients will receive treatment with the PROMETA protocols for alcoholism, stimulants, and alcoholism and stimulants. Outcomes will be measured at ninety days, after which initial reimbursement may commence, with additional follow-up extending through six months.
     In January 2007, we announced that HealthNow New York Inc., the parent company of BlueCross BlueShield of Western New York and BlueShield of Northeastern New York, will conduct a commercial evaluation of the PROMETA protocols as a central component for substance dependence disease management. The pilot will take place in the chemical dependency unit of TLC Health Network, a HealthNow care provider. HealthNow has a total membership in excess of 720,000 lives. Fifty patients will receive treatment with the PROMETA protocols for alcoholism, stimulants, and poly-addiction to alcohol and stimulants. Outcomes will be measured at ninety days, with additional follow-up extending through six months. Endpoints that will be evaluated in the pilot include the ability to rapidly transition individuals back to their families and employers by converting their care to an out-patient treatment modality as soon as feasible.
Criminal Justice Systems and Government Agencies
     Drug and alcohol offenders impact all divisions of criminal justice including law enforcement, drug courts, probation, and correctional facilities. According to a Bureau of Justice Statistics Bulletin, “Prisoners in 2004,” published in October 2005, approximately 21% of the 1.2 million state and 55% of the 170,000 federal prisoners were convicted of drug offenses. A significant number of state and federal prisoners receive alcohol treatment in prison or during the re-entry period while under community supervision. The Office of National Drug Control Policy (ONDCP) estimates that more than 40% of the sentenced federal inmate population will have a diagnosable substance disorder that requires some type of drug abuse treatment program. City, county, state and federal criminal justice systems are in need of a more beneficial and convenient treatment alternative. More importantly, we will seek to work with local, state and federal criminal justice systems to intervene prior to incarceration or in conjunction with reentry programs with a goal of reducing the number of drug offenders admitted into prison.
     Drug courts first came to prominence in 1989 as a means to deal with the growing number of offenders involved with substance abuse. According to the National Drug Court Institute there were over 1,600 drug courts in 2004 located in all 50 states. Drug courts generally require participants to undergo treatment in lieu of incarceration. We will seek to engage and educate all parties (judges, attorneys, physicians, counselors, treatment providers) who influence the selection of the drug treatment programs and funding.
     We began to establish PROMETA as a covered treatment for city, state and county agencies in the public and criminal justice sectors in several states in 2006 and early 2007, building on outcomes data from the Dr. Urschel methamphetamine study and commercial pilot studies of the PROMETA protocols that were conducted in 2006.
     The PROMETA protocols for the treatment of methamphetamine and cocaine dependence were adopted as a treatment by Pierce County Alliance in 2006, based on the encouraging results of a pilot program. Pierce County

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Alliance began treating patients involved in the Pierce County criminal justice system in August 2006 and Pierce County Alliance is currently seeking additional funding from Pierce County and the state of Washington.
     The City Court of Gary adopted the PROMETA protocol after terminating its stimulant dependent pilot study prior to completion specifically because the interim results surpassed the Court’s historical success rates.
     We view the Pierce County Alliance and Gary Drug Court adoptions of the PROMETA protocols as important milestones and as references for our efforts in the criminal justice system. We believe the results of these and other pilots will serve as a template to increase adoption of the PROMETA protocols throughout the public and criminal justice systems of these states, as well as other states throughout the country. There are currently additional commercial pilots being conducted by treatment providers and courts in criminal justice populations in other states and we anticipate that additional pilots will commence in 2007.
Clinical Data from Research Studies
     A key to our success will be the publication of results from research studies evaluating treatment with the PROMETA protocols conducted by leading research institutions and preeminent researchers in the field of alcohol and substance abuse. Studies that are pending, underway or completed to date include:
A 90 patient multi-site, randomized double-blind placebo controlled study of the PROMETA protocols for the treatment of methamphetamine dependence conducted by Dr. Walter Ling of UCLA
A 60 patient randomized double-blind placebo-controlled study of the PROMETA protocol’s acute and immediate effects on cravings and cognition in alcohol dependent subjects designed and supervised by renowned alcoholism researcher, Dr. Joseph R. Volpicelli of the University of Pennsylvania, and conducted by the Institute of Addiction Medicine’s Dr. Jenny Starosta
An 84 patient randomized double-blind placebo-controlled study of the PROMETA protocol’s acute and immediate effects on cravings and cognition in methamphetamine dependent subjects designed and supervised by Dr. Harold Urschel, and conducted by Research Across America
A 60 patient randomized, double-blinded, placebo controlled study of the PROMETA protocol for the initiation, and extension of abstinence of alcoholism conducted by Dr. Raymond Anton at Medical University of South Carolina
A 30 patient open label randomized controlled study of the PROMETA protocols in the treatment of alcohol dependence conducted by Dr. Jeffery Wilkins at Cedars-Sinai Medical Center in Los Angeles
An 80 patient randomized double-blind placebo controlled study of the PROMETA protocols’ acute and immediate effects on cravings and cognition in alcohol dependent subjects conducted by Dr. Jeffery Wilkins at Cedars-Sinai Medical Center in Los Angeles
A 50 patient open label study of the physiological component of the PROMETA protocol for methamphetamine dependence conducted by Dr. Harold Urschel that was completed in 2006, in which it was reported that more than 80% of study participants experienced a significant clinical benefit—measured through decrease in cravings, reduction of methamphetamine use and treatment retention—after treatment, with no adverse events
A 100 patient pharmacoeconomic study to be conducted by the Parallax Center in New York City to compare outcomes achieved with the PROMETA protocol for alcohol dependency to the treatment program’s current protocol.
     In February 2007, Sheryl Smith Ph.D., a leading researcher in the field of neurosteroids, provided evidence supporting a mechanism of action underlying our PROMETA protocols at the Neurobiology of Addiction Conference. Dr. Smith presented data from her research on methamphetamine dependent rats, describing the

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methamphetamine induced increase in thea4 subunit of the GABAA receptor and the post-treatment decrease of this pathological marker, which has been associated with states of hyper-excitability and anxiety. This receptor dysregulation and associated symptomatology has previously been associated with alcohol and neurosteroid withdrawal in animal studies, and suggests a common cause of cravings in substance dependent individuals.
     Dr. Urschel’s study, which is being followed up by a double-blind study, is significant, as we believe it provides formal third-party validation of PROMETA. Methamphetamine and cocaine dependence are top priorities at the state and drug court levels, and because of the similar pathophysiologies of these drugs, a treatment validated for one may be readily adopted for the other. The positive results anticipated from the above studies will further validate PROMETA as a recommended treatment option for alcohol and stimulant dependence, as well as serve to accelerate our growth.
International Operations
     We have received allowances, issuances or notices that patent grants are intended for inventions related to one or more of our protocols for the treatment of alcohol and stimulant dependence in Mexico, Australia, New Zealand, Singapore, South Africa, Russia, Ukraine and Europe. We intend to consider opportunities in these and other countries where our intellectual property is protected.
     In 2006, our Swiss foreign subsidiary signed PROMETA license and services agreements with three sites in Switzerland to serve the international market. The sites in Switzerland commenced operations in the first quarter of 2007. Other international operations to date have not yet been significant, consisting primarily of treatment of dependencies on a pilot basis, legal and other development and start up activities. We will continue to evaluate the success of these initial programs before we pursue additional international expansion.
Our Operations
     We commenced operations in July 2003 and signed our first licensing and administrative services agreement in November 2003. Under our licensing agreements, we provide physicians and other licensed treatment providers access to our PROMETA protocols, education and training in the implementation and use of the licensed technology and marketing support. We receive a fee for the licensed technology and related services generally on a per patient basis. As of December 31, 2006, we had licensing agreements with physicians, hospitals and treatment providers for approximately 61 sites throughout the United States, with 41 sites contributing to revenues in 2006. We continue to enter into agreements with additional healthcare providers to increase the availability of the PROMETA protocols. As revenues are generally related to the number of patients treated, key indicators of our financial performance will be the number of facilities and healthcare providers that license our technology, and the number of patients that are treated by those providers using our PROMETA protocols. Since July 2003, approximately 1,300 patients have completed treatment using our PROMETA protocols at our licensed sites, and in research studies and commercial pilots being conducted to study our protocols.
     We manage two PROMETA Centers opened by David E. Smith, M.D. in Southern California in December 2005 and San Francisco in January 2007 whose revenues and expenses are included in our consolidated financial statements, and license a third PROMETA Center opened by the Canterbury Institute in New Jersey in January 2007. Canterbury plans to open an additional PROMETA Center in South Florida in the second quarter of 2007.
     To date, primarily self-pay patients have been treated with the PROMETA protocols. We expect revenues from third party payers will increase as a result of successful pilot studies completed and currently underway with state programs, managed care providers and criminal justice systems to evaluate the results of using of the PROMETA protocols in their programs. Positive results from these studies will help in our efforts to increase third-party reimbursement for providers using our protocols. Furthermore, our association with CompCare will enable us to create synergies to facilitate the use of our PROMETA treatment protocols by managed care treatment providers and provide an infrastructure for our substance abuse disease management offerings.
     We do not operate our own healthcare facilities, employ our own treating physicians or provide medical advice or treatment to patients. We provide services and access to tools that physicians may use to treat their patients as they determine appropriate. The hospitals, licensed healthcare facilities, and physicians that contract for the use of

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our technology own their facilities or professional licenses, and control and are responsible for the clinical activities provided on their premises. Patients receive medical care in accordance with orders from their attending physicians. Physicians with license rights to use the PROMETA protocols exercise their independent medical judgment in determining the specific application of our protocols, and the appropriate course of care for each patient. Following the medical portion of the treatment procedure, physicians, local clinics and healthcare providers specializing in drug abuse treatment administer and provide the psychosocial component of the protocol.
Our Market
Substance dependence is a worldwide problem with prevalence rates continuing to rise despite the efforts by national and local health authorities to curtail its growth. Substance dependence disorders affect many people and have wide-ranging social consequences. In 20052006, an estimated 22.222.6 million Americans aged 12 and older suffered from alcohol or other forms of drug abuse or dependence, of which 3.94.0 million, or 17.6%17.7%, received some kind of treatment, according to the National Survey on Drug Use and Health published by the Substance Abuse and Mental Health Services Administration (SAMHSA), an agency of the U.S. Department of Health and Human Services. Furthermore, according to the survey, approximately 10.4 million Americans age 12 and older, or 4.3 percent% of the population, are reported as having tried methamphetamine, and the percentage of methamphetamine use characterized as abuse or dependence increased 57% from 2002 to 2005. Findings from the Treatment Episode Data Set 1994-2004 (TEDS) Highlights – 2006 published by SAMHSA’s Office of Applied Studies show that the proportion of hospital admissions for primary abuse of methamphetamine as a percent of substance abuse treatment admissions increased from 2%2.5% in 19941996 to 7%8.3% in 2004.2006.

Summarizing data from the Office of National Drug Control Policy (ONDCP) and the National Institute on Alcohol Abuse and Alcoholism (NIAAA), the economic cost of alcohol and drug abuse exceeds $365 billion annually in the U.S., including $42 billion in healthcare costs and approximately $245 billion in productivity losses. Despite these staggering figures, it is a testament to the unmet need in the market that only 17.7% of those who need


treatment actually receive help. Traditional treatment methods are often not particularly effective, especially when it comes to those who are dependent on stimulants.

There are approximately 13,000 facilities reporting to SAMHSA that provide substance abuse treatment on an inpatient or outpatient basis. Historically, the disease of substance dependence has been treated primarily through behavioral intervention, with fairly high relapse rates. SAMHSA’s TEDS 2004 report states that in 2004 only 70% of those treated for alcoholism and 54% of those treated for cocaine completed detoxification, and that alcohol and cocaine outpatient treatment completion rates were only 46% and 27%, respectively.

Pharmacological options for alcohol dependence exist and a number of pharmaceutical companies have introduced or announced drugs to treat alcohol dependence. These drugs may require chronic or long-term administration. In addition, several of these drugs are generally not to be used until the patient has already achieved abstinence, are generally administered on a chronic or long-term continuing basis, and do not represent an integrated treatment approach to addiction. We believe PROMETA can be used at various stages of recovery, including initiation of abstinence and during early recovery, and can also complement other existing treatments. As such, our treatment programs offer a potentially valuable alternative or addition to traditional treatment methods.

It is commonly reported that addiction to methamphetamine is an epidemic rapidly spreading throughout the U.S.United States. Methamphetamine addicts are highly resistant to treatment and, even after intervention, relapse at very high rates.  Methamphetamine use is also spreading to the workplace.  A study funded by the Wal-Mart Foundation in 2004 determined that each methamphetamine-using employee costs his or her employer $47,500 per year in terms of lost productivity, absenteeism, higher healthcare costs and higher workers’ compensation costs.  For city, state and county governments and their taxpayers, methamphetamine abuse causes legal, medical, environmental and social problems. A study entitled “The Criminal Effect of Meth on Communities” conducted in 2005 by the National Association of Counties, which surveyed 500 counties in 45 states, reported that 58% of counties surveyed reported methamphetamine as their largest drug problem, with 87% reporting increases in arrests involving methamphetamine starting three years ago.earlier. Cocaine was reported as the number one drug problem in 19% of the counties. There are currently no generally accepted medical treatments for cocaine or methamphetamine dependence.
     Summarizing data from the ONDCP and the National Institute on Alcohol Abuse and Alcoholism (NIAAA), the economic cost of alcohol and drug abuse exceeds $365 billion annually in the U.S., including $42 billion in healthcare costs and approximately $245 billion in productivity losses. Despite these staggering figures, it is a testament to the unmet need in the market that only 17.6% of those who need treatment actually receive help. Traditional treatment methods are often not particularly effective, especially when it comes to those who are dependent on stimulants. Often faith, willpower, and counseling are the only options available. Compounding the lack of efficacious treatment options is the enormous stigma of leaving one’s life, income, and loved ones for weeks at a time to seek inpatient treatment.
     There are approximately 13,000 facilities reporting to SAMHSA that provide substance abuse treatment on an inpatient or outpatient basis. Historically, the disease of substance dependence has been treated primarily through behavioral intervention, with fairly high relapse rates. SAMHSA’s TEDS 2004 report states that in 2004 only 70% of those treated for alcoholism and 54% of those treated for cocaine completed detoxification, and that alcohol and cocaine outpatient treatment completion rates were only 46% and 27%, respectively. For patients who do complete treatment, the NIAAA reports relapse rates three months following treatment for alcohol dependence to be 50%. Relapse rates are higher for those suffering from cocaine dependence as opposed to alcohol. For the behavioral treatment of cocaine dependence, the Drug Abuse Treatment Outcome Study reports a relapse rate of 69% one year following outpatient treatment lasting 90 or fewer days and 80% one year following long-term residential treatment lasting 90 or fewer days.

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     Pharmacological options for alcohol dependence exist and a number of pharmaceutical companies have introduced or intend to introduce drugs to treat alcohol dependence. These drugs may require chronic or long-term administration. In addition, several of these drugs are generally not to be used until the patient has already achieved abstinence, are generally administered on a chronic or long-term continuing basis, and do not represent an integrated treatment approach to addiction.
Substance Dependence as a Disease

Scientific research indicates that not only can drugs interfere with normal brain functioning but can also have long-lasting effects that persist even after the drug is no longer being used. Data indicates that at some point changes may occur in the brain that can turn drug and alcohol abuse into substance dependence—a chronic, relapsing and sometimes fatal disease. Those dependent on drugs may suffer from compulsive drug craving and usage and be unable to stop drug use or remain drug abstinent without effective treatment. Professional medical treatment is often necessary to end this physiologically basedphysiologically-based compulsive behavior. We believe that addressing the physiological basis of substance dependence as part of an integrated treatment protocolprogram will improve clinical outcomes, reduce the cost of treating dependence, and reduce the cost to society by decreasing related criminality and violence and mitigating the costs associated with high risk behavior.
Methamphetamine
Methamphetamine

According to a National Institute on Drug Abuse (NIDA) research report “Methamphetamine: Abuse and Addiction” (January 2002), the effects of methamphetamine use can include addiction,memory loss, aggression, psychotic behavior and heart and brain damage. The damage to the brain caused by methamphetamine use isappears similar to damage caused by Alzheimer’s disease, stroke and epilepsy. Methamphetamine is highly addictive and users trying to abstain from use may suffer withdrawal symptoms that include depression, anxiety, fatigue, paranoia, aggression, and intense cravings for the drug. Chronic methamphetamine use can cause violent behavior, anxiety, confusion, and insomnia. Users can also exhibit psychotic behavior including auditory hallucinations, mood disturbances, delusions, and paranoia, possibly resulting in homicidal or suicidal thoughts. According to NIDA’s report, “Methamphetamine Linked to Long-Term Damage to Brain Cells” (March 2000), use of methamphetamine can cause damage to the brain that is detectable months after the use of the drug.
Alcohol


Alcohol

The Centers for Disease Control and Prevention rank alcohol the number three preventable cause of death in the United States, at 85,000with more than 75,000 deaths in 2000.annually. According to NIAAA, 44% of all deaths due to liver cirrhosis are alcohol related, with most of these deaths occurring in people 40 to 65 years old. One study found that 20 to 37% of all emergency room trauma cases involve alcohol use (Roizen, J., Alcohol and Trauma, 1988). Another study found that 46% of asymptomatic alcoholic men exhibited evidence of cardiomyopathy (Rubin, E., The Effects of Alcoholism on Skeletal and Cardiac Muscle, 1989).

The consequences of alcoholism and alcohol abuse affect most American families. One study estimated that 20-25% of all injury-related hospital admissions are the result of alcoholism or alcohol problems (Waller J., Diagnosis of Alcoholism in the Injured Patient, 1988). According to the National Commission Against Drunk Driving, nearly 600,000 Americans are injured in alcohol-related traffic crashes each year, resulting in 17,000 fatalities.

Cocaine and Crack Cocaine

Cocaine and crack use are societal problems that place a heavy load upon our criminal justice system. According to a Bureau of Justice Statistics Bulletin, “Prisoners in 2004,” published in October 2005, 55% of the 170,000 federal prisoners and 21% of the 1.2 million state prisoners were convicted of drug offenses. The National Institute of Justice reports that over 30% of all arrestees test positive for cocaine or crack.

The consequences of cocaine and crack use extend beyond the criminal justice system. NIDA reports the medical complications of cocaine use tocan include heart arrhythmias and heart attacks, chest pain, and respiratory

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failure, strokes, seizures and headaches, as well as abdominal pain and nausea. NIDA also notes that there have been no medications available to treat cocaine dependence.

Our Solution: PROMETA®Protocols Treatment Programs
     Those
People suffering from alcohol, cocaine or methamphetamine dependence have a clinical disease, but are often characterized as having a social disordersdisorder or a lack of self-discipline. In this context traditional treatment approaches have generally focused on the psychosocial aspect of the disease. While we believerecognize the psychological approach to substance dependence treatment is important, we recognizebelieve that a more comprehensive approach to this multi-factorial disease should be addressed as part of an integrated treatment approach intended to provide patients with an improved chance for recovery. We believe our integrated approach will offer patients an opportunity to achieve their individual recovery goals, and provide a sustainable commercial opportunity for our shareholders.goals.

Current research indicates that substance dependence is associated with altered cortical activity and changes in neurotransmitter function in the specific areas of the brain which are critical to normal brain function. Moreover, changes in the neurochemistry of the brain may underlie the hallmarks of substance dependence, including tolerance, withdrawal symptoms, craving, decrease in cognitive function and propensity for relapse. Our PROMETA protocolsTreatment Programs include medically directed and supervised treatments, prescription medications and nutritional supplements, combined with psychosocial or other recovery-oriented therapy. We provide a proprietary integrated treatment protocolprogram to medical professionals. The specific implementation of the protocolstreatment programs is at the discretion and judgment of the medical professionals providing care and tailored to individual patient needs.

The PROMETA treatment protocolsTreatment Programs provide for:

·      A comprehensive physical examination, including specific laboratory tests, prior to initiation of treatment by the treating physician, to determine if the patient is appropriate for the PROMETA protocol

·      Prescription medications delivered in a unique dosing algorithm

·      A nutritional plan and recommendations, designed to help facilitate and maintain the other aspects of recovery



·      One month of prescription medications and nutritional supplements following the initial treatment

·      Individualized psychosocial counseling or other recovery oriented counseling

The initiation of treatment under the PROMETA protocols involves the oral and intravenous administration of pharmaceuticals in a medically directed and supervised setting over a period of three days. The medications used in the PROMETA treatment protocolsTreatment Programs have been approved by the Food and Drug Administration (FDA) for uses other than treatment of substance dependence. Treatment generally takes place on an outpatient basis at a properly equipped outpatient setting or clinic, or at a hospital or other in-patient facility, by physicians and licensed healthcare providers who have licensed the rights to use our PROMETA protocols.Treatment Programs. The outpatient nature of the treatment provides the opportunity for the care to be provided in a discreet manner and without long periods away from home or work. The PROMETA protocolTreatment Program for stimulant dependence provides for a second, two-day administration at the facility, which takes place about three weeks after initiation. initiation of treatment. Following the initial three days, our protocolstreatment programs provide that patients receive one month of prescription medication, nutritional supplements, nutritional guidelines designed to assist in recovery, and individualized psychosocial or other recovery-oriented therapy.

Initial clinical observations by our licensed treatment providers suggestresults indicate that the PROMETA protocols may:
improve cognitive function
be associated with higher initial completion rates than conventional treatments
reduce cravings which can be a major factor in relapse
Treatment Programs may be associated with higher initial completion rates than conventional treatments, reduce cravings which can be a major factor in relapse and allow patients to more quickly engage in counseling or other forms of psychosocial therapy in a meaningful way.

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These initial conclusions have been reported in the treatment of approximately 1,300over 2,500 patients at licensed sites, commercial pilots and in research studies and commercial pilots being conducted to study our protocols. treatment programs. They may not be confirmed by formaladditional double-blind, placebo-controlled research studies, and may not be indicative of the long-term future performance of our protocols.treatment programs.

We believe the PROMETA protocolsTreatment Programs may offer an advantage to traditional alternatives for several reasons:

·      The PROMETA Treatment provided using the PROMETA protocols isPrograms are designed to address a spectrum of patient needs, including physiological, nutritional and psychological elements in an integrated way

·      The PROMETA treatment protocolsTreatment Programs include medically directed and supervised procedures designed to address neurochemical imbalances in the brain thought tothat may be caused or worsened by substance dependence. The rationale for thethis approach is that by addressing the underlying physiological balance thought to be disrupted by substance dependence, dependent persons may be better able to address the behavioral/psychological and environmental components of their disease

·      Treatment using the PROMETA protocolsTreatment Programs generally can be performed on an outpatient basis and dodoes not require long periods away from home or work

·      The PROMETA protocolsTreatment Programs may be initiated by physicians and treatment providers at various stages of recovery, including initiation of abstinence and during early recovery, and can complement other treatment modalities

Additionally, we provide training, education and other administrative services to assist physicians, healthcare providers and facilitiestreatment centers with staff education, marketing and administrative support.
Competition
Our Strategy

Our business strategy is to provide quality treatment programs that will become the standard-of-care for those suffering from alcoholism and other substance dependencies in a cost effective manner. We intend to grow our business through increased utilization from within existing and new licensees, additional managed treatment centers, and increased adoption of our PROMETA Treatment Programs and substance abuse disease management treatment approach by government agencies, criminal justice systems, managed care and other third-party payers.



Key elements of our business strategy include:

·      Providing our substance abuse disease management program to managed care health plans for reimbursement on a case rate or capitated basis, utilizing the CompCare infrastructure to provide some components of our services

·      Demonstrating the potential for improved clinical outcomes and cost effectiveness associated with using the PROMETA Treatment Programs, through commercial pilot studies with key managed care and other third-party payers

·      Expanding the base of our self-pay licensed treatment sites and managed treatment centers, focusing primarily on existing service areas

·      Seeking additional scientific and clinical research data to further validate the benefits of using the PROMETA Treatment Programs, through unrestricted grants for research studies by leading research institutions and preeminent researchers in the field of alcohol and substance abuse

·      Exploring opportunities in foreign markets

Disease Management

There are currently approximately 180 million lives in the United States covered by various managed care programs, including Preferred Provider Organizations (PPOs), Health Maintenance Organizations (HMOs), self-insured employers and managed Medicare/Medicaid programs. We believe our greatest opportunities for growth are in this market segment.

Our proprietary disease management programs are designed to improve treatment outcomes and lower the utilization of medical and behavioral health plan services by high utilizers and high risk enrollees.  Our disease management program includes the use of our PROMETA Treatment Programs, a proprietary information technology platform and database, predictive modeling, clinical algorithms, psychosocial programs, and integrated case management and coaching services. CompCare utilizes its infrastructure to provide many disease management services, including credentialing, peer review, monitoring, case management, coaching services, quality assurance and other standard behavioral healthcare services.

The proposed value proposition to our customers includes the following benefits:

·      Increased worker productivity, by reducing workplace absenteeism, compensation claims, and job related injuries

·      Decreased emergency room and inpatient utilization

·      Decreased readmission rates

·      Medical cost savings

We expect to gain leverage from our disease management program, which will allow us to market to managed care populations with one product and a relatively small, specialized sales force.  In addition, we believe that positive cost savings and clinical outcomes demonstrated in disease management with healthcare plans will provide a compelling motivation for speed of adoption by other health plans and other business sectors.


Self-pay Patients – Licensees

Our principal source of revenues to date has been from license fees derived from the licensing of our PROMETA Treatment Programs to physicians and other licensed treatment providers.  Although we plan to continue to provide such services to our existing licensees for the treatment of substance dependencies using our PROMETA Treatment Programs, we do not expect to significantly invest in or expand this line of business without positive returns on our investment. Accordingly, in 2008 we have significantly reduced our resources in each market area to more closely match our resources and expenditures with revenues from our licensees.

Managed Medical Practices and Treatment Centers

    Under the terms of full business service management agreements with medical professional corporations and treatment centers, we manage their business components and license the PROMETA Treatment Programs and use of our PROMETA trademark in exchange for management and licensing fees. These treatment centers offer the PROMETA Treatment Programs for dependencies on alcohol, cocaine and methamphetamines, and also offer medical interventions for other substance dependencies. Under generally accepted accounting principles, the revenues and expenses of such managed treatment centers are included in our consolidated financial statements. We currently manage two such treatment centers, the PROMETA Center in Santa Monica, California and Murray Hill Recovery in Dallas, Texas.

Criminal Justice Systems and Government Agencies

Drug and alcohol offenders impact all divisions of criminal justice including law enforcement, drug courts, probation, and correctional facilities.  A significant number of state and federal prisoners receive alcohol treatment in prison or during the re-entry period while under community supervision. ONDCP estimates that more than 40% of the sentenced federal inmate population will have a diagnosable substance disorder that requires some type of drug abuse treatment program. City, county, state and federal criminal justice systems are in need of a more beneficial and convenient treatment alternative.

We began to establish PROMETA as a covered treatment for city, state and county agencies in the criminal justice sectors in several states in 2006 and 2007.  We will continue to leverage existing pilots and programs with governmental agencies to provide adoption and funding by criminal justice, state and local government systems. However, while we have seen some early adoption, we will limit our investment in this sector due to the inherent inefficiencies we see at the present time in the public sector to adopt and implement our programs in a timely manner.

International Operations

We have received allowances, issuances or notices that patent grants are intended for inventions related to one or more of our treatment programs for the treatment of alcohol and stimulant dependence in the U.S., Mexico, Australia, New Zealand, Singapore, South Africa, Russia, Ukraine, South Korea, China and the European Union.  We will consider future opportunities in these and other countries where our intellectual property is protected.

We currently offer the PROMETA Treatment Program as well as other treatments for dependencies in Europe and Central America, and we plan to continue to expand in these markets.



Clinical Data from Research Studies

A key to our success will be the publication of results from research studies evaluating treatment with the PROMETA Treatment Programs conducted by leading research institutions and preeminent researchers in the field of alcohol and substance abuse. Studies funded by our unrestricted grants that are completed, pending or underway include:

Completed Studies

·      An 88-patient randomized, double-blind, placebo-controlled study of the PROMETA Treatment Program’s acute and immediate effects on cravings and cognition in methamphetamine dependent subjects designed and supervised by Harold Urschel, M.D., completed in October 2007.  Top line results showed a statistically significant reduction in cravings versus placebo.

·      A 50-patient open-label study of the physiological component of the PROMETA Treatment Program for methamphetamine dependence conducted by Dr. Urschel that was completed in 2006, in which it was reported that more than 80% of study participants experienced a significant clinical benefit—measured through decrease in cravings, reduction of methamphetamine use and treatment retention—after treatment, with no adverse events. The results of this study were reported in October 2007 in a peer-reviewed journal, Mayo Clinic Proceedings.

·      A 30-patient open label randomized controlled study of the PROMETA Treatment Programs in the treatment of alcohol dependence being conducted by Jeffery Wilkins, M.D., at Cedars-Sinai Medical Center in Los Angeles completed in August 2007. Top line results reported at 30 days showed a 94% decrease in median cravings and an 82% reduction in mean percentage of total drinking days.

·      
In February 2007, Sheryl Smith, Ph.D., a leading researcher in the field of neurosteroids, provided evidence supporting a mechanism of action underlying our PROMETA Treatment Programs at the Neurobiology of Addiction Conference.  Dr. Smith presented data from her research on methamphetamine dependent rats, describing the methamphetamine induced increase in the α4 subunit of the GABAA receptor and the post-treatment decrease of this pathological marker, which has been associated with states of hyper-excitability and anxiety.  This receptor dysregulation and associated symptomatology has previously been associated with alcohol and neurosteroid withdrawal in animal studies, and suggests a common cause of cravings in substance dependent individuals.

Pending Studies

·      An ongoing 60-patient randomized, double-blind, placebo-controlled study of the PROMETA Treatment Program’s acute and immediate effects on cravings and cognition in alcohol dependent subjects designed and being supervised by renowned alcoholism researcher, Joseph R. Volpicelli, M.D., of University of Pennsylvania, and conducted by Institute of Addiction Medicine’s Dr. Jenny Starosta.

·      An ongoing 90-patient multi-site, randomized, double-blind, placebo-controlled study of the PROMETA Treatment Programs for the treatment of methamphetamine dependence being conducted by Walter Ling, M.D., of UCLA.

·      An ongoing 60–patient, randomized, double-blind, placebo-controlled study of the PROMETA Treatment Program for the initiation and extension of abstinence of alcoholism being conducted by Raymond Anton, M.D., at Medical University of South Carolina.

·      An 80–patient, randomized, double-blind, placebo-controlled study of the PROMETA Treatment Programs’ acute and immediate effects on cravings and cognition in alcohol dependent subjects being conducted by Dr. Wilkins at Cedars-Sinai Medical Center.



Our Operations

Healthcare Services

We commenced operations in July 2003 and signed our first licensing and administrative services agreement in November 2003. Under our licensing agreements, we provide physicians and other licensed treatment providers access to our PROMETA Treatment Programs, education and training in the implementation and use of the licensed technology and marketing support. We receive a fee for the licensed technology and related services generally on a per patient basis. As of December 31, 2007, we had licensing agreements with physicians, hospitals and treatment providers for approximately 100 sites throughout the United States, with approximately 70 sites contributing to revenues in 2007.  We continue to enter into agreements with additional healthcare providers to increase the availability of the PROMETA Treatment Programs.  As revenues are generally related to the number of patients treated, key indicators of our financial performance will be the number of facilities and healthcare providers that license our technology, and the number of patients that are treated by those providers using our PROMETA Treatment Programs. Since July 2003, over 2,500 patients have completed treatment using our PROMETA Treatment Programs at our licensed sites, and in commercial pilots and research studies being conducted to study our treatment programs.

We currently manage two treatment centers, located in Santa Monica, California (The PROMETA Center, Inc.) and Dallas, Texas (Murray Hill Recovery, LLC), whose revenues and expenses are included in our consolidated financial statements.
    To date, a substantial portion of our healthcare services revenues has been derived from license fees for the use of the PROMETA Treatment Program in treating self-pay patients, and consolidation of self-pay patient revenues from managed treatment centers. We expect revenues from governmental agencies and other third party payers will increase as our PROMETA Treatment Program and disease management products are adopted and implemented by managed care providers, and state and county criminal justice systems. Furthermore, we believe additional positive results from published studies of our PROMETA Treatment Programs will enhance our efforts to increase third-party reimbursement for providers using our treatment programs.

We do not operate our own healthcare facilities, employ our own treating physicians or provide medical advice or treatment to patients. We provide services and access to tools that physicians may use to treat their patients as they determine appropriate. The hospitals, licensed healthcare facilities, and physicians that contract for the use of our technology own their facilities or professional licenses, and control and are responsible for the clinical activities provided on their premises. Patients receive medical care in accordance with orders from their attending physicians.  Physicians with license rights to use the PROMETA Treatment Programs exercise their independent medical judgment in determining the use and specific application of our treatment programs, and the appropriate course of care for each patient. Following the medical portion of the treatment procedure, physicians, local clinics and healthcare providers specializing in drug abuse treatment administer and provide the psychosocial component of the PROMETA Treatment Program.

Behavioral Health Managed Care Services

To date, all of our behavioral health managed care revenues have been derived from the operations of our consolidated subsidiary, CompCare, in which we acquired a majority controlling interest on January 12, 2007.

CompCare typically enters into contracts on an annual basis to provide managed behavioral healthcare and substance abuse treatment to clients’ members. Arrangements with clients fall into two broad categories: capitation arrangements, where clients pay CompCare a fixed fee per member per month, and fee-for-service and administrative service arrangements where CompCare may manage behavioral healthcare programs or perform various managed care services. Approximately 97% of CompCare’s revenues for the period January 13 through December 31, 2007 were derived from capitation arrangements. Under capitation arrangements, CompCare receives premiums from clients based on the number of covered members as reported by the clients. CompCare reviews membership eligibility records and other reported information to verify its accuracy in determining the amount of revenue to be recognized. The amount of premiums received for each member is fixed at the beginning of the contract term. These premiums may be subsequently adjusted, up or down, generally at the commencement of each renewal period.


For the period January 13 through December 31, 2007, 87% of behavioral health managed care services revenue was concentrated in contracts with six health plans to provide behavioral healthcare services under commercial, Medicare, Medicaid, and children’s health insurance plans (CHIP).  This includes a contract with a health plan to provide behavioral healthcare services to approximately 250,000 Medicaid recipients in Indiana, which represented approximately 40% of behavioral health managed care services revenue for the period January 13 through December 31, 2007. The term of each contract is generally for one year and is automatically renewable for additional one-year periods unless terminated by either party by giving the requisite written notice.

Competition

Healthcare Services

Our healthcare services business focuses on providing licensing, administrative and management services to licensees that administer PROMETA and other treatment programs, including managed treatment centers that are licensed and/or managed by us. We compete with many types of substance dependence treatment methods, treatment facilities and other service providers. Conventional forms of treatment for alcohol dependence are usually divided into phases: detoxification, which is typically conducted in medically directed and supervised environments; rehabilitation, which is often conducted through short- or long-term therapeutic facilities or programs, most of which do not offer medical management options; and relapse prevention/aftercare that is provided via structured outpatient treatment programs.

·      Detoxification, which is typically conducted in medically directed and supervised environments

·      Rehabilitation, which is often conducted through short- or long-term therapeutic facilities or programs, most of which do not offer medical management options

·      Relapse prevention/aftercare that is provided via structured outpatient treatment programs.

Most medically managed treatments require long-term usage of pharmaceuticals, resulting in low patient compliance. Conventional forms of treatment for stimulant dependence generally consist only of relapse prevention (psychosocial and recovery oriented therapy), conducted through therapeutic programs.  Regardless of the approach, there is great variability in the duration of treatment procedures, level of medical supervision, price to the patients and success rates.

One currently accepted practice for detoxifying patients from dependence on alcohol consists of heavily sedating the patient at an inpatient hospital facility for a period of 3 to 5 days. Due to the heavy sedation, the patient may need to be further observed for an additional 5 to 7 days. This procedure, while medically necessary to prevent severe complications, e.g. seizures or delirium tremens when withdrawing these patients from alcohol, does not consistently relieve the patient’s cravings or otherwise attempt to address the long term recovery of the patient. Further, the drugs typically used during this procedure (the most commonly utilized medications are Valium® (diazepam), Ativan® (lorazepam), and Xanax® (alprazolam)) can be addictive, require a time-intensive dose tapering and washout period, and may cause side effects.

While withdrawal from cocaine or methamphetamine dependence is not considered to be life threatening, withdrawal symptoms can be quiteextremely unpleasant and may lead to repeated relapses and treatment failures. Detoxification procedures typically involve the use of sedatives to assist patients through this difficult period. Following treatment, environmentally “cue induced” cravings, however, are especially pronounced and may re-occur for months to years.

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Treatment Programs

There are approximately 13,000 facilities reporting to the Substance Abuse and Mental Health Services Administration (SAMSHA)(SAMHSA) that provide substance dependence medical treatment services on an inpatient or outpatient basis. Well-known examples of residential treatment programs include the Betty Ford Center®, Caron Foundation®, Hazelden® and Sierra Tucson®. In addition, individual physicians may provide substance dependence treatment in the course of their practices. There appears to be no readily available reliable information about the success rates of these programs, nor agreed upon standards of how outcomes should be measured (e.g., self-reported abstinence or reduction in days of heavy drinking). Many of these traditional treatment programs have established name recognition, and their treatments may be covered in large part by insurance or other third party payers. To date, treatments using our protocolsPROMETA Treatment Programs have generally not been covered by insurance, and patients treated with the PROMETA protocolsTreatment Programs have been substantially self-pay patients.



Traditional treatment approaches for substance dependence focus mainly on group therapy, abstinence, and behavioral modification, while the disease’s underlying physiology and pathology is rarely addressed, resulting in fairly high relapse rates. Currently therapies are beginning to target brain receptors thought to play a central role in the disease process. We believe that our PROMETA protocolsTreatment Programs offer an improvement to traditional treatments because the integrated PROMETA protocolsTreatment Programs are designed to target the pathophysiology induced by chronic use of alcohol or other drugs in addition to nutritional and psychosocial aspects of substance dependence.  The abnormalities in brain function induced by chronic substance dependence may take weeks to years of drug abstinence to return to normal function, if at all. We believe the PROMETA protocolsTreatment Programs offer an advantage to traditional alternatives because they provide an integrated treatment methodology that is discreet, mildly sedating and that can be initiated in only three days, with a second two-day treatment three weeks later for addictive stimulants. Our PROMETA protocolsTreatment Programs also provide for one-monthone month of prescription medication and nutritional supplements, integrated with psychosocial or other recovery-oriented therapy.

We further believe the short initial outpatient treatment period when using our PROMETA protocolsTreatment Programs is a major advantage over traditional inpatient treatments and residential treatment programs, which typically consist of approximately 15 to 28 days of combined inpatient detoxification and recovery in a rehabilitation or residential treatment center. The PROMETA protocolsTreatment Programs do not require an extensive stay at an inpatient facility. Rather, the protocolstreatment programs offer the convenience of a three day treatment (addictive stimulants require a second two daytwo-day treatment three weeks later) and can generally be administered on an outpatient basis. This is particularly relevant since approximately 77%75% of adults classified with dependence or abuse are employed, and loss of time from work can be a major deterrent for seeking treatment.  Moreover, we believe the PROMETA protocolsTreatment Programs can be used at various stages of recovery, including initiation of abstinence and during early recovery, and can complement other forms of alcohol and drug abuse treatments. As such, our protocolstreatment programs offer a potentially valuable alternative or addition to traditional behavioral or pharmacotherapy treatments.

Treatment Medications

There are currently no generally accepted medical treatments for methamphetamine dependence. Anti-depressants and dopamine agonists have been investigated as possible maintenance therapies, but none have been FDA approved or are generally accepted for medical practice.

Several classes of pharmaceutical agents have been investigated as potential maintenance agents (e.g., anti-depressants and dopamine agonists) for cocaine dependence; however, none are FDA approved for treatment of cocaine dependence or widely generally accepted in medical practice. Their effects are variable in terms of providing symptomatic relief, and many of the agents may cause side effects or may not be well tolerated by patients.

There are a number of companies developing or marketing medications for reducing craving in the treatment of alcoholism. These include:

·      
The addiction medication naltrexone, an opiate receptor antagonist, is marketed by a number of generic pharmaceutical companies as well as under the trade name ReVia®, for treatment of alcohol dependence.dependence;

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·      However, naltrexone must be administered on a chronic or continuing basis and is associated with relatively high rates of side effects, including nausea.
Alkermes has developed and is marketing a long-acting injectable form
VIVITROL®, an extended release formulation of naltrexone VIVITROL®,manufactured by Alkermes, is intended to be administered by a physician via monthly injections. The companyinjections for the treatment of alcohol dependence in patients who are able to abstain from drinking in an outpatient setting and are not actively drinking prior to treatment initiation. Alkermes reported results from a phase III clinical study indicated that in clinical trials, when used in combination with psychosocial support, VIVITROL was shown to reduce the overall study population, patients treated with VIVITROL 380 mg experienced approximately a 25% reduction in the ratenumber of drinking days and heavy drinking relativedays and to placebo. Alkermes,prolong abstinence in partnership with Cephalon, made VIVITROL commercially available inpatients who abstained from alcohol the U.S. in June 2006.week prior to starting treatment;

·      
Forest Laboratories holds the license in the U.S. to market
Campral® Delayed-Release Tablets (acamprosate calcium), approved by the FDA in 2004. Acamprosate is an NMDA receptor antagonist. The product must beantagonist taken two to three times per day on a chronic or long-term basis.basis and marketed by Forest Laboratories.  Clinical studies supported the effectiveness in the maintenance of abstinence for alcohol-dependent patients who had undergone inpatient detoxification and were already abstinent from alcohol, but the product was not effective for patients who had not undergone detoxification and who were not abstinent prior to treatment.


studies supported the effectiveness in the maintenance of abstinence for alcohol-dependent patients who had undergone inpatient detoxification and were already abstinent from alcohol;

·      Topiramate (Topamax), a drug manufactured by Ortho-McNeill Jannssen, which is approved for the treatment of seizures. A multi-site clinical trial reported in October 2007 found that topiramate significantly reduced heavy drinking days in alcohol-dependent individuals.

Many medications marketed to treat alcohol or drug dependence are not administered until the patient is already abstinent, require long-term chronic administration andand/or must be taken several times a day to achieve the desired effect. As noted above, we believe the PROMETA protocolsTreatment Programs represent an integrated approach to treatment that includes medical, nutritional and psychosocial components that can be used at various stages of recovery, including initiation of abstinence and during early recovery, and can complement other existing treatments. As such, our protocolstreatment programs offer a potentially valuable addition to traditional medical treatment. Moreover, because treatment with the PROMETA protocolsTreatment Programs is an integrated treatment, we do not view the current medical therapies as directly competitive and in some cases may be used in conjunction with our protocols. We believe that the total cost of providing treatment using the PROMETA protocols falls within the typical range of prices for conventional treatment programs.  We also believe, based on the limited initial results discussed above, that treatment using our protocolstreatment programs may have higher completion rates, greater compliance, reduction or elimination of cravings, improved cognitive functioning and potentially lower relapse rates.

Behavioral Health Managed Care Services

The behavioral healthcare industry is very competitive and provides products and services that are price sensitive.  We believe that there are approximately 150 managed behavioral healthcare organizations (MBHOs) providing services for an estimated 227 million covered lives in the United States. CompCare’s competitors include both freestanding MBHOs as well as HMOs with internal behavioral health units or subsidiaries. Many of these competitors have revenues, financial resources, and membership substantially larger than CompCare. The extent of competition results in significant pricing pressures which limits CompCare’s revenue growth.  Accordingly, we expect CompCare’s future growth to come mainly from additional contracts.

In addition to MBHOs, there are disease management companies that may offer services or programs that will compete with our disease management products. We believe, however, that because our disease management programs are built around our proprietary, patented PROMETA Treatment Programs, no other company, MBHO or healthcare provider will be able to directly compete with our disease management product offering.

Development of Our Technology

Much of our proprietary, patented and patent patent–pending, substance dependence technology known as the PROMETA treatment protocols,Treatment  Program, was developed by Dr. Juan José Legarda, a European scientist educated at University of London who has spent most of his professional career conducting research related to substance abuse. Through his studies and research, Dr. Legarda identified some of the adverse physical effects of substance abuse on the brain and began to develop technologies that specifically focused on the neurochemistry of the brain as a core part of addictive behavior modification. In 2002, Dr. Legarda filed Patent Cooperation Treaty (PCT) applications in Spain to protect treatment protocolsprograms that he developed for dependencies to alcohol and cocaine. We acquired the rights to these patent filings in March 2003 through a technology purchase and license agreement with Dr. Legarda’s company, Tratamientos Avanzados de la Adiccion S.L., to which we pay a royalty of three percent of the amount the patient pays for treatment using our protocols.treatment programs. After acquiring these rights, we filed U.S. patent applications and other national phase patent applications based on the PCT filings, as well as provisional U.S. patent applications to protect aspects of additional treatment  protocolsprograms for alcohol, cocaine and other addictive stimulants.
     In December 2006, we announced that we received a Notice
We have two issued U.S. patents, one relating to the treatment of Allowance for Hythiam’s U.S. Patent for treating cocaine dependency from the United States Patent and Trademark Office. This patent represents a significant corporate milestone and we anticipate it will also serve to enhance protection of the intellectual property underlyingwith our PROMETA Protocols.
Treatment Program and one relating to our PROMETA Treatment Program for the treatment of certain symptoms associated with alcohol.  We have also received allowances, issuances or notices that patent grants are intended for our core intellectually property for the treatment of alcohol andand/or stimulant dependence in Mexico, Australia, New Zealand, Singapore, South Africa, Russia, Ukraine, South Korea, China and Europe.the European Union.


Once patents are issued, they generally will expire 20 years from the dates of original filing. Our two issued U.S. patents will expire in 2021.

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Proprietary Rights and Licensing

Our success depends upon a number of factors, includingin large part on our ability to protect our proprietary technology and operate without infringing on the proprietary rights of others. We rely on a combination of patent, trademark, trade secret and copyright laws and contractual restrictions to protect the proprietary aspects of our technology. To help ensure compliance with our license/joint venture agreements, we employ site managers in each of our major markets.  We have the followingOur branded trade names:names include the following:

·      
Hythiam®
Hythiam® logo
PROMETA®
PROMETA® logo
PROMETA Protocol™
PROMETA Protocols™
PROMETA Treatment Protocol™
PROMETA Treatment Protocols™
PROMETA Center®
PROMETA Centers™
PROMETA Treatment™
PROMETA Treatments™
·      
PROMETA®
·      
PROMETA Center®
·      
Catasys™  
·      
The Science of Recovery®

We impose restrictions in our protocol license agreements on our customers’ rights to utilize and disclose our technology. We also seek to protect our intellectual property by generally requiring employees and consultants with access to our proprietary information to execute confidentiality agreements and by restricting access to our proprietary information. We require that, as a condition of their employment, employees assign to us their interests in inventions, original works of authorship, copyrights and similar intellectual property rights conceived or developed by them during their employment with us.

Our Management Team

The following table sets forth information regarding our executive officers:

NamePositionAge
Terren S. PeizerChief Executive Officer4748
Richard A. AndersonSenior Executive Vice President3738
Christopher S. HassanSenior Executive Vice President4647
Anthony M. LaMacchiaSenior Executive Vice President5354
Chuck TimpeChief Financial Officer60
Sanjay SabnaniExecutive Vice President — Strategic Development    3661

Terren S. Peizeris the founder of our company and has served as our chief executive officer and chairman of theour board of directors since our inception in February 2003.  Mr. Peizer served as chief executive officer of Clearant, Inc. until October 2003,, a company which he founded in April 1999 to develop and commercialize a universal pathogen inactivation technology.technology, until October 2003. He served as chairman of its board of directors from April 1999 to October 2004 and as a director until February 2005. From February 1997 to February 1999, Mr. Peizer served as president and vice chairman of Hollis-Eden Pharmaceuticals, Inc., a Nasdaq Global Market listed company. In addition, from June 1999 through May 2003 he was a director, and from June 1999 through December 2000 he was chairman of the board, of supercomputer designer and builder Cray Inc., a Nasdaq Global Market company, and remains its largest beneficial stockholder. Since August 2006, he has served as chairman of the board of XCorporeal,Xcorporeal, Inc., an American Stock Exchange listed company. Mr. Peizer has been the largest beneficial stockholder and has held various senior executive positions with several technology and biotech companies. In these capacities, heHe has assisted these companies withby assembling management teams, boards of directors and scientific advisory boards, formulating business and financial strategies, and investor and public relations and capital formation.relations. Mr. Peizer has a background in venture capital, investing, mergers and acquisitions, corporate finance, and previously held senior executive

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positions with the investment banking firms Goldman Sachs, First Boston and Drexel Burnham Lambert. He received his B.S.E. in Finance from The Wharton School of Finance and Commerce.

Richard A. Andersonhas more than fifteen years of experience in business development, strategic planning and financial management. He has served as a director since July 2003 and an officer since April 2005. He was the chief financial officer of Clearant, Inc. from November 1999 until joining the company in March 2005, and served as a director from November 1999 to March 2006.  He served as chief financial officer of Intellect Capital Group from October 1999 through December 2001. From February through September 1999, he was an independent financial consultant. From August 1991 to January 1999, Mr. Anderson was previously with PriceWaterhouseCoopers, LLP, for seven


years, most recently a director and founding member of PriceWaterhouseCoopers Los Angeles Office Transaction Support Group, where he was involved in operational and financial due diligence, valuations and structuring for high technology companies. He received a B.A. in Business Economics from University of California, Santa Barbara.

Christopher S. Hassanis a senior healthcare executive who, prior to joining the companyus in July 2006, served as vice president, sales for Reckitt Benckiser Pharmaceuticals fromsince October 2003 until July 2006.2003. From 2000 to October 2002, he served as director of sales, North America for Drugabuse Sciences, Inc. a bio-pharmaceutical company. From 1996 to 2000, Mr. Hassan served as area business manager for Parke-Davis/Pfizer. From 1989 to 1996 he served as district sales manager for Bayer Pharmaceuticals. From 1986 to 1989, he was a director and vice president sales and acquisitions for Grammco Computer Sales. Mr. Hassan received a B.B.A. in Accounting from University of Texas, Austin.

Anthony M. LaMacchiais a senior healthcare executive who, prior to joining the companyus in July 2003, was the business development principal of GME Solutions, a healthcare financial consulting company providing Medicare graduate medical education and kidney acquisition cost recovery services, since October 2002. From November 1999 to April 2002, he was president & chief executive officer of Response Oncology, Inc., a diversified physician practice management company. He was recruited to this financially distressed company to direct a high-risk turnaround, and when continued market declines and debt covenant breaches compelled a bankruptcy filing, directed the company through all phases of the Chapter 11 process, the sale of all assets and the closure of its facilities. In June 1999, Mr. LaMacchia left Salick Health Care, Inc., which developed and operated outpatient cancer and kidney treatment centers and a clinical research organization engaging in pharmaceutical and clinical treatment trials, as executive vice president & chief operating officer, having started with the company as director of strategic planning & reimbursement in 1984. Previously, Mr. LaMacchia held positions of increasing responsibility with Blue Cross of California, Ernst & Young and Cedars-Sinai Medical Center. He is a certified public accountant who received his B.S. in Business Administration, Accounting from California State University, Northridge.

Chuck Timpeis a senior healthcare financial executive with over 35 years experience in the healthcare industry. Since March 1998, he has served as a director and since June 2002 as chairman of the Audit Committeeaudit committee for IPC-The Hospitalist Company, a $150$190 million physician specialty practice business.Nasdaq Global Market listed company. Prior to joining the companyus in June 2003, Mr. Timpe was chief financial officer, from its inception in February 1998, of Protocare, Inc., a clinical research and pharmaceutical outsourcing company which merged with Radiant Research, Inc. in March 2004, creating one of the country’s largest clinical research site management organizations. Previously, he was a principal in private healthcare management consulting firms he co-founded, chief financial officer of National Pain Institute, treasurer and corporate controller for American Medical International (now Tenet Healthcare Corp., an NYSE company)), and a member of Arthur Andersen, LLP’s healthcare practice, specializing in public company and hospital system audits. Mr. Timpe received his B.S. from University of Missouri, School of Business and Public Administration, and is a certified public accountant.
Sanjay Sabnani,prior to joining the company in April 2004, was acting director of business development and strategy at OSI Systems, Inc., where he was part of a senior team that delivered significant growth in revenues and market capitalization. Prior to joining OSI Systems, from May 1999 to December 2000, Mr. Sabnani was president and director at Venture Catalyst, Inc., where he spearheaded the company’s venture capital division, as well as managed the company’s web services business. Mr. Sabnani has authored or co-authored numerous articles and served as an expert speaker on topics as diverse as mergers and acquisitions, homeland security, entrepreneurship and internet strategy. He received his B.A. in English from University of California, Los Angeles.

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Financial Information about Segments

We currently operate in one reportableconduct our operations through two business segments: healthcare services and behavioral health managed care services. Our healthcare services segment focusedfocuses on providing licensing, administrative and management services to licensees that administer PROMETA and other treatment protocols,programs, including PROMETA Centersmanaged treatment centers that are licensed and/or managed by us. Substantially allOur behavioral health managed care services segment focuses on providing managed care services in the behavioral health, psychiatric and substance abuse fields, and principally includes the operations of our services are provided within the United States, and substantially allmajority-owned, controlled subsidiary, CompCare. A majority of our consolidated revenues and assets are earned or located within the United States.
     Beginning on January 12, 2007, our consolidated results will include the operations of CompCare, which will be presented in a separate reportable segment focused on providing managed care services.
Employees

    As of December 31, 2006,2007, we and our consolidated managed treatment centers employed approximately 120160 persons. In January 2008 we significantly reduced the number of employees in connection with streamlining our operations to focus on disease management and managed care, and we currently employ approximately 115 persons. We are not a party to any labor agreements and none of our employees are represented by a labor union. We anticipate hiring additional employees over the next year to execute our business strategy and meet our growth expectations.



Our Offices

We are incorporated under the laws of the State of Delaware. Our principal executive offices are located at 11150 Santa Monica Boulevard, Suite 1500, Los Angeles, California 90025 and our telephone number is (310) 444-4300.

Company Information
 
We make our annual reports on Form 10-K, our proxy statement, our quarterly reports on Form 10-Q, our current reports on Form 8-K, and any amendments to these reports available free of charge through links on our corporate website as soon as reasonably practicable after such reports are filed with, or furnished to, the Securities and Exchange Commission (SEC). Our corporate website is located on the Internet at http://www.hythiam.com. These reports are not part of this report or incorporated by reference herein. The public may read and copy any materials we file with the SEC at the SEC’s Public Reference Room at 100 F Street, NE, Washington, DC 20549. The public may obtain information on the operation of the Public Reference Room by calling the SEC at 1-800-SEC-0330. Additionally, the SEC maintains an Internet site that contains reports, proxy and information statements, and other information regarding issuers that file electronically with the SEC, which can be found at http://www.sec.gov.

ITEM 1A.  RISK FACTORS

You should carefully consider and evaluate all of the information in this report, including the risk factors listed below. Risks and uncertainties in addition to those we describe below, that may not be presently known to us, or that we currently believe are immaterial, may also harm our business and operations. If any of these risks occurs, our business, results of operations and financial condition could be harmed, the price of our common stock could decline, and future events and circumstances could differ significantly from those anticipated in the forward-looking statements contained in this report.

Risks related to our business

We have a limited operating history, and expect to continue to incur operating losses, making it difficult to evaluate our future prospects

We have been unprofitable since our inception in 2003 and expect to continue to incur substantial additional operating losses and negative cash flow from operations for at least the next twelve months.  AsWhile we continuecurrently estimate that our existing cash, cash equivalents and marketable securities will be sufficient to grow,fund our historical operationsoperating expenses and financial information are not necessarily indicative of our future operating results, financial conditioncapital requirements for at least the next two years or ability to operate profitably as a commercial enterprise. We may not be able tountil we achieve positive cash flows, before our existingthere can be no assurance this will be the case.  If cash reserves are expended. Revenues may not increase as quickly as anticipated, and changes in our business strategy, technology development or marketing plans or other events affecting our operating plans and expenses may result in the expenditure of existing cash before we achieve positive cash flow. If this occurs,insufficient to sustain us to profitability, our ability to meet our cash obligations as they become due and payable willmay depend on our ability to delay or reduce operating expenses, sell additional securities, borrow funds or some combination thereof. We may seek additional funding through public or private

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financing or through collaborative arrangements with strategic partners. We may also seek to raise additional capital through public or private financing in order to increase the amount of our cash reserves on hand. We may not be successful in raising necessary funds on acceptable terms, or at all.  If this occurs, we may be unable to meet our cash obligations as they become due and we may be required to delay or reduce operating expenses and curtail our operations, which would have a material adverse effect on us.

In addition, because of the significant publicly held minority interest in CompCare, we do not anticipate receiving dividends from CompCare or otherwise having access to cash flows generated by CompCare's business.  Although we do not anticipate advancing any funds to CompCare to fund its operations, you also should assume that we will not have access to cash generated by CompCare to fund the growth of our PROMETA-based business.

We may fail to successfully manage and maintain the growth of our business, which could adversely affect our results of operations, financial condition and business

Continued expansion could put significant strain on our management, operational and financial resources. The need to comply with the rules and regulations of the SEC and The NasdaqNASDAQ Global Market will continue to


place significant demands on our financial and accounting staff, financial, accounting and information systems, and our internal controls and procedures, any of which may not be adequate to support our anticipated growth. We may not be able to effectively hire, train, retain, motivate and manage required personnel. Our failure to manage growth effectively could limit our ability to satisfy our reporting obligations, or achieve our marketing, commercialization and financial goals.

In January 2007 we acquired a controlling equity interest in CompCare, a publicly traded company, and our ability to oversee this business, which is a new business for us and one with which we have had little previous experience, may significantly exacerbate the strain on our resources.

We may need additional funding, and we cannot guarantee that we will find adequate sources of capital in the future.

We have incurred negative cash flows from operations since inception and have expended, and expect to continue to expend, substantial funds to grow our business. Although we currently estimate that our existing cash, cash equivalents and marketable securities will be sufficient to fund our operating expenses and capital requirements for at least the next twelve months, we cannot assure you that we will not require additional funds before we achieve positive cash flows. We have based this estimate on assumptions that may prove to be wrong. Our existing cash, cash equivalents and marketable securities may not be sufficient to fund our business until we can become cash flow positive and we may never become cash flow positive.

If we raise additional funds by issuing equity securities, such financing will result in further dilution to our stockholders. Any equity securities issued also may provide for rights, preferences or privileges senior to those of holders of our common stock. If we raise additional funds by issuing additional debt securities, these debt securities would have rights, preferences and privileges senior to those of holders of our common stock, and the terms of the debt securities issued could impose significant restrictions on our operations. If we raise additional funds through collaborations and licensing arrangements, we might be required to relinquish significant rights to our technology or products, or to grant licenses on terms that are not favorable to us.

We do not know whether additional financing will be available on commercially acceptable terms when needed. If adequate funds are not available or are not available on commercially acceptable terms, we may need to downsize or halt our operations and may be unable to continue developing our products.

Our investments in adjustable rate securities are subject to risks which may cause losses and affect the liquidity of these investments.

As of December 31, 2007, approximately $19 million of our marketable securities consisted of auction rate securities, which are variable-rate instruments with longer stated maturities whose interest rates are reset at predetermined short-term intervals through a Dutch auction system. Through February 13, 2008, all of our auction rate securities held at December 31, 2007 had completed at least one auction successfully through the normal auction process, and we had reduced our total investments in auction rate securities to $11.5 million. However, from February 14 through March 12, 2008, auctions for these securities had failed, meaning the parties desiring to sell securities could not be matched with an adequate number of buyers, resulting in our having to continue to hold these securities. Although the securities are Aaa/AAA rated and collateralized by portfolios of student loans guaranteed by the U.S. government, based on current market conditions it is likely that auctions will continue to be unsuccessful, limiting the short-term liquidity of these investments until the auction succeeds, the issuer calls the securities, or they mature.  As a result, our ability to liquidate our investment and fully recover the carrying value of our investment in the near term may be limited or not exist. If the issuers are unable to successfully close future auctions or their credit ratings deteriorate, we may in the future record an impairment charge on these investments. In addition, these types of developments could cause us to reclassify our investments in auction rate securities from a current asset to a long-term asset. While we currently believe we will be able to liquidate our investment without significant loss within the next year and that these securities are not significantly impaired due to the government guarantee of the underlying securities, it could take until the final maturity of the underlying notes (up to 30 years) to realize our investments’ recorded value. Although we do not anticipate the potential lack of liquidity on these investments will affect our ability to execute our current business plan, based on our expected operating cash flows and our other sources of cash, there can be no assurance this will be the case.


Our treatment protocolsprograms may not be as effective as we believe them to be, which could limit our revenues and adversely affect our business

Our belief in the efficacy of our treatment protocolsPROMETA Treatment Programs is based on a limited number of studies and commercial pilots that have been conducted to date, and our initial experience with a relatively small number of patients. Such results may not be statistically significant, have not been subjected to close scientific scrutiny, and may not be indicative of the long-term future performance and safety of treatment with our protocols.programs. Controlled scientific studies, including those that have been announced and planned for the future, may yield results that are unfavorable or demonstrate that treatment with our protocolsprograms is not clinically effective or safe. If the initially indicated results cannot be successfully replicated or maintained over time, utilization of our protocolsprograms could decline substantially.

Our protocolsPROMETA Treatment Programs may not become widely accepted, which could limit our growth

Further marketplace acceptance of our protocolstreatment programs may largely depend upon healthcare providers’ and third-party payers’ interpretation of our limited data, the results of pending studies, or upon reviews and reports that may be given by independent researchers. In the event such research does not establish our treatment technologyprograms to be safe and effective, it is unlikely we will be able to achieve widespread market acceptance.

Disappointing results for our PROMETA Treatment Programs, or failure to attain our publicly disclosed milestones, could adversely affect market acceptance and have a material adverse effect on our stock price

There are a number of studies, evaluations and pilot programs currently in progress that are evaluating our PROMETA Treatment Programs, and we expect results of many to become available throughout the remainder of 2008 and during 2009.  Disappointing results or termination of evaluations or pilot programs could have a material adverse effect on the commercial acceptance of the PROMETA Treatment Programs and on our results of operations.  In addition, announcements regarding results, or anticipation of results, may increase volatility in our stock price. On October 24, 2007, the Pierce County Council in the State of Washington voted to end funding for PROMETA. This announcement had an immediate negative effect on our stock price, and we are unable to assess the longer term impact on our business. In addition to numerous upcoming milestones, from time to time we provide financial guidance and other forecasts to the market.  While we believe that the assumptions underlying projections and forecasts we make publicly available are reasonable, projections and forecasts are inherently subject to numerous risks and uncertainties.  Any failure to achieve milestones, or to do so in a timely manner, or to achieve publicly announced guidance and forecasts, could have a material adverse effect on our results of operations and the price of our common stock.

Our industry is highly competitive, and we may not be able to compete successfully

The healthcare business in general, and the substance dependence treatment business in particular, are highly competitive. We compete with many types of substance dependence treatment methods, treatment facilities and other service providers, many of whom are more established and better funded than we are. Many of these other treatment methods and facilities are well established in the same markets we target, have substantial sales volume, and are provided and marketed by companies with much greater financial resources, facilities, organization, reputation and experience than we have. The historical focus on the use of psychological or behavioral therapies, as opposed to medical or physiological treatments for substance dependence, may create further resistance to penetrating the substance dependence treatment market.

There are a number of companies developing or marketing medications for reducing craving in the treatment of alcoholism, including:

·      The
the addiction medication naltrexone, an opiate receptor antagonist, is marketed by a number of generic pharmaceutical companies as well as under the trade name ReVia®, for treatment of alcohol dependence.dependence;

·      
VIVITROL®, a long-acting injectable forman extended release formulation of naltrexone manufactured by Alkermes, is intended to be administered by a physician via monthly injections. Alkermes reported results from a phase III clinical study indicating thatinjections for the treatment of alcohol dependence in the overall study population, patients experienced approximately a 25% reduction in the rate of heavy drinking relative to placebo.


patients who are able to abstain from drinking in an outpatient setting and are not actively drinking prior to treatment initiation. Alkermes reported that in clinical trials, when used in combination with psychosocial support, VIVITROL was shown to reduce the number of drinking days and heavy drinking days and to prolong abstinence in patients who abstained from alcohol the week prior to starting treatment;

·      
Campral® Delayed-Release Tablets (acamprosate calcium), an NMDA receptor antagonist taken two to three times per day on a chronic or long-term basis.basis and marketed by Forest Laboratories.  Clinical studies supported the effectiveness in the maintenance of abstinence for alcohol-dependent patients who had undergone inpatient detoxification and were already abstinent from alcohol.alcohol;

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·      Topiramate (Topamax), a drug manufactured by Ortho-McNeill Jannssen, which is approved for the treatment of seizures. A multi-site clinical trial reported in October 2007 found that tropiramate significantly reduced heavy drinking days in alcohol-dependent individuals.

Our competitors may develop and introduce new processes and products that are equal or superior to our protocolsprograms in treating alcohol and substance dependencies. Accordingly, we may be adversely affected by any new processes and technology developed by our competitors.

There are approximately 13,000 facilities reporting to the Substance Abuse and Mental Health Services Administration that provide substance abuse treatment on an inpatient or outpatient basis. Well known examples of residential treatment programs include the Betty Ford Center®Center®, Caron Foundation®Foundation®, Hazelden®Hazelden® and Sierra Tucson®Tucson®. In addition, individual physicians may provide substance dependence treatment in the course of their practices.

We depend on key personnel, the loss of which could impact the ability to manage our business

Our future success depends on the performance of our senior management, and our key professional personnel, in particular our Chairman and Chief Executive Officer, Terren S. Peizer, our Senior Executive Vice Presidents, Richard A. Anderson, Anthony LaMacchia and Christopher S. Hassan and Anthony M. LaMacchia, and our Chief Financial Officer, Chuck Timpe. Each of these key executivesMessrs. Peizer, Hassan and Anderson each is party to an employment agreement which, subject to termination for cause or good reason, has a remaining term of sevenapproximately six, two and one years, respectively. Messrs. Timpe and LaMacchia do not have employment contracts.

CompCare's operations are highly dependent on the efforts of its senior management, in particular its President and Chief Executive Officer, John M. Hill, and Chief Financial Officer, Robert J. Landis. Each is party to an employment agreement which, subject to termination for cause or good reason, has a remaining term of approximately three years and eighteen months, to 3.5 years. respectively.

The loss of the services of Mr. Peizer or any other key member of management could have a material adverse effect on our ability to manage our business.

We are subject to personal injury claims,litigation, which could result in substantial liabilities that may exceed our insurance coverage

All significant medical treatments and procedures, including treatment utilizing our protocols,programs, involve the risk of serious injury or death. Even under proper medical supervision, withdrawal from alcohol may cause severe physical reactions. While we have not been the subject of any such claims, our business entails an inherent risk of claims for personal injuries and substantial damage awards. We cannot control whether individual physicians will apply the appropriate standard of care, or conform to our protocolstreatment programs in determining how to treat their patients. While our agreements typically require physicians to indemnify us for their negligence, there can be no assurance they will be willing and financially able to do so if claims are made. In addition, our license agreements require us to indemnify physicians, hospitals or their affiliates for losses resulting from our negligence.

CompCare is subject to lawsuits and claims of professional liability alleging negligence in performing utilization review and other managed care activities, and in the denial of payment for services. Such incidents may


result in professional negligence or other claims against CompCare causing it to incur fees and expend substantial resources in defense of such actions.

We currently have insurance coverage for up to $5 million per year, in the aggregate, for personal injury claims. Hythiam and CompCare maintain directors’ and officers’ liability insurance coverage, subject to a $100,000 per claim self insured retention.  CompCare maintains a program of insurance coverage against a broad range of risks related to its business, subject to deductibles and self-insured retentions. We may not be able to maintain adequate liability insurance at acceptable costs or on favorable terms. We expect that liability insurance will be more difficult to obtain and that premiums will increase over time and as the volume of patients treated with our protocolsprograms increases. In the event of litigation, regardless of its merit or eventual outcome, we may sustain significant lossesdamages or settlement expense (regardless of a claim's merit), litigation expense and significant harm to our operating capital.reputation.

If government and third-party payers fail to provide coverage and adequate payment rates for treatment using our protocols,treatment programs, our revenue and prospects for profitability will be harmed

Our future revenue growth will depend in part upon the availability of reimbursement for treatment using our protocolsprograms from third-party payers such as government health programs including Medicare and Medicaid, managed care providers, private health insurers and other organizations. Third-partyTo date, we have received an insignificant amount of revenue from our PROMETA Treatment Programs from governmental payers, managed care organizations and other third-party payers, and acceptance of our PROMETA Treatment Programs is important to the future prospects of our business. In addition, third-party payers are increasingly attempting to contain healthcare costs, and may not cover or provide adequate payment for treatment using our protocols.programs. Adequate third-party reimbursement might not be available to enable us to realize an appropriate return on investment in research and product development, and the lack of such reimbursement could have a material adverse effect on our operations and could adversely affect our revenues and earnings.

Our international operations may be subject to foreign regulation, and the success of our foreign operations will depend on many factors

The criteria of foreign laws, regulations and requirements are often vague and subject to change and interpretation. Our international operations may become the subject of foreign regulatory, civil, criminal or other investigations or proceedings, and our interpretations of applicable laws and regulations may be challenged. The defense of any such challenge could result in substantial cost and a diversion of management’s time and attention, regardless of whether it ultimately is successful. If we fail to comply with any applicable international laws, or a determination is made that we have failed to comply with these laws, our financial condition and results of operations, including our domestic operations, could be adversely affected.

In addition, the private pay healthcare system in Europe is not as developed as in the U.S and as a result it may be more difficult to convince patients in these countries to pay substantial amounts for treatment. We will be reliant on relationships that we establish with local companies, thought leaders and governments. There can be no

18


assurance we will be able to establish these relationships, maintain them or that the partners will retain their influence in the market. It may take longer than we expect to commence operations or to operate our business at profitable levels as we do not have the established relationships and or knowledge of the regulations and business practices in the markets we are in or entering.

Our ability to utilize net operating loss carryforwards may be limited

As of December 31, 2007, we had net operating loss carryforwards (NOLs) of approximately $ 100 million for federal income tax purposes that will begin to expire in 2024. These NOLs may be used to offset future taxable income, to the extent we generate any taxable income, and thereby reduce or eliminate our future federal income taxes otherwise payable. Section 382 of the Internal Revenue Code imposes limitations on a corporation's ability to utilize NOLs if it experiences an ownership change as defined in Section 382.  In general terms, an ownership change may result from transactions increasing the ownership of certain stockholders in the stock of a corporation by more than 50 percent over a three-year period. In the event that an ownership change has occurred, or were to occur, utilization of our NOLs would be subject to an annual limitation under Section 382 determined by multiplying the value of our stock


at the time of the ownership change by the applicable long-term tax-exempt rate as defined in the Internal Revenue Code.  Any unused annual limitation may be carried over to later years.  We may be found to have experienced an ownership change under Section 382 as a result of events in the past or the issuance of shares of common stock upon a conversion of notes, or a combination thereof.  If so, the use of our NOLs, or a portion thereof, against our future taxable income may be subject to an annual limitation under Section 382, which may result in expiration of a portion of our NOLs before utilization.
Risks related to our acquisition of CompCare

We may not realize the expected benefits of the CompCare acquisition, and may not be able to successfully utilize CompCare’s infrastructure

We may not be successful in realizing the expected benefits of our license agreement with Comprehensive Care Corporation or the recent acquisition of a majority controlling interest in CompCare. Achieving the benefits of our relationship with CompCare will depend in part on our ability to successfully utilize CompCare’s infrastructure and integrating with the benefits of its operations and personnel in a timely and efficient manner. The process will divert management time and attention from our other business, and require the effective coordination of personnel, systems, applications, policies, procedures, business processes and operations. This, too, will be difficult, unpredictable, and subject to delay because of possible cultural conflicts and different opinions on technical decisions and business strategy. WeCompCare is engaged in a business with which we have little experience, and this may present additional challenges to us. Further, we may be unable to realize synergies between our PROMETA business and CompCare's managed behavioral healthcare business. CompCare may be unable to retain CompCare’sits key management, technical, sales and customer support personnel. If we cannot successfully coordinate our operations and personnel, we will not realize the expected benefits of our relationship.  In addition, because of the significant publicly held minority interest in CompCare, we may be unable to gain access to the cash flows for CompCare and may be unable to realize the same level of benefits that we might be able to realize if CompCare were a wholly-owned subsidiary of ours.

There may be ongoing legal challenges to our relationship with CompCare, which could adversely affect our results of operations
     There is legal expense and potential delay, risk and uncertainty due to the ongoing litigation seeking to enjoin our
On May 25, 2007, we entered into a Termination Agreement with CompCare terminating a proposed merger with CompCare and the acquisition of the remaining common stock of CompCare. There are potential legal and economic risks associated with attempting to proceed with our proposed merger with CompCare, as well as with terminating the merger agreement and continuing with our ongoing relationship as itsCompCare’s majority controlling shareholder, including challenges from public minority shareholders concerning the procedural and financial fairness of our existing agreements, and any future agreements or arrangement between us.  Current or future litigation may be expensive and time consuming, and may impede or restrict our ability to operate effectively, which could negativenegatively impact our results of operations.

Risks related to CompCare’s business

CompCare may not be able to accurately predict utilization of its full-risk contracts resulting in contracts priced at levels insufficient to ensure profitability
     Managed
CompCare's managed care operations are at risk for costs incurred to provide agreed upon levels of service. Failure to anticipate or control costs could have material, adverse effects on CompCare. ProvidingCompCare’s business. A very large percentage of CompCare's services are provided on a full-risk capitation basis which exposes CompCare to the additionalsignificant risk that contracts negotiated and entered into may ultimately be unprofitable if utilization levels require it to provide services at a cost in excess of the capitation rates CompCare receives for the services. The population CompCare began managing in 2007 for its large Indiana client had not been subject to managed care previously and consequently there was little historical utilization data upon which do not account for or factorto base initial pricing. Actual utilization experience has been greater than initial estimates, resulting in such utilization levels.higher claim costs and lower profit margins. Failure to manage its costs or achieve anticipated cost reductions in populations brought under management would have an adverse effect on CompCare’s financial results.


CompCare may be unsuccessful in profitably managing its new Indiana Medicaid contract, orand may not be able to meet specified performance measures that would allow it to receive an increase in the contract may be significantly more costly than anticipatedrate
     Compcare
    CompCare may be unsuccessful in managing its new Indiana Medicaid contract that started January 1, 2007, which now comprises approximately one-thirdprovided over 40% of its operating revenues.revenues in 2007. Providing services under a new contract for populations at risk that have not been managed before exposes CompCare to the risk it may be unprofitable. There is a limited historical basis for the actuarial assumptions about the utilization of benefits by members covered under this new managed care behavioral program, and premiums based on these assumptions may be insufficient to cover the benefits provided and CompCare may be unable to obtain offsetting rate increases. Contract premiums have been set based on anticipated significant savings and on types of utilization management that may not be possible, may cause disagreements with providers and divert management resources, which would have an adverse impact on CompCare’s financial results.  Claims expense equaled revenues for this contract for the year ended December 31, 2007. CompCare is negotiating and believes it will receive a rate increase effective January 1, 2008, provided it complies with monthly performance measures it believes it will meet.  Although CompCare believes it will meet these standards, any failure to comply with one or more of the measurement criteria will reduce CompCare's anticipated cash flow and profitability from this contract.

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CompCare’s existing and potential managed care clients operate in a highly competitive environment and may be subject to a higher rate of merger, acquisition and regulation than in other industries

CompCare typically contracts with small to medium sized HMOs which may be adversely affected by the continuing efforts of governmental and third party payers to contain or reduce the costs of healthcare through various means. Its clients may also determine to manage the behavioral healthcare benefits “in house” and, as a result, discontinue contracting with CompCare. Additionally, its clients may be acquired by larger HMOs, in which case there can be no assurance that the acquiring company would renew its contract.

Many of CompCare’s managed care company clients provide services to groups covered by Medicare, Medicaid or Children’s Health Insurance Program (CHIP) plans susceptible to annual changes in reimbursement rates and eligibility requirements that could ultimately affect CompCare

 As of MayDecember 31, 2006,2007, CompCare managed approximately 517,000over 900,000 lives in connection with behavioral and substance abuse services covered through eightMedicaid and CHIP and Medicaid programs in Texas, Medicare and Medicaid in Florida, Medicaid in California, Indiana and Michigan. Of the 517,000 covered lives, 127,000 are related to contracts terminating May 31, 2006.Michigan, and Medicare in Maryland and Pennsylvania. Any changes in Medicare, Medicaid and/or CHIP reimbursement could adversely affect CompCare through contract bidding and cost structures with the health plans impacted by such changes. Temporary reductions have previously had a negative impact on CompCare, and if implemented in the future could have a material, adverse impact on its operations. OtherIn addition, states in which CompCare operates may pass legislation that would reduce its revenue through changes in the reimbursement rates or in the number of eligible participants. CompCare may be unable to reduce its costs to a level that would allow it to maintain current gross margins specific to its Medicare, Medicaid and CHIP programs.

CompCare is dependent on its provider network to provide services to its members

CompCare contracts with providers as a means to assure access to behavioral health services for its members. Some providers could refuse to contract with CompCare, demand higher payments, or take other actions which could result in higher healthcare operating expenses. In addition, certain providers may have significant market position, which could cause disruption to provider access in a particular geographic area for CompCare’s members and affect its contractual requirements with its customers of maintaining an adequate network.

Because providers are responsible for claims submission, the timing of which is uncertain, CompCare must estimate the amount of claims incurred but not reported, and actual results may differ materially

CompCare’s costs of care include estimated amounts for claims incurred but not reported (IBNR). The IBNR is estimated using an actuarial paid completion factor methodology and other statistical analyses that it


continually reviews and adjusts, if necessary, to reflect any change in the estimated liability. These estimates are subject to the effects of trends in utilization and other factors. CompCare’s estimates of IBNR may be inadequate, which would negatively affect results of operations. Considerable variability is inherent in such estimates, its unpaid claims liability may be inadequate, and actual results may differ materially from the estimates reported.
As a result of CompCare’s dependence
CompCare is dependent on a limited number of customers, theand loss or reduction in business of any one of these customers, or a reduction in business from any one of them, could have a material adverse effect on its working capital and future results of operations

For the six monthsyear ended November 30, 2006, approximately 82% of CompCare’s operating revenue was concentrated in contracts with six health plans toDecember 31, 2007 CompCare provide behavioral healthcare services to the members of six health plans under commercial, Medicare, Medicaid, and CHIP plans. For the same period of the prior fiscal year,contracts that on a combined basis represented approximately 87% of CompCare’s operating revenue was concentrated in contracts with eight health plans.revenue. The terms of each contract isare generally for one year periods and isare automatically renewable for additional one-year periods unless terminated by either party by giving the requisite written notice. The loss of one or more of these clients, unless replaced by new business, would negatively affect the financial condition of CompCare. In the past, CompCare has experienced the loss of major customers.
The
CompCare may be unsuccessful in obtaining performance bonds or other security that is required by its existing or future clients, and consequently may lose clients

CompCare’s new Indiana client requires CompCare to maintain a performance bond in the amount of $1,000,000.  In addition, certain of CompCare’s other customers may require restricted cash accounts or other security with respect to its obligations to pay IBNR claims and claims not yet processed and paid.  Due to CompCare’s small size and financial condition, it may be unable to provide the security required by its client, which could result in the loss of a client or clients which would negatively affect CompCare’s financial condition.

CompCare’s industry is subject to extensive state and federal regulations, as well as diverse licensure requirements varying by state. Changes in regulationsstate, and regulation changes could adversely affect thecontract profitability of CompCare’s contracts or itsand ability to gain and retain clients or

CompCare is required to gain new customers
     CompCare holdshold licenses or certificates to perform utilization review and third party administrator (TPA) services in some states.certain states in which it does business. Additional utilization review or TPA licenses may be required in the future and CompCare may not qualify to obtain them. In many states, entities that assume risk under contract with licensed insurance companies or health plans have not been considered by state regulators to be conducting an insurance or HMO business. As a result, CompCare has not sought licensure as either an insurer or HMO in any state. If the regulatory positions of these states were to change, its business could be materially affected until such time as it is able to meet the regulatory requirements, if at all. Additionally, some states may determine to contract directly with companies such as CompCare for managed behavioral healthcare services in which case they may also require it to maintain financial reserves or net worth requirements that it may not be able to meet. Currently, CompCare cannot quantify the potential effects of additional regulation of the managed care industry, but such costs will have an adverse effect on CompCare’s future operations to the extent that they are not able to be recouped in future managed care contracts.

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CompCare has an annual seasonality inis subject to existing clients issuing RFPs for the usagemanagement of behavioral services currently being managed

CompCare’s clients are aware of the highly competitive nature of the industry, and its contracts with them frequently contain provisions allowing termination of the contract by either party without cause with 90 days written notice.   Consequently CompCare’s clients may request from CompCare and any of its provider network, and its financial results may suffercompetitors a request for proposal (RFP) for behavioral services currently managed by CompCare, putting CompCare at risk of losing a client or clients.  For example, during 2007 a major Texas client issued an RFP prior to the extentend of CompCare’s contract.  CompCare submitted a proposal but were not chosen to continue services, resulting in a significant reduction in revenue.  In addition, certain administrative and overhead costs continued to be incurred past the termination date.

CompCare is subject to intense competition that may prevent it cannot adequately manage periodsfrom gaining new customers or pricing its contracts at levels to achieve sufficient gross margins to ensure profitability

CompCare is continually pursuing new business. However, many of increased utilizationCompCare's competitors are significantly larger and better capitalized than CompCare and the smaller size and financial condition of CompCare
     Historically

has proved a deterrent to some prospective customers. Additionally, CompCare will likely have difficulty in matching the financial resources expended on marketing by its competitors. As a result, CompCare may not be able to successfully compete in its industry. CompCare's major competitors include Magellan Health Services, United Behavioral Health, ValueOptions, and APS Healthcare.

CompCare's sales cycle is long, which complicates its ability to predict its growth.

The sales and implementation process of CompCare's services is lengthy and requires CompCare's potential clients to commit time and other resources.  CompCare's sales cycle is unpredictable and has generally experienced increasedranged from 12 to 18 months from initial contact to an executed contract.  Accordingly, it may be difficult to replace any lost business quickly.

A failure of CompCare's information systems would significantly impair its ability to serve its customers and manage its business.
An effective and secure information system, available at all times, is vital to CompCare's health plan customers and their members.  CompCare depends on its computer systems for significant service and management functions, such as providing membership verification, monitoring utilization, duringprocessing provider claims, and providing regulatory data and other client and managerial reports. Although CompCare's computer and communications hardware is protected by physical and software safeguards, it is still vulnerable to computer viruses, fire, storm, flood, power loss, telecommunications failures, physical or software break-ins and similar events. CompCare does not have 100% redundancy for all of its fourth fiscal quarter, which comprisescomputer and telecommunications facilities. A catastrophic event could have a significant negative effect on CompCare's business, results of operations, and financial condition.
    CompCare also depends on a third party provider of application services for its core business application.  Any sustained disruption in their services to us would have a material effect on our business.
CompCare is subject to fines and penalties being assessed by its clients

Many of CompCare’s contracts contain provisions stating that if its clients are assessed penalties or fines by a regulatory agency due to CompCare’s noncompliance with a contractual requirement, CompCare will be responsible for paying the months of March, April and May, and lower utilization throughout the remainder of the year. Seasonal variation also impacts its costs of care during these months, generally havingassessed fine or penalty.  Though to date, no material fines have been assessed under such provisions, any future fines would have a negative impact on results of operations.

CompCare may be unsuccessful in renewing its gross marginsNCQA accreditation and operating profits duringmay lose customers who require such accreditation

NCQA accreditation is required by several of CompCare’s client contracts and is an important consideration to its prospective clients.  CompCare is periodically evaluated by NCQA to validate the fourth quarter.Company’s adherence to NCQA industry-accepted standards covering operational areas such as preventative care, utilization management, credentialing, member rights and responsibilities, and quality improvement.   Maintaining these quality standards and the NCQA accreditation are important considerations of our customers and prospective clients who are evaluated against similar standards. If CompCare is not successful in renewing its NCQA accreditation, this could result in the loss of a client or clients which would negatively affect CompCare’s financial condition.

Risks related to our intellectual property

We may not be able to adequately protect the proprietary treatment protocolsPROMETA Treatment Programs which are the core of our business

We consider the protection of our proprietary treatment protocolsPROMETA Treatment Programs to be critical to our business prospects. We obtained the rights to some of our most significant patent-pendingPROMETA technologies through a licensean agreement whichthat is subject to a number of conditions and restrictions, and a breach or termination of that agreement or the bankruptcy of any party to that agreement could significantly impact our ability to use and develop our technologies.  WeWhile we have two issued U.S. patents, one relating to the treatment of cocaine dependency with our PROMETA Treatment Program and one relating to our PROMETA Treatment Program for the treatment of certain symptoms associated with alcohol dependency, we currently have no issued U.S. patents covering our PROMETA protocolTreatment Program for the treatment of alcoholmethamphetamine dependency. The patent applications we have licensed or filed may not issue as patents, and any issued patents may be too narrow in scope to provide us with a competitive advantage. Our patent position is uncertain and includes complex factual and legal issues, including the existence of prior art that may preclude or limit the scope of patent protection. Issued patents will generally expire twenty years after they were first filed.their priority date.  Our two issued U.S. patents will expire in 2021. Further, our patents and pending applications for patents and other intellectual property have been pledged as collateral to secure our obligations to pay certain debts, and our default with respect to those obligations could result in the transfer of our patents to our creditor.  In the event of such a transfer, we may be unable to continue to operate our business.
     Examiners, competitors
Patent examiners may reject our patent applications and thereby prevent us from receiving more patents.  Competitors, licensees and others may institute challengeschallenge our patents and, if successful, our patents may be denied, subjected to reexamination, rendered unenforceable, or invalidated. The cost of litigation to uphold the validity of patents, and to protect and prevent infringement can be substantial. We may not be able to adequately protect the aspects of our treatment protocolsprograms that are not patented or have only limited patent protection. Furthermore, competitors and others may independently develop similar or more advanced treatment protocolsprograms and technologies, may design around aspects of our technology, or may discover or duplicate our trade secrets and proprietary methods.

To the extent we utilize processes and technology that constitute trade secrets under applicable laws, we must implement appropriate levels of security to ensure protection of such laws, which we may not do effectively. Policing compliance with our confidentiality agreements and unauthorized use of our technology is difficult. In addition, the laws of many foreign countries do not protect proprietary rights as fully as the laws of the United


States. While we have not had any significant issues to date, theThe loss of any of our trade secrets or proprietary rights which may be protected under the foregoing intellectual property safeguards may result in the loss of our competitive advantage over present and potential competitors. Our intellectual property may not prove to be an effective barrier to competition, in which case our business could be materially adversely affected.

Our pending patent applications disclose and claim various approaches to the use of the PROMETA Treatment Program.  There is no assurance that we will receive one or more patents from these pending applications, or that, even if we receive one or more patents, the patent claims will be sufficiently broad to create patent infringement liability for competitors using treatment programs similar to the PROMETA Treatment Programs.

Confidentiality agreements with employees, licensees and others may not adequately prevent disclosure of trade secrets and other proprietary information

In order to protect our proprietary technology and processes, we rely in part on confidentiality provisions in our agreements with employees, licensees, treating physicians and others. These agreements may not effectively prevent disclosure of confidential information and may not provide an adequate remedy in the event of unauthorized disclosure of confidential information. In addition, others may independently discover trade secrets and proprietary information. Costly and time-consuming litigation could be necessary to enforce and determine the scope of our proprietary rights, and failure to obtain or maintain trade secret protection could adversely affect our competitive business position. To date weWe have had three instances in which it was necessary to send a formal demand to cease and desist using our protocolsprograms to treat patients due to breach of confidentiality provisions in our agreements.agreements, and in one instance have had to file suit to enforce these provisions.

We may be subject to claims that we infringe the intellectual property rights of others, and unfavorable outcomes could harm our business

Our future operations may be subject to claims, and potential litigation, arising from our alleged infringement of patents, trade secrets or copyrights owned by other third parties. Within the healthcare, drug and bio-technology industry, establishedmany companies actively pursue infringement claims and litigation, which makes the entry of competitive products more difficult. We may experience claims or litigation initiated by existing, better-funded competitors.competitors and by other third parties. Court-ordered injunctions may prevent us from continuing to market existing products or from bringing new products to market and the

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outcome of litigation and any resulting loss of revenues and expenses of litigation may substantially affect our ability to meet our expenses and continue operations.

Risks related to our industry

Our policies and procedures may not fully comply with complex and increasing regulation by state and federal authorities, which could negatively impact our business operations

Our PROMETA Treatment Programs have not been approved by the Food and Drug Administration (FDA), and while the drugs incorporated in the PROMETA Treatment Program have been approved for other indications, they are not FDA approved for the treatment of alcohol or substance dependency. We have not sought, and do not currently intend to seek, FDA approval for the PROMETA Treatment Program.  It is possible that in the future the FDA could require us to seek FDA approval for the PROMETA Treatment Program.

The healthcare industry is highly regulated and continues to undergo significant changes as third-party payers, such as Medicare and Medicaid, traditional indemnity insurers, managed care organizations and other private payers increase efforts to control cost, utilization and delivery of healthcare services. Healthcare companies are subject to extensive and complex federal, state and local laws, regulations and judicial decisions. The U.S. Congress and state legislatures are considering legislation that could limit funding to our licensees and CompCare's clients.  In addition, the Food and Drug Administration (FDA),FDA regulates development, testing, labeling, manufacturing, marketing, promotion, distribution, record-keeping and reporting requirements for prescription drugs, medical devices and biologics. Other regulatory requirements apply to dietary supplements, including vitamins. Compliance with laws and regulations enforced by regulatory agencies who have broad discretion in applying them may be required for our protocolsprograms or other medical productsprograms or services developed or used by us. Many healthcare laws and regulations applicable to our business are complex, applied broadly and subject to interpretation by courts and government agencies. Increasing regulation,Regulatory, political and


legal action and pricing pressures could prevent us from marketing some or all of our products and services for a period of time or permanently. Our failure, or the failure of our licensees, to comply with applicable regulations may result in the imposition of civil or criminal sanctions that we cannot afford, or require redesign or withdrawal of our protocolsprograms from the market.

We may be subject to regulatory, enforcement and investigative proceedings, which could adversely affect our financial condition or operations

We maycould become the subject of regulatory, enforcement, or other investigations or proceedings, and our relationships, business structure, and interpretations of applicable laws and regulations may be challenged. The defense of any such challenge could result in substantial cost and a diversion of management’s time and attention. Thus,In addition, any such challenges could require significant changes to how we conduct our business. Any such challenge could have a material adverse effect on our business, regardless of whether it ultimately is successful. If determination is made that we have failed to comply with any applicable laws, our business, financial condition and results of operations could be adversely affected.

The promotion of our protocolstreatment programs may be found to violate federal law concerning “off-label”off-label uses of prescription drugs, which could prevent us from marketing our protocolsprograms

 TheGenerally, the Food, Drug, &and Cosmetic (FDC) Act, requires that a prescription drugsdrug be approved by FDA for a specific medical indication and promotion of dietary supplements for uses beyond those permitted by law maybefore the product can be treated as the unlawful promotion of drugs. Violations ofdistributed in interstate commerce.  Although the FDC Act may resultdoes not prohibit a doctor’s use of a drug for another indication (this is referred to as off-label use), it does prohibit the promotion of a drug product for an unapproved use. FDA also permits the non-promotional discussion of information related to off-label use in criminalthe context of scientific or civil penalties, including seizure and injunction.medical communications. Our protocols call fortreatment programs include the use of prescription drugs that have been approved by FDA, but not for the treatment of chemical dependence and drug addiction, conditions not approvedwhich is how the drugs are used in our programs. Although we carefully structure our communications in a way that is intended to comply with the FDC Act and FDA regulations, it is possible that our actions could be found to violate the prohibition on off-label promotion of drugs. In addition, the FDC Act imposes limits on the types of claims that may be made for use ina dietary supplement, and the drugs’ official labeling, andpromotion of a dietary supplement beyond such claims may also be seen as the unlawful promotion of a drug product for an unapproved use. Because our treatment programs also include the use of nutritional supplements. The promotionsupplements, it is possible that claims made for those products could also put us at risk of our protocols through advertising and other means may be found to violateFDA enforcement for making unlawful claims.

Violations of the FDC Act or FDA regulations can result in a range of sanctions, including administrative actions by FDA (such as issuance of a Warning Letter), seizure of product, issuance of an injunction prohibiting future violations, and imposition of criminal or the FDC Act.civil penalties. A successful enforcement action could prevent promotion of our protocolstreatment programs and we may be unable to continue operating under our current business model. TheEven if we defeat an enforcement action, the expenses associated with losing or defending a claim, ordoing so, as well as the negative publicity concerning the off-label“off-label” use of drugs in our protocols,treatment programs, could adversely affect our business and results of operation.

The FDA has recently increased enforcement efforts in the area of promotion of “off-label” use of drugs, and we cannot assure you that our business practices or third party clinical trials will not come under scrutiny.

Treatment using our protocolsprograms may be found to require FDA or other review or approval, which could delay or prevent the study or use of our protocolstreatment programs
     The
Under authority of the FDC Act, FDA asserts jurisdiction over manyextensively regulates entities and individuals engaged in the conduct of clinical trials, orwhich broadly includes experiments in which a drug is administered to humanhumans.  FDA regulations require, among other things, submission of a clinical trial treatment program for FDA review, obtaining from the agency an investigational new drug (IND) exemption before initiating a clinical trial, obtaining appropriate informed consent from study subjects, having the study approved and hospitals and clinics have establishedsubject to continuing review by an Institutional Review Boards (IRBs)Board (IRB), and reporting to review and approve clinical trials using investigational treatmentsFDA safety information regarding the conduct of the trial.  Certain third parties have engaged or are engaging in their facilities. Usethe use of our treatment protocolprogram and the collection of outcomes data in ways that may be considered to constitute a clinical trial, and that may be subject to FDA regulations and require IRB approval and oversight.  In addition, it is possible that use of our treatment program by individual physicians in treating their patients may be found to constitute a clinical trial or investigation that requires IRB review or submission of an IND


or is otherwise subject to regulation by FDA.  FDA investigational new drug (IND) exemption. The FDA may find that use of our protocols or collection of outcomes data constitutes ahas authority to inspect clinical investigation subjectsites and IRBs, and to IRBtake action with regard to any violations.  Violations of FDA regulations regarding clinical trials can result in a range of actions, including suspension of the trial, prohibiting the clinical investigator from ever participating in clinical trials, and FDA jurisdiction and may take enforcement action against us.criminal prosecution.  Individual hospitals and physicians may also submit their use of our protocols in treatment programs to their IRBs, which may prohibit or place restrictions on it.  Any of these results mayFDA enforcement actions or IRB restrictions could adversely affect our business and the ability of our customers to use our protocols.treatment programs.

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The FDA has recently increased enforcement efforts regarding clinical trials, and we cannot assure you that the activities of our customers or others using our treatment programs will not come under scrutiny.

Failure to comply with FTC laws or similar state laws could result in sanctions or limit the claims we can make

Our promotional activities and materials, including advertising to consumers and physicians,professionals, and materials provided to licensees for their use in promoting our protocols,treatment programs, are regulated by the Federal Trade Commission (FTC) under the FTC Act, which prohibits unfair and deceptive acts and practices, including claims which are false, misleading or inadequately substantiated. The FTC typically requires competent and reliable scientific tests or studies to substantiate express or implied claims that a product or service is safe or effective. If the FTC were to interpret our promotional materials as making express or implied claims that our protocolstreatment programs are safe or effective for the treatment of alcohol, cocaine or methamphetamine addiction, or any other claims, it may find that we do not have adequate substantiation for such claims. FailureAllegations of a failure to comply with the FTC Act or similar laws enforced by state attorneys general and other state and local officials could result in administrative or judicial orders limiting or eliminating the claims we can make about our protocols,treatment programs, and other sanctions including substantial fines.financial penalties.

Our business practices may be found to constitute illegal fee-splitting or corporate practice of medicine, which may lead to penalties and adversely affect our business

    Many states, including California in which our principal executive offices and twoone of our managed PROMETA Centers aretreatment centers is located, have laws that prohibit business corporations, such as us, from practicing medicine, exercising control over medical judgments or decisions of physicians, or engaging in arrangements with physicians such as employment, payment for referrals or fee-splitting, with physicians.fee-splitting.  Courts, regulatory authorities or other parties, including physicians, may assert that we are engaged in the unlawful corporate practice of medicine by providing administrative and ancillaryother services in connection with our protocols,treatment programs or by consolidating the revenues of the physician practices we manage, or that licensing our technology for a license fee that could be characterized as a portion of the patient fees, or subleasing space and providing turn-key business management to affiliated medical groups in exchange for management and licensing fees, constitute improper fee-splitting or payment for referrals, in which case we could be subject to civil and criminal penalties, our contracts could be found invalid and unenforceable, in whole or in part, or we could be required to restructure our contractual arrangements. If so, we may be unable to restructure our contractual arrangements on favorable terms, which would adversely affect our business and operations.

Our business practices may be found to violate anti-kickback, physician self-referral or false claims laws, which may lead to penalties and adversely affect our business

The healthcare industry is subject to extensive federal and state regulation with respect to financial relationships and “kickbacks”kickbacks involving healthcare providers, physician self-referral arrangements, filing of false claims and other fraud and abuse issues. Federal anti-kickback laws and regulations prohibit offers, payments, solicitations, or receipts of remuneration in return for (i) referring patients for items or services covered by Medicare, Medicaid or other federal healthcare programs, or (ii) purchasing, leasing, ordering or arranging for or recommending any service, good, item or facility for which payment may be made by a federal health care program. In addition, subject to numerous exceptions, federal physician self-referral legislation, commonly known as the Stark law, generally prohibits a physician from orderingreferring patients for  certain designated health services reimbursable by Medicare Medicaid or other federal healthcare programsMedicaid  from any entity with which the physician has a financial relationship, and many states have similaranalogous laws. Other federal and state laws govern the submission of claims for reimbursement, or false claims laws. One of the most prominent of these laws is the federal Civil False Claims Act, and violations of other laws, such as the federal anti-kickback lawslaw or the FDA prohibitions against promotion of off-label uses of drugs,


may also be prosecuted as violations of the Civil False Claims Act. CompCare provides services to health plans that could become involved with false claims, which could include allegations against CompCare as well.

Federal or state authorities may claim that our fee arrangements, agreements and relationships with contractors, hospitals and physicians violate these laws and regulations. Violations of these laws aremay be punishable by monetary fines, civil and criminal penalties, exclusion from participation in government-sponsored healthcare programs and forfeiture of amounts collected in violation of such laws. If our business practices are found to violate any of these provisions, we may be unable to continue with our relationships or implement our business plans, which would have an adverse effect on our business and results of operations.

We may be subject to healthcare anti-fraud initiatives, which may lead to penalties and adversely affect our business

State and federal governments are devoting increased attention and resources to anti-fraud initiatives against healthcare providers, takingand may take an expansive definition of fraud that includes receiving fees in connection with a healthcare business that is found to violate any of the complex regulations described above. While to our knowledge we have not been the subject of any anti-fraud investigations, if such a claim were made defending our business

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practices could be time consuming and expensive, and an adverse finding could result in substantial penalties or require us to restructure our operations, which we may not be able to do successfully.

Our use and disclosure of patient information is subject to privacy and security regulations, which may result in increased costs

In conducting research or providing administrative services to healthcare providers in connection with the use of our protocols,treatment programs, we may collect, use, disclose, maintain and transmit patient information in ways that will be subject to many of the numerous state, federal and international laws and regulations governing the collection, dissemination, use, anddisclosure, storage, transmission and/or confidentiality of patient-identifiable health information, including the administrative simplification requirements of the Health Insurance Portability and Accountability Act of 1996 and its implementing regulations (HIPAA). The HIPAA Privacy Rule restricts the use and disclosure of patient information, and requires safeguarding that information. The HIPAA Security Rule establishes elaborate requirements for safeguarding patient information transmitted or stored electronically.  HIPAA applies to covered entities, which may include most healthcare facilities and does include health plans that will contract for the use of our protocolsprograms and our services. The HIPAA rules require covered entities to bind contractors like us to compliance with certain burdensome HIPAA rule requirements known as business associate requirements. If we are providing management services that include electronic billing on behalf of a physician practice or facility that is a covered entity, we may be required to conduct those electronic transactions in accordance with the HIPAA regulations governing the form and format of those transactions (HIPAA Transactions Rule).  Other federal and state laws restricting the use and protecting the privacy and security of patient information also apply to our licensees directly and in some cases to us, either directly or indirectly. We may be required to make costly system purchases and modifications to comply with the HIPAA rule requirements that are imposed on us and our failure to comply may result in liability and adversely affect our business.

CompCare is subject to the administrative simplification requirements of HIPAA for most healthcare facilities and health plans that contract for the use of CompCare’s services.  The HIPAA Transactions Rule requires CompCare to comply with format and data content standards for common healthcare transactions on behalf of our licensees. The HIPAA Privacy Rule restricts the use and disclosure of patient information, and requires safeguarding that information. The HIPAA Security Rule establishes elaborate requirements for safeguarding patient information transmitted or stored electronically. Failure to comply may result in civil and criminal liability and penalties, and have a material adverse effect on CompCare’s ability to retain its customers or to gain new business.

Federal and state consumer protection laws are being applied increasingly by the FTC and state attorneys general to regulate the collection, use, storage, and disclosure of personal or patient information, through web sites or otherwise, and to regulate the presentation of web site content. Courts may also adopt the standards for fair information practices promulgated by the FTC, which concern consumer notice, choice, security and access. Numerous other federal and state laws protect the confidentiality and security of personal and patient information. Other countries also have, or are developing laws governing the collection, use, disclosure and transmission of personal or patient information and these laws could create liability for us or increase our cost of doing business.


Our business arrangements with health care providers may be deemed to be franchises, which could negatively impact our business operations

Franchise arrangements in the United States are subject to rules and regulations of the FTC and various state laws relating to the offer and sale of franchises.  A number of the states in which we operate regulate the sale of franchises and require registration of the franchise offering circular with state authorities and the delivery of a franchise offering circular to prospective franchisees.  State franchise laws often limit, among other things, the duration and scope of non-competitive provisions, the ability of a franchisor to terminate or refuse to renew a franchise and the ability of a franchisor to designate sources of supply.  Franchise laws and regulations are complex, apply broadly and are subject to interpretation by courts and government agencies.  Federal or state authorities or healthcare providers with whom we contract may claim that the agreements under which we license rights to our technology and trademarks and provide services violate these laws and regulations. Violations of these laws are punishable by monetary fines, civil and criminal penalties, and forfeiture of amounts collected in violation of such laws. If our business practices are found to constitute franchises, we could be subject to civil and criminal penalties, our contracts could be found invalid and unenforceable, in whole or in part, or we could be required to restructure our contractual arrangements.  We may be unable to continue with our relationships or restructure them on favorable terms, which would have an adverse effect on our business and results of operations.  We may also be required to furnish prospective franchisees with a franchise offering circular containing prescribed information, and restrict how we market to or deal with healthcare providers, potentially limiting and substantially increasing our cost of doing business.

Risks related to our common stock

Over 25% of our stock is controlled by our chairman and chief executive officer, who has the ability to substantially influence the election of directors and other matters submitted to stockholders

    Reserva Capital, LLC and Bonmore, LLC, whose sole managing member is our chairman and chief executive officer, beneficially own 13,700,000 shares of our common stock, which represent approximately 25.2% of our 54,387,604 shares outstanding. As a result, he has and is expected to continue to have the ability to significantly influence the election of our board of directors and the outcome of all other issues submitted to our stockholders. The interests of these principal stockholders may not always coincide with our interests or the interests of other stockholders, and they may act in a manner that advances his best interests and not necessarily those of other stockholders. One consequence to this substantial influence or control is that it may be difficult for investors to remove management of the company. It could also deter unsolicited takeovers, including transactions in which stockholders might otherwise receive a premium for their shares over then current market prices.

Our stock price may be subject to substantial volatility, and the value of your investment may decline

Our common stock is traded on The NasdaqNASDAQ Global Market, and trading volume may be limited or sporadic.  Over 2006,The market price of our common stock has experienced, and may continue to experience, substantial volatility. Over 2007, our common stock has traded between $4.77$2.68 and $9.35$10.21 per share, on volume ranging from approximately 18,00050,000 to 3.73 million shares per day.  As a result, the current price for our common stock on NasdaqNASDAQ is not necessarily a reliable indicator of our fair market value. The price at which our common stock will trade may be highly volatile and may fluctuate as a result of a number of factors, including the number of shares available for sale in the market, quarterly variations in our operating results and actual or anticipated announcements of pilots and scientific studies of the effectiveness of our PROMETA protocols,Treatment Programs, new products or services by us or competitors, regulatory investigations or determinations, acquisitions or strategic alliances by us or our competitors, recruitment or departures of key personnel, the gain or loss of significant customers, changes in the estimates of our operating performance, actual or threatened litigation, market conditions in our industry and the economy as a whole.
Over 30%
Volatility in the price of our common stock on the NASDAQ Global Market may depress the trading price of the common stock our common stock.  The risk of volatility and depressed prices of our common stock also applies to warrant holders who receive shares of common stock upon conversion.



Numerous factors, including many over which we have no control, may have a significant impact on the market price of our common stock, including:

·      announcements of new products or services by us or our competitors; current events affecting the political, economic and social situation in the United States and other countries where we operate;

·      trends in our industry and the markets in which we operate;

·      changes in financial estimates and recommendations by securities analysts;

·      acquisitions and financings by us or our competitors;

·      the gain or loss of a significant customer;

·      quarterly variations in operating results;

·      volatility in exchanges rate between the US dollar and the currencies of the foreign countries in which we operate;

·      the operating and stock price performance of other companies that investors may consider to be comparable; and

·      purchases or sales of blocks of our securities.
    Furthermore, stockholders may initiate securities class action lawsuits if the market price of our stock is controlleddrops significantly, which may cause us to incur substantial costs and could divert the time and attention of our management.

Future sales of common stock by existing stockholders, or the perception that such sales may occur, could depress our stock price

The market price of our common stock could decline as a single stockholder who hasresult of sales by, or the ability to substantially influence the electionperceived possibility of directorssales by, our existing stockholders.  We have completed a number of private placements of our common stock and other matters submittedsecurities over the last several years, and we have effective resale registration statements pursuant to stockholders
     As of December 31, 2006, Reserva Capital, LLC, whose sole managing member is Terren S. Peizer, our chairman and chief executive officer, beneficially owned 13,700,000which the purchasers can freely resell their shares which represent approximately 31%into the market.  In addition, most of our 43,917,000outstanding shares are eligible for public resale pursuant to Rule 144 under the Securities Act of 1933, as amended.  Approximately 15 million shares of outstandingour common stock are currently held by our affiliates and may be sold pursuant to an effective registration statement or in accordance with the volume and other limitations of Rule 144 or pursuant to other exempt transactions.  Future sales of common stock by significant stockholders, including those who acquired their shares in private placements or who are affiliates, or the perception that such sales may occur, could depress the price of our common stock. As a result, he has

Future issuances of common stock and is expected to continue to havehedging activities may depress the ability to determine or significantly influence the electiontrading price of our boardcommon stock

Any future issuance of directors andequity securities, including the outcomeissuance of all other issues submitted to our stockholders. The interestsshares upon exercise of this principal stockholder may not always coincide with our interests oroutstanding warrants, could dilute the interests of otherour existing stockholders, and itcould substantially decrease the trading price of our common stock.  We currently have outstanding more than 10 million warrants and options to acquire our common stock at prices between $2.50 and $9.24 per share.   We may actissue equity securities in the future for a mannernumber of reasons, including to finance our operations and business strategy, in connection with acquisitions, to adjust our ratio of debt to equity, to satisfy our obligations upon the exercise of outstanding warrants or options or for other reasons.

Additionally, we have outstanding warrants to acquire up to 285,185 shares of our common stock at an exercise price of $10.52 per share that advances its best interests and not necessarily those of other stockholders. One consequence to this substantial stockholder’s control iscontain anti-dilution adjustments that it maywill be

24


difficult for investors to remove management triggered if the sale price of the company. It could also deter unsolicited takeovers, including transactions in which stockholders might otherwise receive a premium for their shares over then current market prices.common stock is less than $10.52.


Provisions in our certificate of incorporation, bylaws, charter documents and Delaware law could discourage a change in control, or an acquisition of us by a third party, even if the acquisition would be favorable to you, thereby and adversely affect existing stockholders

Our certificate of incorporation and the Delaware General Corporation Law contain provisions that may have the effect of making more difficult or delaying attempts by others to obtain control of our company, even when these attempts may be in the best interests of stockholders. OurFor example, our certificate of incorporation also authorizes our board of directors, without stockholder approval, to issue one or more series of preferred stock, which could have voting and conversion rights that adversely affect or dilute the voting power of the holders of common stock. Delaware law also imposes conditions on certain business combination transactions with “interested stockholders.”

These provisions and others that could be adopted in the future could deter unsolicited takeovers or delay or prevent changes in our control or management, including transactions in which stockholders might otherwise receive a premium for their shares over then current market prices. These provisions may also limit the ability of stockholders to approve transactions that they may deem to be in their best interests.

We do not expect to pay dividends in the foreseeable future, and accordingly you must rely on stock appreciation for any return on your investment

We have never paid cash dividends and do not intend to do so
     We have never declared or paidno cash dividends on our common stock. Westock to date, and we currently planintend to retain our future earnings, if any, earnings to financefund the continued development and growth of our business rather thanbusiness. As a result, we do not expect to pay cash dividends. Payments of any cash dividends in the futureforeseeable future.  Further, any payment of cash dividends will also depend on our financial condition, results of operations, and capital requirements as well asand other factors, deemed relevant byincluding contractual restrictions to which we may be subject, and will be at the discretion of our board of directors.

ITEM 1B 2.UNRESOLVED STAFF COMMENTSPROPERTY
     Not applicable.
ITEM 2.PROPERTY
Information concerning our principal facilities, all of which are leased at December 31, 2006,2007, is set forth below:

Approximate
Area in
Location
 Use 
Approximate
Area in
Square Feet
11150 and 11100 Santa Monica Blvd.
Los Angeles, California
 Principal executive and administrative offices  20,000 
1315 Lincoln Blvd.
Santa Monica, California
 Medical office space for The PROMETA Center, Inc.  5,400 
1700 Montgomery St.
San Francisco, California
 Medical office space for The PROMETA Center, Inc.  4,000 

Our principal executive and administrative offices are located in Los Angeles, California and consist of leased office space totaling approximately 20,000 square feet. Our base rent is currently approximately $62,000$64,000 per month, subject to annual adjustments, with aggregate minimum lease commitments at December 31, 2006,2007, totaling approximately $3.1$2.3 million. The initial term of the lease expires in December 2010.2010, with an option to extend for five additional years.

In April 2005 we entered into a five-year lease for approximately 5,400 square feet of medical office space in Santa Monica, California, which is occupied by The PROMETA Center, Inc., which operates under a full service management agreement with us. Our base rent is currently approximately $20,000$21,000 per month. In August 2006, we entered into a five-year lease for approximately 4,000 square feet of medical office space, located in San Francisco, California, which is occupied by The PROMETA Center, Inc., at an initial base rent of approximately $11,000 per month.month, which was occupied by The PROMETA


Center, Inc., until it was closed in January 2008.  We are currently seeking to sublease this vacant space. The minimum base rent for the two medical offices are subject to annual adjustments, with aggregate minimum lease commitments at December 31, 2006,2007, totaling approximately $1.6$1.4 million.

25



In November 2006, we entered into a 5-year lease for office space in Switzerland at an initial base rent of 4,052 Swiss Francs per month (US$3,3253,600 using the December 31, 20062007 conversion rate).

In connection with a management services agreement that we executed with a treatment center in Dallas, Texas, we assumed the obligation for two lease agreements at a current combined amount of approximately $9,000 per month, which expire in May 2011.

As we expand in the future, we may lease additional regional office facilities, as necessary, to service our customer base. We believe that the current office space is adequate to meet our current needs and that additional facilities will be available for lease to meet our future needs.

ITEM 3.                  LEGAL PROCEEDINGS
     We, along with CompCare and the officers and board members
From time to time, we may be involved in litigation relating to claims arising out of CompCare, were named as defendants in two class action lawsuits filed in Delaware Chancery Court by CompCare stockholders on January 23 and February 1, 2007. The suits seek to enjoin our merger with CompCare on the grounds that it is unfair and that the directors of CompCare breached their fiduciary duties to CompCare’s minority stockholders in approving the transaction. Given their complexity and scope, and the early stageoperations in the proceedings, the final outcome and financial impactnormal course of business.  As of the litigation cannot be predicted atdate of this time. If the parties elect to terminate the merger agreement,report, we will seek toare not currently involved in any legal proceeding that we believe would have the litigation dismissed as moot.a material adverse effect on our business, financial condition or operating results.

ITEM 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS
     Not applicable.
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26



PART II

ITEM 5. MARKET FOR REGISTRANT’S COMMON EQUITY AND RELATED STOCKHOLDER MATTERS
ITEM 5.MARKET FOR REGISTRANT’S COMMON EQUITY AND RELATED STOCKHOLDER MATTERS

Our common stock is traded on The Nasdaq Global Market under the symbol “HYTM.” Prior to March 8, 2005, the stock traded on the American Stock Exchange under the symbol “HTM,” and prior to December 15, 2003 it was quoted on the Over-The-Counter Bulletin Board.
As of March 1, 2007,2008, there were approximately 10082 record holders representing approximately 4,8005,000 beneficial owners of our common stock. Following is a list by fiscal quarters of the closing sales prices of our stock:
         
  Closing Sales Prices
2006 High Low
4th Quarter $9.35  $6.20 
3rd Quarter $7.63  $4.77 
2nd Quarter $9.04  $6.52 
1st Quarter $9.19  $5.42 

         
2005 High Low
4th Quarter $6.85  $4.45 
3rd Quarter $7.30  $5.12 
2nd Quarter $8.54  $4.95 
1st Quarter $9.02  $5.24 
Dividends
  Closing Sales Prices 
2007 High  Low 
4th Quarter $8.64  $2.68 
3rd Quarter $8.77  $6.43 
2nd Quarter $8.71  $6.53 
1st Quarter $10.21  $6.48 
         
2006 High  Low 
4th Quarter $9.35  $6.20 
3rd Quarter $7.63  $4.77 
2nd Quarter $9.04  $6.52 
1st Quarter $9.19  $5.42 



Dividends

We have never declared or paid any dividends. We may, as our board of directors deems appropriate, continue to retain all earnings for use in our business or may consider paying dividends in the future.

27



COMPARISON OF 39 MONTH CUMULATIVE TOTAL RETURN*
Among
* The above graph measures the change of $100 invested in Hythiam, Inc., The common stock based on its closing price of $7.10 on September 30, 2003 and its quarter-end and December 31 year-end closing price thereafter. Hythiam, Inc.'s relative performance is then compared with the Russell 2000 Index
And Theand S & P&P Health Care Indextotal return indices.

Copyright © 2008, Standard & Poor's, a division of The McGraw-Hill Companies, Inc. All rights reserved.
www.researchdatagroup.com/S&P.htm

*The above graph measures the change of $100 invested in the Company’s stock based on its closing price of $7.10 on September 30, 2003 and its December 31 year-end closing price thereafter. The Company’s relative performance is then compared with the Russell 2000 and S & P Healthcare total return indices.
Copyright© 2007, Standard & Poor’s, a division of The McGraw-Hill Companies, Inc. All rights reserved. www.researchdatagroup.com/S&P.htm
33


Recent Sales of Unregistered Securities
     In February 2006, we issued 11,700 shares of common stock to a consultant providing investor relations services valued at $71,000. In May 2006, we issued 3,000 shares of common stock valued at $26,000 to a consultant providing website development services and 105,000 shares of common stock valued at $738,000 for the acquisition of additional intellectual property rights relating to the PROMETA protocols. In June 2006, we issued 25,000 shares of common stock valued at $171,000 to a consultant for product endorsement services. In July 2006, we issued 11,700 shares of common stock to a consultant providing investor relations services valued at $58,000. In April 2006, we issued a warrant to purchase up to 50,000 shares of common stock at an exercise price of $6.70 per share to a consultant for providing investor relations services. These securities were issued without registration pursuant to the exemption afforded by Section 4(2) of the Securities Act of 1933, as transactions by us not involving any public offering.
None

Additional information is incorporated by reference to Part III of this report.

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ITEM 6.                  SELECTED FINANCIAL DATA

The selected financial data set forth below, derived from our audited consolidated financial statements and the related notes thereto (collectively, the Financial Statements), should be read in conjunction with the Financial Statements, Item 7. Management’s Discussion and Analysis of Results of Financial Condition and Results of Operations and Item 8. Financial Statements and Supplementary Data, included elsewhere in this report.
                 
              Period from
              February 13,
              2003 to
  December 31, December
(In thousands, except per share amounts) 2006 2005 2004 31, 2003
Statement of Operations Data:
                
Revenues $3,906  $1,164  $192  $75 
Loss from operations  (39,926)  (24,872)  (11,945)  (3,545)
Net loss  (38,298)  (24,038)  (11,775)  (3,504)
                 
Loss Per Share:
                
Net loss per share — basic and diluted $(0.96) $(0.77) $(0.47) $(0.21)
Weighted average shares outstanding — basic and diluted  39,715   31,173   24,877   16,888 
                 
Cash Flows Data:
                
Net cash used in operating activities $(28,431) $(18,789) $(9,947) $(1,374)
Net cash provided by (used in) investing activities  4,662   (22,236)  (10,913)  (16,527)
Net cash provided by financing activities  26,053   40,442   21,416   21,345 

              Period from 
              February 13, 
(In thousands, except per share amounts)              2003 to 
 December 31,  December 
 2007   2006  2005  2004   31, 2003 
Statement of Operations Data:                 
Revenues:                 
Behavioral health managed care services $36,306 (a) $-  $-  $-  $- 
Healthcare services  7,695    3,906   1,164   192   75 
Total revenues  44,001    3,906   1,164   192   75 
Loss from operations  (47,531)  (d)  (39,926)  (24,872)(e)   (11,945)  (3,545)
Loss on extingishment of debt  (741)(b)                
Change in fair value of warrant liability  3,471 (c)  -   -   -   - 
Net loss  (45,462)   (38,298)  (24,038)  (11,775)  (3,504)
                     
Loss Per Share:                     
Net loss per share - basic and diluted $(0.99)  $(0.96) $(0.77) $(0.47) $(0.21)
Weighted average shares outstanding - basic and diluted  45,695    39,715   31,173   24,877   16,888 
                     
Cash Flows Data:                     
Net cash used in operating activities $(39,220)  $(28,499) $(18,819) $(9,947) $(1,374)
Net cash provided by (used in) investing activities  (4,091)   4,730   (22,206)  (10,913)  (16,527)
Net cash provided by financing activities  48,759    26,053   40,442   21,416   21,345 
                                     
 As of December 31, As of December 31, 
 2006 2005 2004 2003 2007   2006  2005  2004  2003 
Balance Sheet Data:
                      
Cash, cash equivalents and marketable securities $43,447 $47,000 $27,479 $16,640 
Cash, cash equivalents and marketable                     
securities $46,989   $43,447  $47,000  $27,479  $16,640 
Total current assets 44,549 47,720 28,093 17,344   50,342    44,549   47,720   28,093   17,344 
Total assets 52,205 54,462 33,962 22,580   70,646    52,205   54,462   33,962   22,580 
Capital lease obligations 227    
Short-term debt  4,742    -   -   -   - 
Long-term debt  2,057 (a)  -   -   -   - 
Warrant liability  2,798 (c)  -   -   -   - 
Total liabilities 10,176 4,723 2,128 2,092   27,382    10,176   4,723   2,128   2,092 
Stockholders’ equity 42,029 49,739 31,834 20,488   43,264    42,029   49,739   31,834   20,488 
Book value per share 0.96 1.27 1.07 0.83   0.80    0.96   1.27   1.07   0.83 
                     

29


(a)We began consolidating CompCare’s operations on January 13, 2007.  See further discussion in Note 5 –Acquisition of Woodcliff.
(b)The $741,000 loss on extinguishment of debt resulted from a $5 million redemption of the Highbridge senior secured notes on November 7, 2007.  See further discussion in Note 7 – Debt Outstanding.
(c)The fair value of warrants issued in conjunction with the registered direct placement on November 7, 2007 was accounted for as a liability and was revalued at $2.8 million at December 31, 2007, resulting in a $3.5 million non-operating gain.
(d)Includes a $2.4 million impairment loss related to the non-cash stock settlement reached with XINO Corporation in August 2007.  See further discussion in Note 6 – Intangible Assets.
(e)We recorded an impairment charge of $272,000 in December 2005 to fully write off the cost of a patent for opiate addiction treatment.  See further discussion in Note 6 – Intangible Assets.


ITEM 7. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
ITEM 7.MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
Forward-Looking
Forward-Looking Statements

The forward-looking comments contained in the following discussion involve risks and uncertainties. Our actual results may differ materially from those discussed here due to factors such as, among others, limited operating history, difficulty in developing, exploiting and protecting proprietary technologies, intense competition and substantial regulation in the healthcare industry. Additional factors that could cause or contribute to such differences can be found in the following discussion, as well as under Item 1A, “Risks Factors.”
Overview
OVERVIEW

General

We are a healthcare services management company, focused on delivering solutions for those suffering from alcoholismproviding behavioral health management services to health plans, employers, criminal justice, and other substance dependencies.government agencies through a network of licensed and company managed healthcare providers. We also research, develop, license and commercialize innovative physiological, nutritional, and behavioral treatment protocols.programs. We manage behavioral health disorders through our majority-owned subsidiary, Comprehensive Care Corporation (CompCare). We utilize CompCare’s infrastructure to offer our proprietary disease management programs forservices. Our disease management offering combines medical and behavioral treatment modalities to manage substance dependencedependent populations, and is built around our proprietary PROMETA® treatment protocolsPROMETA® Treatment Programs for alcoholism and dependence to stimulants.cocaine and methamphetamines. Our PROMETA Treatment with our PROMETA protocols, whichPrograms--which integrate behavioral, nutritional, and medical components, arecomponents--are available through physicians and other licensed treatment providers who have entered into licensing agreements with us for the use of our protocols.programs. We also license or manage treatment centers that offer the PROMETA Centers, medical practicesTreatment Programs, as well as other treatments for substance dependencies.

Our Strategy

Our business strategy is to provide quality treatment programs that will become the standard-of-care for those suffering from alcoholism and other substance dependencies in a cost effective manner. We intend to focus on offeringdisease management and managed care and grow our business through increased adoption of our PROMETA Treatment Programs and a substance abuse disease management treatment with the PROMETA protocolsapproach for dependencies on alcohol, cocainemanaged care, self-insured employers, unions, government agencies, criminal justice systems, and methamphetamines.other third-party payers, in addition to increased utilization from within existing and new licensees and managed treatment centers for substance dependencies.
Our Strategy
Key elements of our business strategy include:

Expanding the base of our licensed treatment sites, focusing on existing service areas
Increasing the number of dedicated PROMETA Centers in major U.S. markets
Demonstrating the potential for improved clinical outcomes and cost effectiveness associated with the use of PROMETA treatment protocols through commercial pilot studies with key managed care and other third-party payers
Leveraging existing and initiating new pilot studies with governmental agencies to accelerate the adoption and funding by criminal justice, state and local government systems
·      Providing our substance abuse disease management program to managed care health plans for reimbursement on a case rate or capitated basis, utilizing the CompCare infrastructure to provide basicsome service components

·      Demonstrating the potential for improved clinical outcomes and cost effectiveness associated with using the PROMETA Treatment Programs, through commercial pilot studies with key managed care servicesand other third-party payers

·      Expanding the base of our self-pay licensed treatment sites and managed medical treatment centers, focusing primarily on existing service areas

·      Seeking additional scientific and clinical research data to further validate the efficacy of using the PROMETA protocolsTreatment Programs through unrestricted grants for research studies by leading research institutions and preeminent researchers in the field of alcohol and substance abuse


·      Exploring opportunities in foreign markets where our PROMETA patents have been issued.
Operations
CompCare Acquisition

Effective January 12, 2007, we acquired a 50.25% controlling interest in CompCare through the acquisition of Woodcliff Healthcare Investment Partners, LLP (Woodcliff). Our consolidated financial statements include the business and operations of CompCare subsequent to this date.

CompCare provides managed care services in the behavioral health and psychiatric fields.  CompCare manages the delivery of a continuum of psychiatric and substance abuse services to commercial, Medicare and Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators, and commercial and other group purchasers of behavioral healthcare services.  The customer base for CompCare’s services includes both private and governmental entities.

Segment Reporting

We currently operate within two reportable segments: healthcare services and behavioral health managed care services. Our healthcare services segment focuses on providing licensing, administrative and management services to licensees that administer PROMETA and other treatment programs, including managed treatment centers that are licensed and/or managed by us. Our behavioral health managed care services segment focuses on providing managed care services in the behavioral health, psychiatric and substance abuse fields, and principally includes the operations of our majority-owned, controlled subsidiary, CompCare. A majority of our consolidated revenues and assets are earned or located within the United States.

Operations

Healthcare Services

Under our licensing agreements, we provide physicians and other licensed treatment providers access to our PROMETA protocols,Treatment Programs, education and training in the implementation and use of the licensed technology and marketing support. The patient’s physician determines the appropriateness of the use of the PROMETA Treatment Program. We receive a fee for the licensed technology and related services generally on a per patient basis. At the end of 2004, we had seven licensed sites, of which one licensee had generated 93% of our revenues that year.  In 2005 and 2006, throughThrough increased efforts to obtain additional licensing agreements with hospitals and healthcare providers in major U.S. markets, we added an additionalincreased the number of sites by 25, 29 and 2940 sites in 2005, 2006 and 2007, respectively, bringing the total number of licensed sites throughout the United States to 61101 as of December 31, 2006,2007, with 4170 sites contributing to revenues in 2006.2007.

30



Managed Medical Practices and Treatment Centers

     We believe that the number of patients treated by our licensees will increase over time as we launch a new nationwide team of field personnel in early 2007 to increase the awareness and benefits of PROMETA among physicians and other healthcare professionals specializing in the treatment of substance dependence, and clinical outcomes data from research studies become available.
PROMETA Centers
    In December 2005, David E. Smith,The PROMETA Center, Inc., a medical professional corporation (now owned by Lawrence Weinstein, M.D., a renowned addiction medicine specialist and founderour senior vice president of the Haight Ashbury Free Clinics,medical affairs), opened the PROMETA Center, a new medical practice operating in a state-of-the-art outpatient facility located in Santa Monica, California, that we built out under a lease agreement. Under the terms of a full business service management agreement with Dr. Smith’s professional corporation, The PROMETA Center, Inc., we manage the business components of the medical practice and license the PROMETA protocolsTreatment Programs and use of the name in exchange for management and licensing fees. The practice has a focus on offeringoffers treatment with the PROMETA protocolsTreatment Programs for dependencies on alcohol, cocaine and methamphetamines, but also offers medical interventions for other substance dependencies. The financial results of The PROMETA Center, Inc. are included in our consolidated financial statements under accounting standards applicable to variable interest entities. Revenues from the PROMETA Center accounted for approximately 29% of our consolidated revenues in 2006.

In January 2007, Dr. Smith opened a second PROMETA Center was opened in San Francisco, California,which was subsequently closed in January 2008.

In 2007 we entered into additional management services agreements with other medical corporations and treatment centers, under similar terms and conditions, including the terms of our management agreement with The PROMETAMurray Hill Recovery Center Inc.located in Dallas, Texas. In addition,


we have entered into a licensing and administrative services agreement with Canterbury Institute, LLC, (Canterbury), which manages a newly openedtwo PROMETA Center medical practiceteatment centers in New Jersey and Florida.

Revenues from licensed and managed treatment centers, including the PROMETA Centers, accounted for approximately 31% of our healthcare services revenues in January 2007, and plans to manage a second center to be opened in Southern Florida in the second quarter 2007. As part of the agreement, we will receive a 10% share of Canterbury’s profits in each Canterbury licensed center, in addition to fees for licensing and administrative services.

Research and Development, Pilot Studies
     In
To date, we have spent approximately $9.2 million related to research and development, including $3.3 million in 2007, $3.1 million in 2006 and $2.6 million in 2005, respectively, in funding for commercial pilots and 2006 we funded through unrestricted grants for a number of clinical research studies by preeminent researchers in the field of substance dependence and leading research institutions to evaluate the efficacy of the PROMETA Treatment Program in treating alcohol and stimulant dependence.  In addition, pilotWe plan to spend approximately $4.9 million in 2008 for unrestricted research grants and commercial pilots.

Pilot programs are used in conjunction with drug court systems, state programs and managed care organizations were commenced by those entitiesto allow such programs to evaluate the outcomes and cost effectiveness of treatment with the PROMETA protocols. Successful results to date from severalTreatment Programs. The focus of these research studiespilot programs is to assist such organizations in assessing the impact on their population, and pilots that have been completed have provided formal third-party validation of PROMETA. Asas a result, of two of thesethe method, manner, timing, participants and metrics may change and develop over time, based on initial results from the particular program, other pilots, the Pierce County Allianceand research studies. We generally do not provide updates on status after a pilot is initially announced.

International

We have expanded our operations in the State of Washington and the City Court of Gary, Indiana have adopted the PROMETA protocols in their respective drug court systems, which we view as important milestones and as references for our efforts in the criminal justice system.
     We anticipate that the research studies, including studies to be completed throughout 2007 and 2008, will be the basis for publication in scientific journals, and key to our success in validating the efficacy of PROMETA as the preferred method of care for treating alcoholism and stimulant dependence and serve to accelerate our growth. To date, we have spent approximately $6 million related to research and development ($3.1 million, $2.6 million and $177,000 in 2006, 2005 and 2004, respectively) and plan to spend and additional $6.7 million in 2007 and 2008 for unrestricted research grants and commercial pilots.
CompCare Acquisition
     Effective January 12, 2007, we acquired a 50.2% controlling interest in Comprehensive Care Corporation (CompCare) through the acquisition of Woodcliff Healthcare Investment Partners, LLP. EffectiveEurope, with our acquisition of Woodcliff, our consolidated financial statements will include the business and operations of CompCare. On January 18, 2007, we entered into an Agreement and Plan of Merger, and on January 26, 2007 we entered into an amended and restated Agreement and Plan of Merger, with CompCare, pursuant to which we would acquire the remaining outstanding shares of CompCare. Litigation to enjoin the merger is currently pending, and it is unclear at this time whether the merger will proceed or if the merger agreement will be terminated by the parties.
     CompCare provides managed care services in the behavioral health and psychiatric fields. CompCare manages the delivery of a continuum of psychiatric and substance abuse services to commercial, Medicare and

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Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators, and commercial and other group purchasers of behavioral healthcare services. The customer base for CompCare’s services includes both private and governmental entities.
International
     In 2006, our Swiss foreign subsidiary signedsigning PROMETA license and services agreements with three sites in Switzerland in 2006 to serve the international market.  TheThese sites in Switzerland have commenced operations in the first quarter of 2007.  Our other internationalEuropean operations were also expanded in 2007 to date have not yet been significant, consisting primarily ofinclude the treatment of dependenciesother dependencies.  In August 2007 we signed a PROMETA licensing agreement with a leading hospital in Panama, which commenced operations in September 2007.

Recent Developments

In January 2008, we streamlined our operations to increase our focus on disease management and managed care opportunities, which is expected to result in an overall reduction of 25% to 30% of cash operating expenses for the year ending December 31, 2008 from 2007 levels. The actions we took included eliminating field and regional sales personnel and related corporate support personnel, closing the PROMETA Center in San Francisco,  a reduction in outside consultants and overall reductions in overhead costs.  Estimated one-time costs associated with these actions were approximately $1.0 million and will be recognized as a charge to operating expenses in the statement of operations for the quarter ending March 31, 2008. Such costs primarily represent severance payments and related benefits and costs incurred in closing the San Francisco PROMETA Center. We do not expect to incur any material additional costs associated with this initiative. We also anticipate that in addition to previously entered into and announced business relationships, new disease management agreements from labor unions, self-insured employers, and managed care health plans will add to the current self-pay revenue base and result in increased revenues for 2008. The combination of increased revenues and cost reductions is expected to reduce the company's net cash utilization for 2008 compared to 2007. Following the streamlining actions taken in January 2008, we anticipate that our cash operating expenditures will average approximately $2.5 million per month for the remainder of 2008 compared to an average of approximately $3.6 million per month in the fourth quarter 2007,  excluding research and development costs and costs incurred by our consolidated subsidiary, CompCare. We believe that existing capital resources will be sufficient to fund our operating expenses and capital requirements until we achieve positive cash flow, which we believe will be within the next two years.

On November 1, 2007, we announced the top line results of an 88-patient randomized, double-blind, placebo-controlled study conducted by Harold Urschel, M.D. The 30-day study on cravings and neurocognition funded by us was a follow-up to Dr. Urschel’s 90-day open-label study on the effects of the PROMETA Treatment Program in treatment-seeking, methamphetamine-dependent subjects. The resulting data showed a statistically significant reduction in cravings versus placebo.


These placebo-controlled outcomes confirmed the findings in a prior study by Dr. Urschel, which showed that there was an immediate reduction of cravings within the one-month treatment period.  Dr. Urschel’s prior study was published in Mayo Clinic Proceedings, a peer-reviewed medical journal, in their October 2007 installment and was an open-label study of the pharmacological component of the PROMETA Treatment Program for methamphetamine dependence. According to the publication, over 80% of the study's 50 participants experienced a statistically significant reduction in cravings for methamphetamine with no adverse events from the treatment.
On November 7, 2007, we entered into securities purchase agreements with select institutional investors in a registered direct placement, in which we issued an aggregate of approximately 9.6 million shares of common stock at a price of $4.79 per share, for gross proceeds of approximately $46.2 million before related fees and offering expenses. We also issued 5-year warrants to purchase an aggregate of approximately 2.4 million additional shares of our common stock at an exercise price of $5.75 per share.  The fair value of the warrants at the date of issue amounted to approximately $6.3 million and was accounted for as a liability in accordance with the Financial Accounting Standards Board (FASB) Emerging Issues Task Force Issue No. 00-19, "Accounting for Derivative Financial Instruments Indexed to, and Potentially Settled in, a Company's Own Stock" (EITF 00-19). The shares and warrants were sold pursuant to our shelf registration statement on Form S-3 filed with the SEC on September 6, 2007 and declared effective on October 5, 2007. We intend to use the proceeds of the registered direct common stock placement for working capital and general corporate purposes.

Included in the gross proceeds was $5.35 million from the conversion of $5 million of the senior secured notes issued to Highbridge, which includes $350,000 based on a pilotredemption price of 107% of the principal amount being redeemed pursuant to a redemption agreement entered into with Highbridge on November 7, 2007. The $350,000 was included as part of the reacquisition cost of the notes and the difference between the reacquisition price and the net carrying amount of the principal amount being redeemed amounted to $741,000 and was recognized as a loss on extinguishment of debt in our statement of operations during the fourth quarter of 2007.

Behavioral Health Managed Care Services

Our consolidated subsidiary, CompCare, typically enters into contracts on an annual basis legalto provide managed behavioral healthcare and substance abuse treatment to clients’ members. Arrangements with clients fall into two broad categories: capitation arrangements, where clients pay CompCare a fixed fee per member per month, and fee-for-service and administrative service arrangements where CompCare may manage behavioral healthcare programs or perform various managed care services. Approximately $35.2 million, or 97% of CompCare’s revenues for the period January 13 through December 31, 2007, were derived from capitation arrangements. Under capitation arrangements, CompCare receives premiums from clients based on the number of covered members as reported by the clients. CompCare reviews membership eligibility records and other developmentreported information to verify its accuracy in determining the amount of revenue to be recognized. The amount of premiums received for each member is fixed at the beginning of the contract term. These premiums may be subsequently adjusted, up or down, generally at the commencement of each renewal period.



Effective January 1, 2007, CompCare commenced a contract with a health plan to provide behavioral healthcare services to approximately 250,000 Medicaid recipients in Indiana. This contract amounted to $14.6 million in revenues for the period January 13 through December 31, 2007, and start up activities. We will continueis anticipated to evaluategenerate approximately $16 million to $17 million in annual revenues in 2008.

Seasonality of Business

Historically, CompCare’s managed care plans have experienced increased member utilization during the successmonths of March, April and May, and consistently lower utilization by members during the months of June, July, and August.  Such variations in member utilization impact the costs of care during these months, generally having a negative impact on gross margins and operating profits during the former period, and a positive impact on gross margins and operating profits during the latter period.
Concentration of Risk

For the period January 13 through December 31, 2007, 87% of behavioral health managed care services revenue (or 72% of our consolidated revenues for the year ended December 31, 2007) was concentrated in contracts with six health plans to provide behavioral healthcare services under commercial, Medicare, Medicaid, and children’s health insurance plans (CHIP).  This includes the new Indiana Medicaid HMO contract, which represented approximately 40% of behavioral health managed care services revenue for the period January 13 through December 31, 2007 (or 33% of our consolidated revenues for the year ended December 31, 2007). The term of each contract is generally for one year and is automatically renewable for additional one-year periods unless terminated by either party by giving the requisite written notice.  The loss of one or more of these initial programs before we pursue additional international expansion.clients, unless replaced by new business, would have an adverse impact on the financial condition of CompCare.
Segment Reporting
     We currently operateRecent Developments

On January 4, 2008 CompCare announced the appointment of John M. Hill as its new President and Chief Executive Officer, replacing Mary Jane Johnson, who resigned for health reasons effective December 14, 2007.

In January 2008, CompCare’s Pennsylvania and Maryland Medicare Advantage health plan client, representing $5.4 million, or 15%, of CompCare’s total revenue during 2007, issued a request for proposal (RFP) for management of behavioral healthcare services for its Pennsylvania, Maryland and Texas regions. CompCare submitted a bid to retain its current business from this client as well as attempt to contract for the Texas membership. This client intends to select a finalist in one reportable segment focused onMarch 2008 with an effective date of July 1, 2008 for a new agreement. CompCare does not expect to be selected as a finalist and accordingly the majority of the revenues under this contract are expected to end during the third quarter of 2008.

One of CompCare’s existing commercial health plan clients in Indiana has decided to exit the group health plan business. Beginning January 1, 2008 and throughout the remainder of 2008, this health plan will not be renewing any of its existing customer contracts, as all of their members are being transitioned to other health plans.  This health plan accounted for approximately 5.0% of behavioral health managed care services revenues for the period January 13 through December 31, 2007.

On August 1, 2007, CompCare began providing licensing, administrative and managementbehavioral healthcare services to licensees that administer PROMETAapproximately 23,000 Medicare members of an existing client in Pennsylvania.  Such services are estimated to generate between $4.5 and other treatment protocols, including PROMETA Centers that are licensed and/or managed by us. Substantially all$5.0 million in annual revenues.

On July 19, 2007, CompCare received from an existing client in Texas a notice of our licensing and service-related revenues and assets are earned or located withintermination, which resulted in termination of the United States.
     Beginning on January 12, 2007, our consolidated results will include the operationscontract effective November 30, 2007.  This client accounted for approximately 8% of CompCare, which will be presented in a separate reportable segment focused on providingbehavioral health managed care services.services revenues for the period January 13 through December 31, 2007 and had been a customer since 1998.

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ResultsCompCare has entered into negotiations with its major Indiana HMO client to obtain a rate increase to offset higher than expected costs of Operationsutilization.  CompCare believes it will receive a rate increase effective January 1, 2008, provided it complies with monthly performance measures it believes it will meet. The rate increase would amount to approximately $2.0 million per annum.


     The table below and the discussion that follows summarize our results of operations and certain selected operating statistics for the last three fiscal years (amounts in thousands except patient treatment data):
             
  Year Ended December 31, 
(In thousands) 2006  2005  2004 
Revenues
            
U.S. licensees $2,650  $1,105  $192 
PROMETA Center  1,137   59    
Other revenues  119       
          
Total revenues
  3,906   1,164   192 
Operating expenses
            
Cost of services  818   134   17 
General and administrative expenses            
Salaries and benefits  16,212   9,204   5,117 
Other expenses  22,468   13,173   6,156 
Research and development  3,053   2,646   177 
Depreciation and amortization  1,281   879   670 
          
Total operating expenses  43,832   26,036   12,137 
          
Loss from operations
  (39,926)  (24,872)  (11,945)
Interest income  1,630   834   171 
          
Loss before provision for income taxes
 $(38,296) $(24,038) $(11,774)
          
Patients treated
            
U.S. licensees  427   207   40 
PROMETA Center  140   9    
Average revenue per patient treated
            
U.S. licensees $6,206  $5,337  $4,800 
PROMETA Center  8,121   6,564    
How We Measure Our Results
Year Ended December 31, 2006 Compared to Year Ended December 31, 2005
Revenues
Our healthcare services revenues are generated from fees that we charge to hospitals, healthcare facilities and other healthcare providers that license our PROMETA protocols,Treatment Programs, and from patient service revenues related to our licensing and management services agreementagreements with the PROMETA Center.managed treatment centers. Our technology license and management services agreements provide for an initial fee for training and other start-up related costs, plus a combined fee for the licensed technology and other related administrative services, generally set on a per-treatment basis, and thus a substantial portion of our revenues areis closely related to the number of patients treated. Patients treated by the PROMETA Centermanaged treatment centers generate higher average revenues per PROMETA patient than our other licensed sites due to consolidation of itstheir gross patient revenues in our financial statements.  Key indicators of our financial performance are the number of facilities and healthcare providers that contract with us to license our technology and the number of patients that are treated by those providers using the PROMETA protocols.Treatment Programs. Additionally, our financial results will depend on our ability to expand the adoption of PROMETA among government and other third party payer groups, and our ability to effectively price these products, and manage general, administrative and other operating costs.

For behavioral health managed care services, our largest expense is CompCare’s cost of behavioral health managed care services that it provides, which is based primarily on its arrangements with healthcare providers. Since CompCare’s costs are subject to increases in healthcare operating expenses based on an increase in the number and frequency of the members seeking behavioral health care services, CompCare’s profitability depends on its ability to predict and effectively manage healthcare operating expenses in relation to the fixed premiums it receives under capitation arrangements.  Providing services on a capitation basis exposes CompCare to the risk that its contracts may ultimately be unprofitable if CompCare is unable to anticipate or control healthcare costs.   Estimation of healthcare operating expense is one of our most significant critical accounting estimates. See “Management’s Discussion and Analysis of Financial Condition and Results of Operations — Critical Accounting Estimates.”

CompCare currently depends upon a relatively small number of customers for a significant percentage of its behavioral health managed care operating revenues. A significant reduction in sales to any of CompCare’s large customers or a customer exerting significant pricing and margin pressures on CompCare would have a material adverse effect on our consolidated results of operations and financial condition. In the past, some of CompCare’s customers have terminated their arrangements or have significantly reduced the amount of services requested. There can be no assurance that present or future customers will not terminate their arrangements or significantly reduce the amount of services requested. Any such termination of a relationship or reduction in use of CompCare's services would have a material adverse effect on our consolidated results of operations or financial condition (see Note 13 — Major Customers/Contracts).



Results of Operations

Table of Summary Financial Information

The table below and the discussion that follows summarize our results of operations and certain selected operating statistics for the last three fiscal years (amounts in thousands except patient treatment data):
          
(In thousands) Year Ended December 31, 2007 
  2007  2006  2005 
Revenues         
Behavioral health managed care services $36,306  $-  $- 
Healthcare services  7,695   3,906   1,164 
Total revenues  44,001   3,906   1,164 
Operating Expenses            
Behavioral health managed care expenses  35,679   -   - 
Cost of healthcare services  2,052   818   134 
General and administrative expenses  45,554   38,680   22,105 
Impairment loss  2,387   -   272 
Research and development  3,358   3,053   2,646 
Depreciation and amortization  2,502   1,281   879 
Total operating expenses  91,532   43,832   26,036 
Loss from operations  (47,531)  (39,926)  (24,872)
Interest income  1,584   1,630   834 
Interest expense  (2,190)  -   - 
Loss on extinguishment of debt  (741)  -   - 
Change in fair value of warrant liability  3,471   -   - 
Other non-operating expense, net  32   -   - 
Loss before provision for income taxes $(45,375) $(38,296) $(24,038)

Summary of Consolidated Operating Results

We acquired a majority controlling interest in CompCare, resulting from our acquisition of Woodcliff on January 12, 2007, and began including its results in our consolidated financial statements subsequent to that date. These results are reported in our behavioral health managed care services segment.
 In
The increased loss in 2007 compared to 2006 is due to the inclusion of a loss of $4.1 million from CompCare, including purchase accounting adjustments, higher operating expenses, $2.4 million impairment loss, and $741 thousand loss on extinguishment of debt, partially offset by an increase in revenues from our healthcare services segment and the $3.5 million fair value adjustment of the warrant liability.
The increase in the loss before provision for income taxes in 2006 compared to 2005 was due to significantly higher operating costs as we expanded our business operations.

Our healthcare services revenues nearly doubled in 2007 when compared to 2006. The increase was due to the increase in the number of patients treated at our U.S. licensed sites and at our managed treatment centers, administrative fees from new licensees and other revenues from the commencement of international operations and licenses with government agencies and other third-party payers.

The increase in revenues between 2006 and 2005 was primarily attributable to the increase in the number of patients treated at our U.S. license sites and at the managed treatment centers.



Excluding the impact of CompCare, total operating expenses for the year ended December 31, 2007 increased by approximately $7.4 million when compared to the same period in 2006. The increase is due mainly to the $2.4 million impairment loss related to the non-cash stock settlement reached with XINO Corporation (as discussed more fully in “Healthcare Services” below), the increase in the number of our sales field personnel, the expansion in number of licensees, the strengthening and expansion in our management and support teams, the funding of clinical research studies and investment in development of additional markets for our services, including managed care, statewide agencies, criminal justice systems and other third-party payers as well as international opportunities.

Total share based compensation expense decreased to $2.6 million for the year ended December 31, 2007 compared to $3.7 for the same period in 2006 due principally to the decline in market value of our common stock.  The 2006 expense increased from the $1.7 million incurred in 2005 due to the adoption of SFAS No.123R, “Share-based Payment” (SFAS 123R).

We incurred approximately $1.9 million of interest expense during the year ended December 31, 2007 associated with the CompCare acquisition-related financing with Highbridge that originally consisted of the issuance of a $10 million senior secured note and warrants to purchase up to approximately 250,000 shares of our common stock.

Reconciliation of Segment Results

The following table summarizes and reconciles the loss from operations of our reportable segments to the loss before provision for income taxes from our consolidated statements of operations for the years ended December 31, 2007, 2006 and 2005:

  Year Ended December 31, 
(In thousands) 2007  2006  2005 
          
Healthcare services $(41,270) $(38,296) $(24,038)
Behavioral health managed care services  (4,105)  -   - 
Loss before provision for income taxes $(45,375) $(38,296) $(24,038)
             



Healthcare Services

The following table summarizes the operating results for healthcare services for the years ended December 31, 2007, 2006 and 2005:

(In thousands, except patient treatment data) December 31, 
  2007  2006  2005 
Revenues         
U.S. licensees $3,807  $2,650  $1,105 
Managed treatment centers (a)  2,416   1,137   59 
Other revenues  1,472   119   - 
Total revenues  7,695   3,906   1,164 
Operating Expenses            
Cost of healthcare services  2,052   818   134 
General and administrative expenses            
Salaries and benefits  21,272   16,212   9,204 
Other expenses  20,561   22,468   12,901 
Impairment loss  2,387   -   272 
Research and development  3,358   3,053   2,646 
Depreciation and amortization  1,578   1,281   879 
Total operating expenses  51,208   43,832   26,036 
Loss from operations  (43,513)  (39,926)  (24,872)
Interest income  1,439   1,630   834 
Interest expense  (1,926)  -   - 
Loss on extinguishment of debt  (741)  -   - 
Change in fair value of warrant liability  3,471   -   - 
Loss before provision for income taxes $(41,270) $(38,296) $(24,038)
             
PROMETA Patients Treated            
U.S. licensees  559   427   207 
Managed treatment centers (a)  239   140   9 
Other  124   15   - 
   922   582   216 
Average revenue per PROMETA patient treated  (b)            
U.S. licensees $5,444  $5,915  $5,337 
Managed treatment centers (a)  8,840   8,121   6,564 
Other  5,810   2,463   - 
Overall average  6,374   6,357   5,388 

(a) Includes managed and/or licensed PROMETA Centers.
(b) The average revenue per patient treated excludes administrative fees and other non-PROMETA patient revenues.

Year Ended December 31, 2007 Compared to Year Ended December 31, 2006

Revenues

Revenues for the year ended December 31, 2007 nearly doubled compared to 2006, due to an increase in the number of patients treated across all of our markets, expansion of the number of contributing licensees, administrative fees from new licensees and other revenues from the commencement of international operations and licenses with third-party payers. The number of PROMETA patients treated increased by 58% in 2007 compared to 2006. The number of licensed sites that contributed to revenues increased to 70 for the year ended December 31, 2007 compared to 41 sites contributing to revenues in 2006, including two new PROMETA Centers that were


opened in San Francisco and New Jersey in January 2007, and the addition of a managed treatment center in Dallas, Texas, in August 2007.  The average revenue per patient treated at U.S. licensed sites in 2007 decreased compared to 2006 due to higher average discounts granted by our licensees resulting principally from the launch of a patient assistance program with our licensees, new site training and business development initiatives. The average revenue for PROMETA patients treated at the managed treatment centers increased in 2007 from 2006 due to a lower percentage of discounted and training patients, and is higher than our other licensed sites due to the consolidation of their gross patient revenues in our financial statements. Other revenues in 2007 consisted of revenues from our international operations and third-party payers. International revenues in 2007 include the commencement of operations in Europe in the first quarter of 2007 and revenues from Panama commencing in September 2007.

Operating Expenses

Total operating expenses increased by $7.4 million during the year ended December 31, 2007 compared to the same period in 2006, as we incurred a $2.4 million impairment loss related to the non-cash stock settlement reached with XINO Corporation, increased the number of U.S.our sales field personnel, expanded the number of licensees, strengthened and expanded our management and support teams, funded clinical research studies and invested in development of additional markets for our services, including managed care, statewide agencies, criminal justice systems and other third-party payers as well as international opportunities.

Cost of healthcare services consists of royalties we pay for the use of the PROMETA Treatment Program, and costs incurred by our consolidated managed treatment centers (including PROMETA Centers) for direct labor costs for physicians and nursing staff, continuing care expense, medical supplies and treatment program medicine costs. The increase in these costs primarily reflects the increase in revenues from these treatment centers, including the new sites added in 2007 discussed above.

General and administrative expenses consist primarily of salaries and benefits expense and other operating expense, including support and occupancy costs, outside services and marketing. General and administrative expenses increased by $3.2 million during the year ended December 31, 2007 compared to the same period in 2006, due mainly to an increase in salaries and benefits expenses and support and occupancy costs, partially offset by reductions in certain outside services costs and advertising expenses. Salaries and benefits expenses increased by $5.1 million in 2007 compared to 2006, due to the increase in personnel from 120 employees at December 31, 2006 to approximately 160 employees at December 31, 2007, as we added managers and staff in the field to support our licensed sites, increased our corporate staff to support our rapid growth in operations, research, sales and marketing efforts, new business initiatives and general and administrative functions. Support and occupancy costs, such as insurance, rent and travel costs, increased by $2.5 million in 2007 compared to 2006 due to the growth of our business and the resulting overall increase in staffing and corporate infrastructure to support this growth.  Costs related to outside services, such as audit, legal, investor relations, marketing, business development and other consulting expenses and non-cash stock-based compensation charges for services received from 32non-employees, decreased by $1.9 million in 2007 compared to 612006. Advertising expense declined to $872,000 from $3.4 million in 2006, primarily due to increased costs for a drug addiction awareness campaign for PROMETA in the first half of 2006.

The impairment loss of $2.4 million resulted from the non-cash settlement agreement reached with XINO Corporation in August 2007 to release 310,000 of the 360,000 shares of our common stock previously issued to XINO in 2003 in connection with our acquisition of a patent for a treatment method for opiate addition, which has never been utilized in our business plan.

Research and development expense increased by $306,000 in 2007 compared to 2006 due to an increase in funding for unrestricted grants for research studies to evaluate the clinical effectiveness of our PROMETA Treatment Programs and the commencement of additional commercial pilot studies. We plan to spend $4.9 million in 2008 for such studies.

In January 2008, we streamlined our operations to increase our focus on disease management and managed care opportunities, which is expected to result in an overall reduction of 25% to 30% of cash operating expenses for the year ending December 31, 2008. See Healthcare Services - Recent Developments above.


Interest Income

Interest income for the year ended December 31, 2007 decreased compared to the same period in 2006 due to a decrease in the average invested balance of cash equivalents and marketable securities, and a decrease in average interest rates.

Interest Expense

Interest expense primarily relates to the $10 million senior secured note issued on January 17, 2007 to finance the CompCare acquisition, accrued at year-end. a rate equal to prime plus 2.5% (9.75% at December 31, 2007). For the year ended December 31, 2007, interest expense includes $949,000 in amortization of the $1.4 million discount resulting from the value allocated to the warrants issued with the debt and related borrowing costs.  As discussed more fully in Note 7 – Debt Outstanding, we entered into a redemption agreement to redeem $5 million in principal related to the senior secured notes as part of the securities offering completed on November 7, 2007.

Loss on extinguishment of debt

The PROMETA Centerloss on extinguishment of debt of $741,000 was due to a redemption agreement with Highbridge to redeem $5 million in Southern California,principal related to the senior secured notes as part of our securities offering completed on November 7, 2007. The loss represents the difference between the reacquisition price, which openedincluded $350,000 for an early redemption penalty, and the net carrying amount of the principal amount being redeemed and related deferred costs of issuance.

Change in December 2005,fair value of warrant liability

We issued 5-year warrants to purchase an aggregate of approximately 2.4 million additional shares of our common stock at an exercise price of $5.75 per share in connection with a registered direct stock placement completed on November 7, 2007. The proceeds attributable to the warrants, based on the fair value of the warrants at the date of issue, amounted to approximately $6.3 million, and is accounted for approximately 29%as a liability in accordance with EITF 00-19. The warrant liability was revalued at $2.8 million at December 31, 2007, resulting in a $3.5 million non-operating gain to the statement of our revenues in 2006. No other licensee accounted for over 10% of our revenues last year, whereas inoperations. We will continue to mark the warrants to market value each quarter-end until they are completely settled.

Year Ended December 31, 2006 Compared to Year Ended December 31, 2005 three of our licensees each

33


accounted for over 10% of our revenues, representing 25%, 20% and 18% of our revenues. Three licensees accounted for 63% of our revenues in 2005 and one licensee accounted for 93% of our revenues in 2004. Other revenues in 2006 consisted of revenues from third-party payers and start-up international operations.

Revenues

 Revenues for the years ended December 31, 2006 and 2005 were $3.9 million and $1.2 million, respectively, an increase of 236%.  The increase in revenues was primarily attributable to the increase in the number of patients treated at our U.S. licensed sites and at the PROMETA Center.  In addition, our average license fees per patient treatment at U.S licensed sites increased by 17% from $5,337 in 2005 to $6,206$5,915 in 2006, primarily due to lower average discounts granted by our licensees in the current year2006 than in the same period last year.2005. There were no significant changes in our licensing fees charged to our licensees between the periods. The average revenue for patients treated at the PROMETA Center in 2006 was $8,121, which is higher than our other licensed sites due to the consolidation of its gross patient revenues in our financial statements.

Operating Expenses

Our operating expenses increased from $26.0 million in 2005 to $43.8 million in 2006, as we expanded the number of licensees, strengthened and expanded our management and support teams, increased brand awareness, marketing and advertising for our PROMETA protocols,Treatment Programs, funded clinical research studies and invested in development of additional markets for our services, including managed care, statewide agencies, criminal justice systems and other third-party payers as well as international opportunities.

Cost of services consists of royalties we pay for the use of the PROMETA treatment protocol,Treatment Program, and the PROMETA Center’s direct labor costs for its physician and nursing staff, continuing care expense, medical supplies


and protocolprogram medicine costs for patients treated at the PROMETA Center. The increase in these costs primarily reflects a full year of operation at the PROMETA Center, which opened in December 2005, and the related increase in revenues.

Salaries and benefits expenses were $16.2 million and $9.2 million for the years ended December 31, 2006 and 2005, respectively.  The significant increases in 2006 over 2005 reflect the increase in personnel from 90 to approximately 120 employees at the end of 2006, as we have added managers in the field to support our licensed sites and have increased our corporate staff to support our rapid growth in operations, research, sales and marketing efforts, new business initiatives and general and administrative functions.  Additionally, the increase in 2006 includes $2.3 million of non-cash expense for stock options granted to employees and directors, resulting from our adoption of Statement of Financial Accounting Standards (SFAS) No.SFAS 123R “Share-based Expense” (SFAS 123R), on January 1, 2006. In 2005 and prior years such costs were not included in our statements of operations, but were reflected as pro forma disclosures in the footnotes to the financial statements.

Other expenses amounted to $22.5 million and $13.2$12.9 million for the years ended December 31, 2006 and 2005, respectively, which included non-cash charges of $1.4 million and $1.7 million, respectively, related to the issuance of common stock, stock options and warrants for services received from non employees.  Other expenses include advertising, legal, audit, insurance, rent, travel and entertainment, investor relations, marketing, business development and other professional consulting costs.  Most expenditures increased significantly in 2006 from 2005, due to the rapid growth of our business and the resulting overall increase in staffing and corporate infrastructure to support this growth.  Additionally, in 2006, we increased spending in marketing and direct-to-consumer advertising in some of the major metropolitan services areas, where we have established a market presence.  Our advertising costs increased from $1.1 million in 2005 to $3.3 million in 2006, a significant portion of which was spent on a branding awareness campaign for PROMETA. We also incurred higher costs for auditing and consulting costs for Sarbanes-Oxley Section 404 compliance and new initiatives for expanding our business to managed care, statewide agencies, government affairs, the gay community and international developmental activities.

In 2006 we incurred approximately $3.1 million for research and development, compared to $2.6 million in 2005, as we funded unrestricted grants for research studies to evaluate the clinical effectiveness of our PROMETA protocolsTreatment Programs and commenced additional commercial pilot studies.  We plan to spend approximately $6.7 million over the next two years for such studies. We believe the results from these studies will validate PROMETA as a method of care for treating alcoholism and stimulant dependence, as well as serve to accelerate our growth.

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Interest Income

Interest income increased from $834,000 in 2005 to $1.6 million in 2006 primarily due to higher average marketable securities balances from the proceeds of our $40 million equity offering in November 2005 and an increase in the weighted average interest rates during 2006.
Year Ended


Behavioral Health Managed Care Services

The following table summarizes the operating results for behavioral health managed care services for the period January 13 through December 31, 2005 Compared2007, which consisted entirely of the operations of CompCare subsequent to Year Ended December 31, 2004
Revenuesour acquisition of a majority controlling interest in CompCare on January 12, 2007 and related purchase accounting adjustments. CompCare’s operating results for prior periods are not included in our consolidated financial statements.
 
 
(Dollar amounts in thousands)
 For the period January 13
through December 31,
 
  2007 
Revenues  
Capitated contracts$35,226 
Non-capitated contracts 1,080 
Total revenues 36,306 
Operating Expenses   
Claims expense 29,041 
Other behavioral health managed care services expense 6,638 
Total healthcare operating expense 35,679 
General and administrative expenses 3,721 
Depreciation and amortization 923 
Loss from operations (4,017)
Other non-operating income, net 32 
Interest income 143 
Interest expense (263)
Loss before provision for income taxes$(4,105)
    
Total membership 1,025,000 
Medical Loss Ratio (1) 82%
(1)  Medical loss ratio reflects claims expenses as a percentage of revenue of capitated contracts.

Revenues
Revenues for the year endedperiod January 13 through December 31, 2005 increased to $1.22007 include $14.6 million from $192,000 for the year ended December 31, 2004. The increase in revenues is directly attributable to the increasing numbernew HMO client in Indiana now with 279,000 Medicaid recipients. This contract started on January 1, 2007, accounted for 40% of patients treatedbehavioral health managed care services revenues in 2007. The premiums for this agreement were based on actuarial assumptions on the level of utilization of benefits by members covered under this new managed care behavioral health program and have limited historical basis. The premiums based on these assumptions may be insufficient to cover the benefits provided and CompCare may be unable to obtain offsetting rate increases. Contract premiums have been set based on anticipated significant savings and on types of utilization management that may not be possible, which may cause disagreements with providers that divert management resources and that may have an adverse impact on our consolidated financial statements in future periods. To offset high utilization costs during 2007, CompCare is negotiating and believes it will receive a rate increase effective January 1, 2008, provided it complies with monthly performance measures it believes it will meet. The rate increase would amount to approximately $2.0 million per annum.
Operating Expenses

The medical loss ratio amounted to 82% for the period January 13 through December 31, 2007, and reflects increased member utilization during the months of March, April and May due to historical seasonality and from higher utilization of services by members during the initial months under the new contract with the Indiana HMO client. Providing services under a new contract for populations at our U.S. licensed sites. The total numberrisk that have not yet been managed previously


necessitates the adjustment to an increased  level of management and approval called for in the managed care agreements.  It typically takes time and resources to facilitate the adjustment to the new environment by our licensees was 216the providers and other participants in 2005the system.  As a result, higher utilization and related claims costs were incurred at the beginning of this contract compared to 40what we expect to incur in 2004. Our average license fees per patient at these sites also increased from $4,800 in 2004 to $5,337 in 2005,the future as the relative percentage of patients treated by our licensees who were offered partial or full discountspopulation becomes more accustomed to managed care. There has been higher utilization during the site start-up periodfirst year of the contract for services to members that were currently receiving treatment or had previously received treatment prior to the start of the contract. In response, CompCare hired additional personnel and contracted for training purposes declined in 2005 from 2004. There were no significant changes in our licensing fees chargedmore psychiatrist services. In addition, to our licensees betweenhelp better manage the periods.
Operating Expenses
     In 2005, our operating expenses increased to $26.0 million from $12.1 million incurredcare for new members seeking treatment, the higher amount of initial authorizations experienced in the previous year, as we expandedfirst month of the numbercontract were reduced so that the needs of licensees, increased ourthe members could be better evaluated.  All of these measures have reduced authorizations granted in subsequent months.  CompCare is taking additional steps to further increase management of this population, including working with providers to facilitate appropriate levels of care and support staff, commenced marketing and advertising our PROMETA protocols, funded clinical research studies and invested in development of international opportunities.
     Salaries and benefits expenses were $9.2 million and $5.1 millionmore strictly applying benefit definitions. Due to the factors discussed above, the medical loss ratio for this contract amounted to 100% for the years endedperiod January 13 through December 31, 20052007.  As discussed above, CompCare is negotiating and 2004, respectively.believes it will receive a rate increase effective January 1, 2008, provided it complies with monthly performance measures it believes it will meet. The rate increase in 2005 over 2004 reflects the increase in personnel from 37would amount to approximately 90 employees at the end$2.0 million per annum.
Other healthcare expenses, which are attributable to servicing both capitated and non-capitated contracts, were 18% of 2005, as we have added managers in the field to support our 32 licensed sites and have increased our corporate staff to support our rapid growth in operations, research, sales and marketing efforts, new business initiatives and general administrative functions.
     Other expenses were $13.2 million and $6.2 millionoperating revenue for the years endedperiod January 13 through December 31, 20052007.

General and 2004, respectively,administrative expenses for the period January 13 through December 31, 2007 reflect $416,000 in costs incurred as a result of the retirement of CompCare’s previous CEO, which included non-cash chargesrepresented two years of $1.7 millionbase salary pursuant to a change in control provision in her employment agreement. General and $1.2 million, respectively,administrative expenses for this period also reflect approximately $239,000 in costs and expenses resulting from the acquisition and proposed merger between Hythiam and CompCare, and for legal services in defense against two class action lawsuits related to the issuanceproposed merger that have subsequently been dismissed.

Depreciation and amortization for the period January 13 through December 31, 2007 includes $775,000 of common stock, stock options and warrants for services received from non employees. Other expenses include legal, audit, insurance, rent, travel and entertainment, investor relations, marketing, advertising, business developmentamortization related to the fair value attributable to managed care contracts and other professional consulting costs. Most expenditures increased significantly in 2005 from 2004, dueidentifiable intangible assets acquired as part of the CompCare acquisition.

Interest Expense

Interest expense relates to the rapid growth of our business and the overall increase in staffing and corporate infrastructure to support this growth. In addition, beginning in the second half of 2005, we invested significant funds in test piloting local advertising campaigns and the development of corporate advertising and marketing programs to increase public awareness of our PROMETA treatment, as well as development of a consumer website. We also incurred over $400,000 in 2005 for consultants and additional audit fees to meet the new internal control reporting requirements of Section 404 of the Sarbanes-Oxley Act of 2002.
     In 2005 we incurred approximately $2.6 million for research and development, compared to $177,000 in 2004, as we funded unrestricted grants for research studies to evaluate our PROMETA protocols, initiated a patient outcomes registry and commenced commercial pilot studies.
Interest Income
     The increase in interest income from $171,000 in 2004 to $834,000 in 2005 was primarily due to proceeds from our equity offerings of $21$2.0 million in 7.5% convertible subordinated debentures at CompCare and includes approximately $78,000 of amortization related to the purchase price allocation adjustment related to the CompCare acquisition for the period January 13 through December 2004 and $40 million in November 2005, and an increase in the weighted average interest rates during 2005.31, 2007.

35



Liquidity and Capital Resources

We have financed our operations, since inception, primarily through the sale of shares of our common stock in public and private placement stock offerings.  The following table sets forth a summary of our equity offering proceeds, net of expenses, since our inception (in millions):
       
Date Transaction Type Amount 
Sep 2003 Private Placement $21.3 
Dec 2004 Private Placement  21.3 
Nov 2005 Public Offering  40.2 
Dec 2006 Private Placement  24.4 
      
    $107.2 
      

DateTransaction TypeAmount
September 2003Private Placement $    21.3
December 2004Private Placement       21.3
November 2005Public Offering       40.2
December 2006Private Placement       24.4
November 2007Registered Direct Placment       42.8
 $  150.0

On November 7, 2007, we completed a registered direct placement, in which we issued an aggregate of 9,635,000 shares of common stock at a price of $4.79 per share, for gross proceeds of approximately $46.2 million, with select institutional investors. We also issued 5-year warrants to purchase an aggregate of approximately 2.4 million additional shares of our common stock at an exercise price of $5.75 per share. Included in the gross proceeds


was $5.35 million from the conversion of $5 million of the senior secured notes issued to Highbridge (see discussion below), which includes $350,000 based on a redemption price of 107% of the principal amount being redeemed pursuant to a redemption agreement entered into with Highbridge in November 2007. The fair value of the warrants at the date of issue was estimated at $6.3 million, accounted for as a liability in accordance with EITF 00-19.  We intend to use the proceeds of the registered direct common stock placement for working capital and general corporate purposes. We incurred approximately $3.4 million in fees to placement agents and other transaction costs in connection with the transaction, of which $1.2 million was accrued and payable at December 31, 2007.

In December 2006, we issued 3,573,2583,573,000 shares of common stock at a price of $7.30 per share in a closed private placement offering for a total of $26.1 million in proceeds from funds affiliated with existing investors and accredited institutional investors. At December 31, 2006, we owed approximatelyWe paid $1.8 million in placement fees to placement agents and other transaction costs,the underwriters in connection with the transaction.

In November 2005, we completed an underwritten equity offering of 9,200,000 shares at a price of $4.75 per share for a total of $43.7 million in proceeds.  We paid $3.1 million in placement fees to the underwriters in connection with the transaction.
     In December, 2004, we issued 5,017,331 shares of common stock at a price of $4.50 per share in a private placement offering for a total of $22.6
We received $10 million in proceeds from private investors, including two membersthe issuance of a secured note to finance the cash portion of our boardacquisition cost to acquire a controlling interest in CompCare, and we received an additional $2.0 million of directors who invested a totalproceeds from exercises of $1.2 million. We paid $1.2 million in fees to placement agents in connection withstock options and warrants during the transaction.year ended December 31, 2007.

As of December 31, 2006,2007, we had a balance of approximately $43.4$47.0 million in cash, cash equivalents and marketable securities.
     Since we are a rapidly growing business, our prior operating costs are not necessarily representativesecurities, of which approximately $6.3 million is held by CompCare. As of December 31, 2007, approximately $19 million of our expected future operating costs. Asmarketable securities consisted of auction rate securities, which are variable-rate instruments with longer stated maturities whose interest rates are reset at predetermined short-term intervals through a Dutch auction system. Through February 13, 2008, all of our auction rate securities held at December 31, 2007 had completed at least one auction successfully through the normal auction process, and we had reduced our total investments in auction rate securities to $11.5 million. However, from February 14 through March 12, 2008, auctions for these securities had failed, meaning the parties desiring to sell securities could not be matched with an adequate number of buyers, resulting in our having to continue to grow,hold these securities. Although the securities are Aaa/AAA rated and collateralized by portfolios of student loans guaranteed by the U.S. government, based on current market conditions it is likely that auctions will continue to be unsuccessful, limiting the short-term liquidity of these investments until the auction succeeds, the issuer calls the securities, or they mature.  As a result, our ability to liquidate our investment and fully recover the carrying value of our investment in the near term may be limited or not exist. If the issuers are unable to successfully close future auctions or their credit ratings deteriorate, we may in the future record an impairment charge on these investments. In addition, these types of developments could cause us to reclassify our investments in auction rate securities from a current asset to a long-term asset.  We believe that the higher reset rates on failed auctions provide sufficient incentive for the security issuers to address this lack of liquidity. While these failures in the auction process have affected our ability to access these funds in the near term, we do not believe that the underlying securities or collateral have been affected.  At this time, we have not obtained sufficient evidence to conclude that these investments are impaired or that they will not be settled in the short term, although the market for these investments is uncertain. We believe that we will not require access to these funds in the near-term prior to restoration of liquidity in this market. These securities will be analyzed each reporting period for other-than-temporary impairment factors. If the credit rating of the security issuers deteriorates, we may be required to adjust the carrying value of these investments through an impairment charge.
 In January 2008, we streamlined our operations to increase our focus on disease management and managed care opportunities, which is expected to result in an overall reduction of 25% to 30% of cash operating expenses for the fiscal year ending December 31, 2008. The actions we took included eliminating field and regional sales personnel and related corporate support personnel, closing the PROMETA Center in San Francisco,  a reduction in outside consultants and overall reductions in overhead costs.  Estimated one-time costs associated with these actions were approximately $1.0 million and will be recognized as a charge to operating expenses in the statement of operations for the quarter ended March 31, 2008. Such costs primarily represent severance and related benefits and costs incurred to close the San Francisco PROMETA Center. We do not expect to incur any material additional costs associated with this initiative. We also anticipate that in addition to previously entered into and announced business relationships, new disease management agreements from labor unions, self-insured employers, and managed care


health plans will add to the current private pay revenue base and result in higher revenues for 2008. The combination of increased revenues and cost reductions is expected to reduce the company's net cash utilization for 2008 compared to 2007. Following the streamlining actions taken in January 2008, we anticipate that our monthly cash operating expenditures will average approximately $2.5 million per month for the remainder of 2008 compared to steadily increase from our 2006an average of approximately $3.0$3.6 million per month to approximately $3.4 million per month in the fourth quarter of 2007,  excluding research and development costs and costs incurred by our newly consolidated subsidiary, CompCare, as discussed below. We plan to spend approximately $5.7$4.9 million in 20072008 for research and development. CompCare had positive net cash flow in 2007, principally due to new contracts that started January 1, 2007, but is expected to incur negative cash flows during 2008 resulting from increased claims expense. However, CompCare believes that it has sufficient cash reserves to sustain its current operations and to meet its obligations. Because of the significant publicly held minority interest in CompCare, we do not anticipate receiving dividends from CompCare or otherwise having access to cash flows generated by CompCare’s business.

In 2006 and 2007, we expended approximately $957,000 and $1.5 million, respectively, in capital expenditures for the build-out and equipping of the new PROMETA Center in San Francisco, the purchase of computers and office equipment for the increase in staff, expansion of our corporate office facilities and additional investments in the development of our information systems and other equipment needs. In 2007, weWe expect our capital expenditures to be approximately $700,000,$900,000 in 2008, primarily for the purchase of computer software related to our planned disease management products, computers and office equipment for an increase inour staff and additional investments in the development of our information systems, excluding capitalsystems. Capital spending relatedby CompCare in 2008 is not expected to CompCare, as discussed below.
be material. Our future capital requirements will depend upon many factors, including progress with our marketing our technologies,efforts, the time and costs involved in preparing, filing, prosecuting, maintaining and enforcing patent claims and other proprietary rights, the necessity of, and time and costs involved in obtaining, regulatory approvals, competing technological and market developments, and our ability to establish collaborative arrangements, effective commercialization, marketing activities and other arrangements.

We expect to continue to incur negative cash flows and net losses for at least the next twelve months. Based upon our current plans, including anticipated revenues, and increased expenses of expanding our business into managed care and government-sponsored programs, we believe that our existing cash, reserves totaling approximately $43.4 million as of December 31, 2006cash equivalents and marketable securities, together with the estimated proceeds from the November 7, 2007 offering discussed above, will be sufficient to meetfund our operating expenses and capital requirements until we achievegenerate positive cash flows, which we believe will be within the next two years.  Revenues may not increase as quickly as anticipated, and changes in our business strategy, technology development or marketing plans or other events affecting our operating plans and expenses may result in the expenditure of existing

36


cash before we achieve positive cash flow. If this occurs, ourOur ability to meet our cash obligations as they become due and payable will depend on our ability to delay or reduce operating expenses, sell securities, borrow funds or some combination thereof. We may also seek to raise additional fundingcapital through public or private financing or through collaborative arrangements with strategic partners. We may also seek to raise additional capital through public or private financing in order to increase the amount of our cash reserves on hand. We may not be successful in raising necessary funds on acceptable terms, or at all.  If this occurs, and we do not or are unable to borrow funds or sell additional securities, we may be unable to meet our cash obligations as they become due and we may be required to delay or reduce operating expenses and curtail our operations, which would have a material adverse effect on us.

CompCare Acquisition and Financing

In January 2007, we acquired all of the outstanding membership interests of Woodcliff Healthcare Investment Partners, LLC (Woodcliff) for $9 million in cash and 215,053approximately 215,000 shares of our common stock. Woodcliff owns 1,739,1301,739,000 shares of common stock and 14,400 shares of Series A Convertible Preferred Stock of Comprehensive Care Corporation, a Delaware corporation (CompCare),CompCare, the conversion of which would result in Woodcliffus owning over 50% the outstanding shares of common stock of CompCare. The preferred stock has voting rights and, combined with the common shares held by Woodcliff,us, gives us voting control over CompCare.  The preferred stock gives us significant rights, and preferences over the minority holders of CompCare’s common stock, including:

·      the right to appoint five membersdesignate the majority of CompCare’s board of directors which represents the majority of its directors
·      dividend and liquidation preferences, and

·      anti-dilution protection.



In addition, without our consent, CompCare is prevented from engaging in any of the following transactions:
·      any sale or merger involving a material portion of assets or business

·      any single or series of related transactions in excess of $500,000, and

·      incurring any debt in excess of $200,000.
     Following our acquisition of Woodcliff, in January 2007, we entered into an Agreement and Plan of Merger with CompCare, with CompCare to survive after the proposed merger as our wholly-owned subsidiary. Pursuant to the merger agreement, we would acquire the remaining outstanding shares of common stock of CompCare in exchange for shares of our common stock. If pending litigation is not quickly resolved on reasonable terms, we may elect with CompCare to terminate the merger agreement and not proceed with the merger.
In January 2007, to finance the WoodcliffCompCare acquisition, we entered into a Securities Purchase Agreementsecurities purchase agreement pursuant to which we sold to Highbridge International LLC (a) $10 million original principal amount of senior secured notes and (b) warrants to purchase up to 249,750approximately 250,000 shares of our common stock.stock (adjusted to 285,000 shares as of December 31, 2007). The note bears interest at a rate of prime plus 2.5%, interest payable quarterly commencing on April 15, 2007, and matures on January 15, 2010, with an option offor Highbridge to demand redemption of the Notes after 18 months from the date of issuance.

In connection with the debt financing, we entered into a security agreement granting Highbridge a first-priority perfected security interest in all of our assets now owned or thereafter acquired. We also entered into a pledge agreement with Highbridge, as collateral agent, pursuant to which we will deliver equity interests evidencing 65% of our ownership of our foreign subsidiaries. In the event of a default, the collateral agent is given broad powers to sell or otherwise deal with the pledged collateral.

As discussed above, we redeemed $5 million in principal related to the senior secured notes on November 7, 2007.

The acquisition of Woodcliff and a majority controlling interest in CompCare isdid not expected to require any material amount of additional cash investment or expenditures by us in 2007, by us,and is not expected to do so in 2008, other than expenditures expected to be made by CompCare from its existing cash reserves and cash flow from its operations.

The unpaid claims liability for managed care services is estimated using an actuarial paid completion factor methodology and other statistical analyses.  These estimates are subject to the effects of trends in utilization and other factors.  Any significant increase in member utilization that falls outside of our estimations would increase healthcare operating expenses and may impact the ability for these plans to achieve and sustain profitability and positive cash flow. Although considerable variability is inherent in such estimates, we believe that the unpaid claims liability is adequate. However, actual results could differ from the $5.5 million claims payable amount reported as of December 31, 2007.

Legal Proceedings

From time to time, we may be involved in litigation relating to claims arising out of our operations in the normal course of business.  Aside from the CompCare stockholder litigation discussed in Item 3, “Legal Proceedings,” asAs of the date of this report, we are not currently involved in any legal proceeding that we believe would have a material adverse effect on our business, financial condition or operating results.

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Contractual Obligations and Commercial Commitments

The following table sets forth a summary of our material contractual obligations and commercial commitments as of December 31, 20062007 (in thousands):
                     
      Less than 1          More than 5 
Contractual Obligations Total  year ��1 - 3 years  3 - 5 years  years 
Operating lease obligations (1) $4,912  $1,158  $2,435  $1,316  $3 
Contractual commitments for clinical studies  5,900   5,185   715       
Capital lease obligations  292   67   133   92    
Other Liabilities  94   47   47       
                
  $11,198  $6,457  $3,330  $1,408  $3 
                

Contractual Obligations Total Less than 1 year 1 - 3 years 3 - 5 years More than 5 years
Long-term debt obligations, including interest $8,434 $5,290 $3,144 $- $-
Claims payable (1)  5,464  5,464  -  -  -
Reinsurance claims payable (2)  2,526  -  2,526  -  -
Capital lease obligations  607  231  297  79  -
Operating lease obligations (3)  4,643  1,624  2,611  408  -
Contractual commitments for clinical studies  4,150  4,150  -  -  -
  $25,824 $16,759 $8,578 $487 $-

(1)  These claim liabilities represent the best estimate of benefits to be paid under capitated contracts and consist of reserves for claims and IBNR. Because of the nature of such contracts, there is typically no minimum contractual commitment associated with covered claims. Both the amounts and timing of such payments are estimates, and the actual claims paid could differ from the estimated amounts presented.
(2)  This item represents a liability relating to denied claims for a terminated reinsurance contract. Any adjustment to the reinsurance claims liability subsequent to December 31, 2007 would be accounted for in our statement of operations in the period in which the adjustment is determined.
(1)(3)  Operating lease commitments for our and CompCare’s corporate office facilities, and two PROMETA Centers, including deferred rent liability.liability, a managed treatment center in Dallas, Texas and facilities related to our international operations.

Off-Balance Sheet Arrangements

As of December 31, 2006,2007, we had no off-balance sheet arrangements.

Effects of Inflation

 Our most liquid assets are cash, cash equivalents and marketable securities. Because of their liquidity, these assets are not directly affected by inflation. Because we intend to retain and continue to use our equipment, furniture and fixtures and leasehold improvements, we believe that the incremental inflation related to replacement costs of such items will not materially affect our operations. However, the rate of inflation affects our expenses, such as those for employee compensation and contract services, which could increase our level of expenses and the rate at which we use our resources.

Critical Accounting Estimates

The discussion and analysis of our financial condition and results of operations is based upon our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States. Generally accepted accounting principles require management to make estimates, judgments and assumptions that affect the reported amounts of assets, liabilities, revenues and expenses, and the disclosure of contingent assets and liabilities. We base our estimates on experience and on various other assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that may not be readily apparent from other sources. On an on-going basis, we evaluate the appropriateness of our estimates and we maintain a thorough process to review the application of our accounting policies.  Our actual results may differ from thosethese estimates.

We consider our critical accounting estimates to be those that (1) involve significant judgments and uncertainties, (2) require estimates that are more difficult for management to determine, and (3) may produce materially different results when using different assumptions. Management hasWe have discussed these critical accounting estimates,


the basis for their underlying assumptions and estimates and the nature of our related disclosures herein with the audit committee of our board of directors. Our criticalWe believe our accounting policies specific to behavioral health managed care services revenue recognition, managed care premium deficiencies, accrued claims payable and claims expense for managed care services, share-based compensation expense and the impairment assessments for goodwill and other intangible assets involve our most significant judgments and estimates coverthat are material to our consolidated financial statements. They are discussed further below:

Managed Care Services Revenue Recognition

We provide managed behavioral healthcare and substance abuse services to recipients, primarily through subcontracts with HMOs.  Revenue under the following areas:vast majority of these agreements is earned and recognized monthly based on the number of covered members as reported to us by our clients regardless of whether services actually provided are lesser or greater than anticipated when we entered into such contracts (generally referred to as capitation arrangements). The information regarding qualified participants is supplied by CompCare’s clients and CompCare reviews membership eligibility records and other reported information to verify its accuracy in determining the amount of revenue to be recognized. Consequently, the vast majority of our revenue is determined by the monthly receipt of covered member information and the associated payment from the client, thereby removing uncertainty and precluding us from needing to make assumptions to estimate monthly revenue amounts.
Share-based Compensation Expense
We may experience adjustments to our revenues to reflect changes in the number and eligibility status of members subsequent to when revenue is recognized.  Subsequent adjustments to our revenue have not been material.

Premium Deficiencies

CompCare accrues losses under capitated contracts when it is probable that a loss has been incurred and the amount of the loss can be reasonably estimated. CompCare performs this loss accrual analysis on a specific contract basis taking into consideration such factors as future contractual revenue, projected future healthcare and maintenance costs, and each contract's specific terms related to future revenue increases as compared to expected increases in healthcare costs. The projected future healthcare and maintenance costs are estimated based on historical trends and our estimate of future cost increases.

At any time prior to the end of a contract or contract renewal, if a capitated contract is not meeting its financial goals, CompCare generally has the ability to cancel the contract with 60 to 90 days written notice.  Prior to cancellation, CompCare will usually submit a request for a rate increase accompanied by supporting utilization data.  Although CompCare’s clients have historically been generally receptive to such requests, no assurance can be given that such requests will be fulfilled in the future in CompCare’s favor.  If a rate increase is not granted, CompCare has the ability to terminate the contract and limit its risk to a short-term period.

On a quarterly basis, CompCare performs a review of its portfolio of contracts for the purpose of identifying loss contracts (as defined in the American Institute of Certified Public Accountants Audit and Accounting Guide – Health Care Organizations) and developing a contract loss reserve, if applicable, for succeeding periods. During the period January 13 through December 31, 2007, CompCare identified two contracts that were not meeting their financial goals. CompCare successfully obtained a rate increase from one client effective January 1, 2008. CompCare is negotiating and believes it will receive a rate increase from the other client effective January 1, 2008, provided it complies with monthly performance measures it believes it will meet. The rate increase would amount to approximately $2.0 million per annum. At December 31, 2007, CompCare believes no contract loss reserve for future periods is necessary for these contracts.
 
Accrued Claims Payable and Claims Expense

Behavioral health managed care operating expenses are composed of claims expense and other healthcare expenses.  Claims expense includes amounts paid to hospitals, physician groups and other managed care organizations under capitated contracts. Other healthcare expenses include items such as information systems, provider contracting, case management and quality assurance, attributable to both capitated and non-capitated contracts.




The cost of behavioral health services is recognized in the period in which an eligible member actually receives services and includes an estimate of IBNR. CompCare contracts with various healthcare providers including hospitals, physician groups and other managed care organizations either on a discounted fee-for-service or a per-case basis.  CompCare determines that a member has received services when it receives a claim within the contracted timeframe with all required billing elements correctly completed by the service provider.  CompCare then determines whether (1) the member is eligible to receive such services, (2) the service provided is medically necessary and is covered by the benefit plan’s certificate of coverage, and (3) the service has been authorized by one of CompCare’s employees.  If all of these requirements are met, the claim is entered into CompCare’s claims system for payment and the associated cost of behavioral health services is recognized. If the claim is denied, the service provider is notified and has appeal rights under their contract with us.

Accrued claims payable consists primarily of CompCare’s reserves established for reported claims and claims that have been incurred but not reported (IBNR), which are unpaid through the respective balance sheet dates. CompCare’s policy is to record management’s best estimate of IBNR. The IBNR liability is estimated monthly using an actuarial paid completion factor methodology and is continually reviewed and adjusted, if necessary, to reflect any change in the estimated liability as more information becomes available. In deriving an initial range of estimates, CompCare’s management uses an actuarial model that incorporates past claims payment experience, enrollment data and key assumptions such as trends in healthcare costs and seasonality. Authorization data, utilization statistics, calculated completion percentages and qualitative factors are then combined with the initial range to form the basis of management’s best estimate of the accrued claims payable balance.

At December 31, 2007, CompCare’s management determined its best estimate of the accrued claims liability to be $5.5 million. Approximately $2.3 million of the $5.5 million accrued claims payable balance at December 31, 2007 is attributable to the new major HMO contract in Indiana that started January 1, 2007.  As of December 31, 2007 CompCare has accrued as claims expense approximately 100% of the revenue from this contract. Due to limited historical claims payment data, CompCare’s management estimated the IBNR for this contract primarily by using estimated completion factors based on authorization data.

Accrued claims payable at December 31, 2007 comprises approximately $1.1 million of submitted and approved claims, which had not yet been paid, and $4.4 million for IBNR claims.

Many aspects of the managed care business are not predictable with consistency, and therefore, estimating IBNR claims involves a significant amount of management judgment.  Actual claims incurred could differ from the estimated claims payable amount presented.  The following are factors that would have an impact on CompCare’s future operations and financial condition:

·      Changes in utilization patterns
·      Changes in healthcare costs
·      Changes in claims submission timeframes by providers
·      Success in renegotiating contracts with healthcare providers
·      Adverse selection
·      Changes in benefit plan design
·      The impact of present or future state and federal regulations
A 5% increase or decrease in assumed healthcare cost trends from those used in the calculations of IBNR at December 31, 2007, could increase or decrease CompCare’s claims expense by approximately $193,000.



Share-based expense

Commencing January 1, 2006, we implemented the accounting provisions of SFAS 123R on a modified-prospective basis to recognize share-based compensation for employee stock option awards in our statements of operations for future periods. We accountaccounted for the issuance of stock, options to employees and directors in accordance with SFAS 123R and the issuance of stock options and warrants for services from non-employees in accordance with SFAS 123, “Accounting for Stock-Based Compensation,Compensation.” and the Financial Accounting Standards Board (FASB)FASB Emerging Issues Task Force Issue (EITF) No. 96-18, “Accounting For Equity Instruments That Are Issued To Other Than Employees For Acquiring Or In Conjunction With Selling Goods Or Services,Services.by estimatingWe estimate the fair value of

38


options and warrants issued using the Black-Scholes pricing model. This model’s calculations include the exercise price, the market price of shares on grant date, weighted average assumptions for risk-free interest rates, expected life of the option or warrant, expected volatility of our stock and expected dividend yield.

The amounts recorded in the financial statements for share-based expense could vary significantly if we were to use different assumptions. For example, the assumptions we have made for the expected volatility of our stock price have been made using, in part,based on the historical volatility averagesof our stock and the stock of other public healthcare companies, measured over a period generally commensurate with the expected term, since we have a limited history as a public company and complete reliance on our actual stock price volatility would not be meaningful. If we were to use the actual volatility of our stock price, there may be a significant variance in the amounts of share-based expense from the amounts reported. Based on the 20062007 assumptions used for the Black-Scholes pricing model, a 50% increase in stock price volatility would have increased the fair values of options by approximately 25%. The weighted average expected option term for 2007 and 2006 reflects the application of the simplified method set out in SEC Staff Accounting Bulletin No. 107, which defines the life as the average of the contractual term of the options and the weighted average vesting period for all option tranches.

Goodwill

We evaluate goodwill for impairment annually based on the estimated fair value of our healthcare services reportable segment. We test for impairment on a more frequent basis in cases where events and changes in circumstances would indicate that we might not recover the carrying value of goodwill. In estimating the fair value, management considers both the income and market approaches to fair value determination. The income approach is based on a discounted cash flow methodology, in which management makes its best assumptions regarding future cash flows and a discount rate to be applied to the cash flows to yield a present, fair value of the reporting unit. The market approach is based primarily on reference to transactions involving the company’s common stock and the quoted market prices of the company’s common stock. As a result of such tests, management believes there is no material risk of loss from impairment of goodwill.  However, actual results may differ significantly from management’s assumptions, resulting in potentially adverse impact to our consolidated financial statements.

Impairment of Intangible Assetsintangible assets

We have capitalized significant costs, and plan to capitalize additional costs, for acquiring patents and other intellectual property directly related to our products and services. We will continue to evaluate our intangible assets for impairment on an ongoing basis by assessing the future recoverability of such capitalized costs based on estimates of our future revenues less estimated costs. Since we have not recognized significant revenues to date, our estimates of future revenues may not be realized and the net realizable value of our capitalized costs of intellectual property may become impaired. In December 2005, we recorded an impairment charge of $272,000 to write off the capitalized costs of intellectual property relating to an acquired patent for a treatment method for opiate addiction that we have determined would not likely be utilized in our current business plan. As a result of a non-cash stock settlement agreement reached in August 2007 with seller of the opiate patent, we released 310,000 shares of our common stock, which shares had been subject to a stock pledge agreement pending the resolution of certain contingencies, as additional consideration related to the purchase of the patent. The fair market value of these shares amounted to $2.4 million, based on the closing stock price on the date of the settlement, and was recorded as an additional impairment loss for the year ended December 31, 2007. We recorded no impairment charges in 2006.



Recent Accounting Pronouncements
     In June 2006, the FASB issued FASB Interpretation No. 48, “Accounting for Uncertainty in Income Taxes,” (FIN 48) which clarifies the accounting for uncertainty in income taxes. FIN 48 requires that companies recognize in the consolidated financial statements the impact of a tax position, if that position is more likely than not of being sustained on audit, based on the technical merits of the position. FIN 48 also provides guidance on derecognition, classification, interest and penalties, accounting in interim periods and disclosure. The provisions of FIN 48 are effective for fiscal years beginning after December 15, 2006. We will adopt FIN 48 effective January 1, 2007. We are currently evaluating the effect of this new pronouncement.
In September 2006, The FASB issued SFAS No. 157, “Fair Value Measurements,” (SFAS 157)SFAS 157 which defines fair value, establishes a framework for measuring fair value in generally accepted accounting principles, and expands disclosures about fair value measurements. The statement is effective for financial statements issued for fiscal years beginning after November 15, 2007, and interim periods within those fiscal years. We are currently evaluating the statementThe adoption of SFAS No. 157 is not expected to determine what, if any,have a material impact it will have on our consolidated financial statements.position, results of operations or cash flows.

In November 2006,February 2007, the FASB issued FASB Staff PositionSFAS No. EITF 00-19-2, “Accounting159, "The Fair Value Option for Registration Payment Arrangements”, which specifiesFinancial Assets and Financial Liabilities" ("SFAS 159"). SFAS 159 allows companies to measure many financial assets and liabilities at fair value. It also establishes presentation and disclosure requirements designed to facilitate comparisons between companies that the contingent obligation to make future payments or otherwise transfer consideration under a registration payment arrangement, whether issued as a separate agreement or included as a provisionchoose different measurement attributes for similar types of a financial instrument or other agreement, should be separately recognizedassets and measured. Additionally, this guidance further clarifies that a financial instrument subject to a registration payment arrangement should be accounted for in accordance with other applicable GAAP without regard to the contingent obligation to transfer consideration pursuant to the registration payment arrangement. This guidanceliabilities. SFAS 159 is effective for financial statements issued for fiscal years beginning after DecemberNovember 15, 2006,2007 and interim periods within those fiscal years. We have chosen an earlyThe adoption of this guidance effective for the fourth quarter of 2006 without a material impact to our consolidated financial statements.
     In February 2007, the FASB issued StatementSFAS No. 159 “The Fair Value Option for Financial Assets and Financial Liabilities” (SFAS 159). SFAS 159 provides that companies may elect to measure specified financial instruments and warranty and insurance contracts at fair value on a contract-by-contract basis, with changes in fair value recognized in earnings each reporting period. The election, called the “fair value option,” will enable some companies to reduce the variability in reported earnings caused by measuring related assets and liabilities differently. Companies may elect fair-value measurement when an eligible asset or liability is initially recognized or

39


when an event, such as a business combination, triggers a new basis of accounting for that asset or liability. The election is irrevocable for every contract chosen to be measured at fair value and must be applied to an entire contract, not to only specified risks, specific cash flows, or portions of that contract. SFAS 159 is effective as of the beginning of a company’s first fiscal year that begins after November 15, 2007. Retrospective application is not allowed. Companies may adopt SFAS 159 as of the beginning of a fiscal year that begins on or before November 15, 2007 if the choiceexpected to adopt early is made after SFAS 159 has been issued and within 120 days of the beginning of the fiscal year of adoption and the entity has not issued GAAP financial statements for any interim period of the fiscal year that includes the early adoption date. Companies are permitted to elect fair-value measurement for any eligible item within SFAS 159’s scope at the date they initially adopt SFAS 159. The adjustment to reflect the difference between the fair value and the current carrying amount of the assets and liabilities for which a company elects fair-value measurement is reported as a cumulative-effect adjustment to the opening balance of retained earnings upon adoption. Companies that adopt SFAS 159 early must also adopt all of SFAS 157’s requirements at the early adoption date. We are assessing the impact of adopting SFAS 159 and currently do not believe the adoption will have a material impact on our financial position, results of operations or cash flows.

In December 2007, the FASB issued SFAS No. 141(R), "Business Combinations" ("SFAS 141(R)"). SFAS 141(R) replaces SFAS No. 141, "Business Combinations", but retains the requirement that the purchase method of accounting for acquisitions be used for all business combinations. SFAS 141(R) expands on the disclosures previously required by SFAS 141, better defines the acquirer and the acquisition date in a business combination, and establishes principles for recognizing and measuring the assets acquired (including goodwill), the liabilities assumed and any non-controlling interests in the acquired business. SFAS 141(R) also requires an acquirer to record an adjustment to income tax expense for changes in valuation allowances or uncertain tax positions related to acquired businesses. SFAS 141(R) is effective for all business combinations with an acquisition date in the first annual period following December 15, 2008; early adoption is not permitted. We will adopt this statement as of January 1, 2009. We are currently evaluating the impact SFAS 141(R) will have on our consolidated financial statements.

In December 2007, the FASB issued SFAS No. 160, "Noncontrolling Interests in Consolidated Financial Statements—an amendment of ARB No. 51" ("SFAS 160"). SFAS 160 requires that non-controlling (or minority) interests in subsidiaries be reported in the equity section of the company's balance sheet, rather than in a mezzanine section of the balance sheet between liabilities and equity. SFAS 160 also changes the manner in which the net income of the subsidiary is reported and disclosed in the controlling company's income statement. SFAS 160 also establishes guidelines for accounting for changes in ownership percentages and for deconsolidation. SFAS 160 is effective for financial statements for fiscal years beginning on or after December 1, 2008 and interim periods within those years. The adoption of SFAS 160 is not expected to have a material impact on our financial position, results of operations or cash flows.

ITEM 7A.                  QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

We invest our cash in short term high grade commercial paper, certificates of deposit, money market accounts and marketable securities. We consider any liquid investment with an original maturity of three months or less when purchased to be cash equivalents. We classify investments with maturity dates greater than three months when purchased as marketable securities, which have readily determined fair values and are classified as available-for-sale securities. Our investment policy requires that all investments be investment grade quality and no more than ten percent of our portfolio may be invested in any one security or with one institution. At

As of December 31, 2006,2007, approximately $19 million of our investment portfoliomarketable securities consisted primarily of auction rate securities, which are reportedvariable-rate instruments with longer stated maturities whose interest rates are reset at predetermined short-term intervals through a Dutch auction system. Through February 13, 2008, all of our auction rate securities held at December 31, 2007 had completed at least one auction successfully through the normal auction process, and we had reduced our total investments in auction rate securities to $11.5 million. However, from February 14 through March 12, 2008, auctions for these securities had failed, meaning the parties desiring to sell securities could not be matched with an adequate number of buyers, resulting in our having to continue to hold these securities. Although the securities are Aaa/AAA rated and collateralized by portfolios of student loans guaranteed by the U.S. government, based on current market conditions it is likely that auctions will continue to be unsuccessful,


limiting the consolidated balance sheets as marketableshort-term liquidity of these investments until the auction succeeds, the issuer calls the securities, at paror they mature.  As a result, our ability to liquidate our investment and fully recover the carrying value which also equalsof our investment in the near term may be limited or not exist. If the issuers are unable to successfully close future auctions or their credit ratings deteriorate, we may in the future record an impairment charge on these investments. In addition, these types of developments could cause us to reclassify our investments in auction rate securities from a current asset to a long-term asset.  We believe that the higher reset rates on failed auctions provide sufficient incentive for the security issuers to address this lack of liquidity. While these failures in the auction process have affected our ability to access these funds in the near term, we do not believe that the underlying securities or collateral have been affected.  At this time, we have not obtained sufficient evidence to conclude that these investments are impaired or that they will not be settled in the short term, although the market for these investments is uncertain. We believe that we will not require access to these funds in the near-term prior to restoration of liquidity in this market. These securities will be analyzed each reporting period for other-than-temporary impairment factors. If the credit rating of the security issuers deteriorates, we may be required to adjust the carrying value as the rate on such securities resets generally every 7, 28 or 35 days. of these investments through an impairment charge.

The weighted average interest rate of marketable securities held at December 31, 20062007 was 5.3%5.49%.
 Investments in both fixed rate and floating rate interest earning instruments carry a degree of interest rate risk arising from changes in the level or volatility of interest rates; however interest rate movements do not materially affect the market value of our auction rate securities because of the frequency of the rate resets and the short-term nature of these investments. A reduction in the overall level of interest rates may produce less interest income from our investment portfolio. If overall interest rates had declined by an average of 100 basis points during 2006,2007, the amount of interest income earned from our investment portfolio in 20062007 would have decreased by an estimated amount of $333,000. $368,000The market risk associated with our investments in debt securities is substantially mitigated by the frequent turnover of our portfolio.

ITEM 8.                  FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA

Our consolidated financial statements and related financial information required to be filed hereunder are indexed under Item 15 of this report and are incorporated herein by reference.

ITEM 9.                  CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE
     Not applicable.
None.

ITEM 9A.               CONTROLS AND PROCEDURES

Disclosure Controls

We have evaluated, with the participation of our chief executive officer and our chief financial officer, the effectiveness of our system of disclosure controls and procedures as of the end of the period covered by this report. Based on this evaluation our chief executive officer and our chief financial officer have determined that they are effective in connection with the preparation of this report.

40



Management’sManagement's Report on Internal Control over Financial Reporting

Our management is responsible for establishing and maintaining adequate internal control over financial reporting (as defined in Rule 13a-15(f) under the Exchange Act) and for assessing the effectiveness of our internal control over financial reporting. Our internal control system is designed to provide reasonable assurance to our management and board of directors regarding the preparation and fair presentation of published financial statements in accordance with United States generally accepted accounting principles (GAAP).

There were no changes in our internal controls over financial reporting during the quarteryear ended December 31, 20062007 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.



Our internal control over financial reporting is supported by written policies and procedures that:

·      pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of our assets;

·      provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with GAAP and that our receipts and expenditures are being made only in accordance with authorizations of our management and our board of directors; and

·      provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of our assets that could have a material effect on our financial statements.

Our management assessed the effectiveness of our internal control over financial reporting as of December 31, 20062007 using the criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission inInternal Control-Integrated Framework. Management’sManagement's assessment included an evaluation of the design of our internal control over financial reporting and testing of the operational effectiveness of our internal control over financial reporting. Based on this assessment, our management concluded that, as of December 31, 2006,2007, our internal control over financial reporting was effective.

Because of its inherent limitations, a system of internal control over financial reporting can provide only reasonable assurance and may not prevent or detect misstatements. In addition, projections of any evaluation of effectiveness to future periods are subject to the risks that controls may become inadequate because of changes in conditions and that the degree of compliance with the policies or procedures may deteriorate.

BDO Seidman, LLP, the independent registered public accounting firm that audited the financial statements included in this Annual Report on Form 10-K, was engaged to attest to and report on management’s assessment of the effectiveness of our internal control over financial reporting as of December 31, 2006.2007. A copy of this report is included at page F-3 of this Annual Report on Form 10-K.

ITEM 9B.                 OTHER INFORMATION

Not applicable.

41








The information required by Items 10 through 14 of Part III is incorporated by reference from Item 1 of this report and from registrants’ proxy statement that will be mailed to stockholders in connection with the registrant’s 20062008 annual meeting of stockholders.

42





PART IV

ITEM 15.                      EXHIBITS, FINANCIAL STATEMENT SCHEDULES

(a)(1),(2)Financial Statements

The Financial Statements and Financial Statement Schedules listed on page F-1 of this document are filed as part of this filing.

(a)(3)Exhibits

The following exhibits are filed as part of this report:
 
Exhibit No. Description
3.1 
Certificate of Incorporation of Hythiam, Inc., a Delaware corporation, filed with the Secretary of State of Delaware on September 29, 2003(1)
 
3.2 
By-Laws of Hythiam, Inc., a Delaware corporation(1)
 
4.1 
Specimen Common Stock Certificate(3)
 
10.1* 
2003 Stock Incentive Plan(1)
 
10.2* 
Employment Agreement of Terren S. Peizer(3)
 
10.3* 
Employment Agreement of Richard A. Anderson(3)
 
10.4*Employment Agreement of Anthony LaMacchia(3)
10.5*Employment Agreement of Chuck Timpe(3)
10.6* 
Management and Support Services Agreement between Hythiam, Inc. and David E. Smith, M.D. Medical Group, Inc. (3)
 
10.7* 
Consulting Services Agreement between Hythiam, Inc. and David E. Smith & Associates(3)
 
10.8* 
First Amendment to Consulting Services Agreement between Hythiam, Inc. and David E. Smith, M.D. Medical Group, Inc. (4)
 
10.9* 
First Amendment to Management and Support Services Agreement Services Agreement between Hythiam, Inc. and David E. Smith, M.D. Medical Group, Inc. (4)
 
10.10* 
Second Amendment to Management and Support Services Agreement Services Agreement between Hythiam, Inc. and David E. Smith, M.D. Medical Group, Inc. (4)
 
10.11* 
Employment Agreement of Christopher Hassan(4)
 10.12* 
2007 Stock Incentive Plan(5)
10.13Form of Standard Technology License and Administrative Services Agreement
10.14*Second Amendment to Consulting Services Agreement between Hythiam, Inc. and David E. Smith, M.D. Medical Group, Inc.
10.15Redemption Agreement between Hythiam, Inc. and Highbridge International, LLC.
14.1 
Code of Conduct and Ethics(2)
 
14.2 
Code of Ethics for CEO and Senior Financial Officers(2)
 
21.1 Subsidiaries of the Company
 
23.1 Consent of Independent Registered Public Accounting Firm BDO Seidman, LLP
 23.2 Consent of Independent Valuation Specialist – Actuarial Risk Management
31.1 Certification by the Chief Executive Officer, pursuant to Rule 13-a-14(a)13a-14(a) and 15d-14(a)Rule 15d14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
 
31.2 Certification by the Chief Financial Officer, pursuant to Rule 13-a-14(a)13a-14(a) and 15d-14(a)Rule 15d14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
 
32.1 Certification by the Chief Executive Officer, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 
32.2 Certification by the Chief Financial Officer, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 

(1)  (1)Incorporated by reference to exhibit of the same number to the registrant’s Form 8-K filed September 30, 2003.
(2)(2)
Incorporated by reference to exhibit of the same number to the registrant’s annual report on Form 10-K for the year ended December 31, 2003.
 
(3) Incorporated by reference to exhibit of the same number to the registrant’sregistrant's annual report on Form 10-K for the year ended December 31, 2005.


 
(4)  Incorporated by reference to exhibit of the same number to the registrant's annual report on Form 10-K for the year ended December 31, 2006.
* Management contract or compensatory plan or arrangement.
(5)  Incorporated by reference to the registrant's Revised Definitive Proxy on Form DEFR14A filed May 11, 2007.

43


SIGNATURES
      *   Management contract or compensatory plan or arrangement.

SIGNATURES

Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
    
 
HYTHIAM, INC.
Date: March 15, 2007 17, 2008By:  /s/ TERREN S. PEIZER  
  Terren S. Peizer 
  President and Chief Executive Officer 

44




POWER OF ATTORNEY

Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed by the following persons on behalf of the registrant and in the capacities and on the dates indicated.

SignatureTitle(s)Date
     
SignatureTitle(s)Date
/s/ TERREN S. PEIZER Chairman of the Board of Directors and Chief
Terren S. Peizer
Executive Officer (Principal Executive Officer) March 15, 200717, 2008
   Terren S. Peizer
     
/s/ CHUCK TIMPE Chief Financial Officer (Principal Financial Officer) March 15, 200717, 2008
Chuck Timpe
    
     
/s/ MAURICE HEBERT Corporate Controller (Principal Accounting Officer) March 15, 200717, 2008
Maurice Hebert
    
     
/s/ RICHARD A. ANDERSON Director and Senior Executive Vice President March 15, 200717, 2008
Richard A. Anderson
    
     
/s/ ANTHONY M. LAMACCHIACHRISTOPHER S. HASSAN  Director and Senior Executive Vice President March 15, 200717, 2008
Anthony M. LaMacchia
  Christopher S. Hassan
    
     
/s/ LESLIE F. BELL, ESQ.  Director March 15, 200717, 2008
Leslie F. Bell,
Esq.
    
     
/s/ HERVÉ DE KERGROHENKAREN FREEMAN-WILSON Director March 15, 200717, 2008
Hervé de Kergrohen
  Karen Freeman-Wilson
    
     
/s/ IVAN M. LIEBERBURG, PH.D., M.D. Director March 15, 200717, 2008
Ivan M. Lieberburg,
Ph.D., M.D.
    
     
/s/ MARC G. CUMMINS Director March 15, 200717, 2008
Marc G. Cummins
    
     
/s/ ANDREA GRUBB BARTHWELL, M.D.  Director March 15, 200717, 2008
Andrea Grubb Barthwell,
M.D.
    

45






HYTHIAM, INC. AND SUBSIDIARIES
Index to Financial Statements and Financial Statement Schedules

Financial Statements

Financial Statement Schedules

All financial statement schedules are omitted because they are not applicable, not required, or the information is shown in the Financial Statements or Notes thereto.

F-1








Report of Independent Registered Public Accounting Firm
To the Board of Directors and Stockholders
Shareholders
Hythiam, Inc.
Los Angeles, California
We have audited the accompanying consolidated balance sheets of Hythiam, Inc. and subsidiaries (the Company) as of December 31, 20062007 and 20052006 and the related consolidated statements of operations, stockholders’ equity, and cash flows for each of the three years in the period ended December 31, 2006.2007.  These financial statements are the responsibility of the Company’s management.  Our responsibility is to express an opinion on these financial statements based on our audits.
We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States).  Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement.  An audit also includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements, assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation.  We believe that our audits provide a reasonable basis for our opinion.
In our opinion, suchthe consolidated financial statements referred to above present fairly, in all material respects, the financial position of Hythiam, Inc. and subsidiaries as ofthe Company at December 31, 2007 and 2006, and 2005 and the consolidated results of its operations and its cash flows for each of the three years in the period ended December 31, 2006,2007, in conformity with accounting principles generally accepted in the United States of America.
As more fully described in Note 1 to the consolidated financial statements, effective January 1, 2006, the Company adopted the provisions of Statement of Financial Accounting Standards No. 123R,Standard No.123 (R), “Share-Based Payment.”
We also have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the effectiveness of the Company’s internal control over financial reporting as of December 31, 2006,2007, based on the criteria established inInternal Control—Control – Integrated Frameworkissued by the Committee of Sponsoring Organizations of the Treadway Commission (COSO) and our report dated March 14, 20072008 expressed an unqualified opinion thereon.
/s/ BDO Seidman, LLP


Los Angeles, California
March 14, 20072008

F-2





Report of Independent Registered Public Accounting Firm

To the Stockholders and Board of Directors
and Shareholders
Hythiam, Inc.
Los Angeles, California
We have audited management’s assessment, included inManagement’s Report on Internal Control over Financial Reportingappearing in Item 9A of the accompanying Annual Report on Form 10-K, that Hythiam, Inc. and subsidiariessubsidiaries’ (the Company) maintained effective internal control over financial reporting as of December 31, 2006,2007, based on criteria established inInternal Control-IntegratedControl – Integrated Frameworkissued by the Committee of Sponsoring Organizations of the Treadway Commission (the COSO criteria). The Company’s management is responsible for maintaining effective internal control over financial reporting and for its assessment of the effectiveness of internal control over financial reporting.reporting, included in Item 9A, Management’s Report on Internal Control Over Financial Reporting. Our responsibility is to express an opinion on management’s assessment and an opinion on the effectiveness of the Company’s internal control over financial reporting based on our audit.
We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material respects. Our audit included obtaining an understanding of internal control over financial reporting, evaluating management’s assessment,assessing the risk that a material weakness exists, and testing and evaluating the design and operating effectiveness of internal control andbased on the assessed risk. Our audit also included performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.
A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with accounting principles generally accepted in the United States of America.accounting principles. A company’s internal control over financial reporting includes those policies and procedures that (i)(1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly reflect the transactions and dispositions of the assets of the company; (ii)(2) provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with accounting principles generally accepted in the United States of America,accounting principles, and that receipts and expenditures of the company are being made only in accordance with authorizations of management and directors of the company; and (iii)(3) provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on the financial statements.
Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.
In our opinion, management’s assessment that the Company maintained effective internal control over financial reporting as of December 31, 2006 is fairly stated, in all material respects, based on the COSO criteria Also, in our opinion, the CompanyHythiam, Inc and subsidiaries maintained, in all material respects, effective internal control over financial reporting as of December 31, 2006,2007, based on the COSO criteria.criteria.
We also have also audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the consolidated balance sheets of Hythiam, Inc. as of December 31, 20062007 and 20052006, and the related consolidated statements of operations, stockholders’ equity, and cash flows for each of the three years in the period ended December 31, 2006,2007 and our report dated March 14, 20072008 expressed an unqualified opinion on those consolidated financial statements.thereon.
/s/ BDO Seidman, LLP
Los Angeles, California
March 14, 20072008

F-3



HYTHIAM, INC. AND SUBSIDIARIES
F-3
CONSOLIDATED BALANCE SHEETS
December 31, 2006 and 2005
(In thousands, except share data)
         
  December 31, 
  2006  2005 
ASSETS
        
 
Current assets
        
Cash and cash equivalents $5,701  $3,417 
Marketable securities, at fair value  37,746   43,583 
Restricted cash  82   44 
Receivables, net  637   249 
Prepaids and other current assets  383   427 
       
Total current assets  44,549   47,720 
Long-term assets
        
Property and equipment, net  3,711   3,498 
Intellectual property, net  3,397   2,733 
Deposits and other assets  548   511 
       
Total Assets
 $52,205  $54,462 
       
         
LIABILITIES AND STOCKHOLDERS’ EQUITY
        
         
Current liabilities
        
Accounts payable $6,114  $2,652 
Accrued compensation and benefits  2,786   1,285 
Other accrued liabilities  551   364 
       
Total current liabilities  9,451   4,301 
Long-term liabilities
        
Deferred rent  498   422 
Capital lease obligations  183    
Other long-term liabilities  44    
       
Total Liabilities
  10,176   4,723 
Commitments and contingencies (note 10)        
Stockholders’ equity
        
Preferred stock, $.0001 par value; 50,000,000 shares authorized; no shares issued and outstanding      
Common stock, $.0001 par value; 200,000,000 shares authorized; 43,917,000 and 39,504,000 shares issued and 43,557,000 and 39,144,000 shares outstanding at December 31, 2006 and December 31, 2005, respectively  4   4 
Additional paid-in-capital  119,764   89,176 
Accumulated deficit  (77,739)  (39,441)
       
Total Stockholders’ Equity
  42,029   49,739 
       
Total Liabilities and Stockholders’ Equity
 $52,205  $54,462 
       
See accompanying notes to consolidated financial statements.
HYTHIAM, INC.  AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
       
(In thousands, except share data) December 31,
  2007 2006
ASSETS      
Current assets      
Cash and cash equivalents $11,149  $5,701 
Marketable securities, at fair value  35,840   37,746 
Restricted cash  39   82 
Receivables, net  1,787   637 
Notes receivable  133   - 
Prepaids and other current assets  1,394   383 
Total current assets  50,342   44,549 
         
Long-term assets        
Property and equipment, net of accumulated depreciation     
of $5,630,000 and $2,224,000, respectively  4,291   3,711 
Goodwill  10,557   - 
Intangible assets, less accumulated amortization of        
$1,609,000 and $591,000, respectively  4,836   3,397 
Deposits and other assets  620   548 
Total Assets $70,646  $52,205 
         
LIABILITIES AND STOCKHOLDERS' EQUITY        
Current liabilities        
Accounts payable $4,038  $6,114 
Accrued compensation and benefits  2,860   2,786 
Accrued liabilities  2,030   551 
Accrued claims payable  5,464   - 
Short-term debt  4,742   - 
Income taxes payable  94   - 
Total current liabilities  19,228   9,451 
         
Long-term liabilities        
Long-term debt  2,057   - 
Accrued reinsurance claims payable  2,526   - 
Warrant liability  2,798   - 
Capital lease obligations  331   183 
Deferred rent and other long-term liabilities  442   542 
Total Liabilities  27,382   10,176 
         
Commitments and contingencies (See Note 14)
        
         
Stockholders' equity        
Preferred stock, $.0001 par value; 50,000,000 shares authorized; 
no shares issued and outstanding  -   - 
Common stock, $.0001 par value; 200,000,000 shares authorized; 
54,335,000 and 43,917,000 shares issued and 54,335,000     
and 43,557,000 shares outstanding at December 31, 2007     
and December 31, 2006, respectively  5   4 
Additional paid-in-capital  166,460   119,764 
Accumulated deficit  (123,201)  (77,739)
Total Stockholders' Equity  43,264   42,029 
Total Liabilities and Stockholders' Equity $70,646  $52,205 
         
See accompanying notes to financial statements.

F-4



HYTHIAM, INC. AND SUBSIDIARIES
F-4
CONSOLIDATED STATEMENTS OF OPERATIONS
Years ended December 31, 2006, 2005 and 2004
(In thousands, except per share amounts)
             
  Year Ended December 31, 
  2006  2005  2004 
Revenues
 $3,906  $1,164  $192 
Operating expenses
            
Cost of services  818   134   17 
General and administrative expenses            
Salaries and benefits  16,212   9,204   5,117 
Other expenses  22,468   13,173   6,156 
Research and development  3,053   2,646   177 
Depreciation and amortization  1,281   879   670 
          
Total operating expenses  43,832   26,036   12,137 
Loss from operations
  (39,926)  (24,872)  (11,945)
Interest income  1,630   834   171 
          
Loss before provision for income taxes
  (38,296)  (24,038)  (11,774)
Provision for income taxes  2      1 
          
Net loss
 $(38,298) $(24,038) $(11,775)
          
             
Net loss per share — basic and diluted
 $(0.96) $(0.77) $(0.47)
          
             
Weighted average number of shares oustanding — basic and diluted
  39,715   31,173   24,877 
          
See accompanying notes to consolidated financial statements.
HYTHIAM, INC.  AND SUBSIDIARIES 
CONSOLIDATED STATEMENTS OF OPERATIONS 
          
          
(In thousands, except per share amounts) Year Ended December 31, 
  2007  2006  2005 
Revenues         
Behavioral health managed care services $36,306  $-  $- 
Healthcare services  7,695   3,906   1,164 
Total revenues  44,001   3,906   1,164 
             
Operating Expenses            
Behavioral health managed care expenses  35,679   -   - 
Cost of healthcare services  2,052   818   134 
General and administrative expenses  45,554   38,680   22,105 
Impairment loss  2,387   -   272 
Research and development  3,358   3,053   2,646 
Depreciation and amortization  2,502   1,281   879 
             
Total operating expenses  91,532   43,832   26,036 
             
Loss from operations  (47,531)  (39,926)  (24,872)
Interest income  1,584   1,630   834 
Interest expense  (2,190)  -   - 
Loss on extinguishment of debt  (741)  -   - 
Change in fair value of warrant liability  3,471   -   - 
Other non-operating income, net  32   -   - 
             
Loss before provision for income taxes  (45,375)  (38,296)  (24,038)
Provision for income taxes  87   2   - 
             
Net loss $(45,462) $(38,298) $(24,038)
             
Net loss per share - basic and diluted $(0.99) $(0.96) $(0.77)
             
Weighted average number of shares outstanding - basic and diluted  45,695   39,715   31,173 
             
See accompanying notes to financial statements. 

F-5



HYTHIAM, INC. AND SUBSIDIARIES
F-5
CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY
Years ended December 31, 2006, 2005 and 2004
                     
          Additional       
(In thousands) Common Stock  Paid-In  Accumulated    
  Shares  Amount  Capital  Deficit  Total 
Balance at December 31, 2003
  24,607  $3  $24,113  $(3,628) $20,488 
                     
Common stock, options and warrants issued for outside services  17      1,351      1,351 
Common stock issued in private placement offering, net of expenses  5,017      21,349      21,349 
Common stock issued for intellectual property acquired  83      354      354 
Exercise of warrants  27      67      67 
Net loss           (11,775)  (11,775)
                
Balance at December 31, 2004
  29,751   3   47,234   (15,403)  31,834 
                     
Common stock, options and warrants issued for outside services  23      1,501      1,501 
Exercise of options and warrants  170      265      265 
Common stock issued in public offering, net of expenses  9,200   1   40,176      40,177 
Net loss           (24,038)  (24,038)
                
Balance at December 31, 2005
  39,144   4   89,176   (39,441)  49,739 
                     
Common stock issued for intellectual property and outside services  157      1,064      1,064 
Options and warrants issued for employee and outside services        3,462      3,462 
Exercise of options and warrants  683      1,690      1,690 
Common stock issued in private placement offering, net of expenses  3,573      24,372      24,372 
Net loss           (38,298)  (38,298)
                
Balance at December 31, 2006
  43,557  $4  $119,764  $(77,739) $42,029 
                

See accompanying notes to consolidated financial statements.

F-6


HYTHIAM, INC.  AND SUBSIDIARIES 
CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY 
                
        Additional       
(In thousands) Common Stock  Paid-In  Accumulated    
  Shares  Amount  Capital  Deficit  Total 
                
Balance at December 31, 2004  29,751  $3  $47,234  $(15,403) $31,834 
                     
Common stock, options and warrants                    
issued for outside services  23   -   1,501   -   1,501 
Exercise of options and warrants  170   -   265   -   265 
Common stock issued in public                    
offering, net of expenses  9,200   1   40,176   -   40,177 
Net loss  -   -   -   (24,038)  (24,038)
Balance at December 31, 2005  39,144   4   89,176   (39,441)  49,739 
                     
Common stock issued for intellectual property                 
and outside services  157   -   1,064   -   1,064 
Options and warrants issued for                    
employee and outside services  -   -   3,462   -   3,462 
Exercise of options and warrants  683   -   1,690   -   1,690 
Common stock issued in private                    
placement offering, net of expenses  3,573   -   24,372   -   24,372 
Net loss  -   -   -   (38,298)  (38,298)
Balance at December 31, 2006  43,557   4   119,764   (77,739)  42,029 
                     
Common stock issued for intellectual property                 
and outside services  315   -   2,447   -   2,447 
Options and warrants issued for                    
employee and outside services  -   -   2,397   -   2,397 
Exercise of options and warrants  586   -   1,940   -   1,940 
Common stock issued for employee stock                    
purchase plan  27   -   124   -   124 
Common stock issued for CompCare                    
acquisition  215   -   2,084   -   2,084 
Warrants issued with debt  -   -   1,342   -   1,342 
Common stock issued in registered                    
direct placement, net of expenses  9,635   1   36,362   -   36,363 
Net loss  -   -   -   (45,462)  (45,462)
Balance at December 31, 2007  54,335  $5  $166,460  $(123,201) $43,264 
                     
See accompanying notes to consolidated financial statements. 

HYTHIAM, INC. AND SUBSIDIARIES
F-6
CONSOLIDATED STATEMENTS OF CASH FLOWS
Years ended December 31, 2006, 2005 and 2004
             
  Year ended December 31, 
  2006  2005  2004 
  (In thousands) 
Operating activities
            
Net loss $(38,298) $(24,038) $(11,775)
Adjustments to reconcile net loss to net cash used in operating activities:            
Depreciation and amortization  1,281   879   670 
Deferred rent  134   124   (17)
Provision for doubtful accounts  281   25   10 
Share-based compensation  3,691   1,701   1,172 
Lease incentives granted  68   30   301 
Asset impairment     272    
Loss on disposition of fixed assets     64    
Changes in current assets and liabilities:            
Receivables  (737)  (136)  (24)
Prepaids and other current assets  141   (181)  (20)
Accounts payable  3,462   2,043   (650)
Accrued compensation and benefits  1,501   459   508 
Other accrued liabilities  45   (31)  (122)
          
Net cash used in operating activities  (28,431)  (18,789)  (9,947)
Investing activities
            
Purchase of marketable securities  (47,813)  (80,704)  (31,914)
Proceeds from sales and maturities of marketable securities  53,650   60,600   21,631 
Restricted cash  (38)  (44)   
Purchases of property and equipment  (957)  (1,803)  (506)
Intellectual property costs  (143)  (139)  (126)
Deposits and other assets  (37)  (146)  2 
          
Net cash provided by (used in) investing activities  4,662   (22,236)  (10,913)
Financing activities
            
Net proceeds from sale of common stock  24,372   40,177   21,349 
Exercises of stock options and warrants  1,690   265   67 
Capital lease obligations  (9)      
          
Net cash provided by financing activities  26,053   40,442   21,416 
             
Net increase (decrease) in cash and cash equivalents
  2,284   (583)  556 
Cash and cash equivalents at beginning of period
  3,417   4,000   3,444 
          
Cash and cash equivalents at end of period
 $5,701  $3,417  $4,000 
          
             
Supplemental disclosure of cash paid
            
Income taxes $2  $  $2 
             
Supplemental disclosure of non-cash activity
            
Common stock issued for intellectual property $738  $  $354 
Common stock, options and warrants issued for outside services  97      199 
Property and equipment aquired through capital leases and other financing  320       

See accompanying notes to consolidated financial statements.

F-7


HYTHIAM, INC. AND SUBSIDIARIES 
CONSOLIDATED STATEMENTS OF CASH FLOWS 
          
  Year ended December 31, 
(In thousands) 2007  2006  2005 
          
Operating activities         
Net loss $(45,462) $(38,298) $(24,038)
Adjustments to reconcile net loss to net cash used in operating activities:            
Depreciation and amortization  2,500   1,281   879 
Amortization of debt discount, issuance cost included in interest expense  1,026   -   - 
Provision for doubtful accounts  528   281   25 
Deferred rent  (6)  134   124 
Share-based compensation expense  2,605   3,691   1,701 
Impairment loss  2,387   -   272 
Loss on extinguishment of debt  741   -   - 
Fair value adjustment on warrant liability  (3,471)  -   - 
Loss on disposition of fixed assets  -   -   64 
Changes in current assets and liabilities, net of business acquired:            
Receivables  (810)  (737)  (136)
Prepaids and other current assets  (529)  141   (181)
Accrued claims payable  2,865   -   - 
Accounts payable  (1,594)  5,008   2,471 
   Net cash used in operating activities  (39,220)  (28,499)  (18,819)
             
Investing activities            
Purchases of marketable securities  (80,168)  (47,813)  (80,704)
Proceeds from sales and maturities of marketable securities  82,104   53,650   60,600 
Cash paid related to acquisition of a business, net of cash acquired  (4,760)  -   - 
Restricted cash  43   (38)  (44)
Purchases of property and equipment  (1,142)  (889)  (1,773)
Deposits and other assets  152   (37)  (146)
Cost of intangibles  (320)  (143)  (139)
  Net cash (used in) provided by investing activities  (4,091)  4,730   (22,206)
             
Financing activities            
Proceeds from sale of common stock and warrants  37,512   24,372   40,177 
Cost related to issuance of common stock  (230)  -   - 
Cost related to issuance of debt and warrants  (303)  -   - 
Proceeds from issuance of debt and warrants  10,000   -   - 
Capital lease obligations  (178)  (9)  - 
Exercises of stock options and warrants  1,958   1,690   265 
  Net cash provided by financing activities  48,759   26,053   40,442 
             
Net increase in cash and cash equivalents  5,448   2,284   (583)
Cash and cash equivalents at beginning of period  5,701   3,417   4,000 
Cash and cash equivalents at end of period $11,149  $5,701  $3,417 
             
Supplemental disclosure of cash paid            
Interest $1,059  $-  $- 
Income taxes  36   2   - 
Supplemental disclosure of non-cash activity            
Common stock, options and warrants issued for outside services $232  $97  $- 
Common stock issued for intellectual property  -   738   - 
Property and equipment acquired through capital leases and other financing  284   320   - 
Common stock issued for acquisition of a business  2,084   -   - 
Stock issued for redemption of debt  5,350   -   - 


HYTHIAM, INC. AND SUBSIDIARY
Notes to Consolidated Financial Statements

Note 1.  Summary of Significant Accounting Policies

Description of Business

Hythiam, Inc. (referred to herein as the company, we, us and our) is a healthcare services management company, focused on delivering solutions for those suffering from alcoholismproviding behavioral health management services to health plans, employers, criminal justice, and other substance dependencies.government agencies through a network of licensed and company managed healthcare providers. We also research, develop, license and commercialize innovative physiological, nutritional, and behavioral treatment protocols.programs. Through our subsidiary, Comprehensive Care Corporation (CompCare), we manage all behavioral health disorders. We utilize CompCare’s infrastructure to offer our proprietary disease management services.  Our disease management offering combines medical and behavioral treatment modalities to manage substance dependent populations, and is built around our proprietary PROMETA® Treatment Programs for alcoholism and dependence to cocaine and methamphetamines. Our PROMETA treatment protocols,Treatment Programs, which integrate behavioral, nutritional, and medical components, are available through licensed treatment providers. We also license or manage treatment centers that offer the PROMETA Treatment Programs, as well as other treatments for substance dependencies.

On January 12, 2007, we acquired all of the outstanding membership interest of Woodcliff Healthcare Investment Partners, LLC (Woodcliff), which owns 1,739,130 shares of common stock and 14,400 shares of Series A Convertible Preferred Stock of CompCare. The conversion of the preferred stock would result in us owning approximately 50.05% of the outstanding shares of CompCare based on shares outstanding as of December 31, 2007. The preferred stock has voting rights and, combined with the common shares held by us, gives us voting control over CompCare. We began consolidating CompCare’s accounts on January 13, 2007. See further discussion in Note 5 — Acquisition of Woodcliff and Controlling Interest in CompCare.

CompCare manages the delivery of a continuum of psychiatric and substance abuse services to commercial, Medicare and Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators and commercial and other group purchasers of behavioral healthcare services. The customer base for CompCare’s services includes both private and governmental entities.

We currently operate in onewithin two reportable segments: healthcare services and behavioral health managed care services. Our healthcare services segment focusedfocuses on providing licensing, administrative and management services to licensees that administer PROMETA and other treatment protocols,programs, including PROMETA Centers that are licensed and/or managed by us. Substantially, alltreatment centers. Our behavioral health managed care services segment currently focuses on providing managed care services in the behavioral health, psychiatric and substance abuse fields, and principally includes the operations of our licensing and service-relatedmajority-owned, controlled subsidiary, CompCare. A majority of our consolidated revenues and assets are earned or located within the United States.

Basis of Consolidation and Presentation

Our consolidated financial statements include the accounts of the company, and our wholly-owned subsidiaries, CompCare, and the accounts of The PROMETA Center, Inc., a Californiacompany-managed professional corporation.medical corporations. Based on the provisions of a management services agreementagreements between us and the PROMETA Center,medical corporations, we have determined that the PROMETA Center is amedical corporations are variable interest entity,entities, and that we are the primary beneficiary as defined in Financial Accounting Standards Board (FASB) Interpretation No. 46R, “Consolidation of Variable Interest Entities,” an Interpretation of Accounting Research Bulletin No. 51 (FIN 46R). Accordingly, we are required to consolidate the revenues and expenses of the PROMETA Center.managed medical corporations. See further discussion below in “Variable Interest Entities” and Note 2 Management Services Agreement.

All intercompany transactions have been eliminated in consolidation. Certain amounts in the consolidated financial statements and notes thereto for the years ended December 31, 20052006 and 20042005 have been reclassified to conform to the presentation for the year ended December 31, 2006.2007.



Use of Estimates

The preparation of financial statements in conformity with generally accepted accounting principles (GAAP) in the United States of America requires management to make estimates and assumptions that affect the reported amounts in the financial statements and disclosed in the accompanying notes. Significant areas requiring the use of management estimates related to expense accruals, accounts receivable allowances, patient continuing care reserves, accrued claims payable, premium deficiencies, the useful life of depreciable assets, the evaluation of asset impairment and shared-based compensation. Actual results could differ from those estimates.

Revenue Recognition

Healthcare Services

    Our healthcare services revenues to date have been derived from licensing our treatment protocolsprograms and providing administrative services to hospitals, treatment facilities and other healthcare providers, and from patient revenues generated by the PROMETA Center.our managed treatment centers.  We determine revenues earned based on the terms of theseour licensing and management contracts, which determination requires the use of judgment, including the assessment of the collectibilitycollectability of receivables. Licensing agreements typically provide for a fixed fee on a per-patient basis, payable to us following the provider’s commencement of the patient’s initial treatment usinguse of our protocol.program to treat a patient.  For revenue recognition purposes, we treat the protocolprogram licensing and related administrative services as one unit of accounting.  We record the fees owed to us under the terms of the agreements at the time we have performed substantially all required services for each patient’s treatment,use of our program, which for the significant majority of our license agreements to date is in the period in which the patient’sprovider begins using the program for  medically directed and supervised treatment has commenced,of a patient and, in other cases, is at the time thethat medical treatment has been completed.

F-8



The revenues of the PROMETA Center,managed treatment centers, which we include in our consolidated financial statements, are derived from charging fees directly to patients for medical treatments, usingincluding the PROMETA protocols.Treatment Programs.  Revenues from patients treated at the PROMETA Center, which were approximately $1.1 million and 29% of our revenue in 2006,managed treatment centers are recorded based on the number of days of treatment completed during the period as a percentage of the total number treatment days for the protocols.PROMETA Treatment Programs.  Revenues relating to the continuing care portion of the treatmentPROMETA Treatment Programs are deferred and recorded over the period that the continuing care services are provided.

One of our managed treatment centers, the PROMETA Center, located in Santa Monica California, accounted for approximately 18% and 29% of healthcare services revenues, and 3% and 29% of consolidated revenues in 2007 and 2006, respectively. No other licensee or managed medical practice accounted for over 10% of ourhealthcare services or consolidated revenues in 2006, whereas in2007 or 2006. In 2005 three of our licensees each accounted for over 10% of ourhealthcare services revenues, representing 25%, 20% and 18% of oursuch revenues. One licensee

Behavioral Health Managed Care Services

Managed care activities are performed by CompCare under the terms of agreements with health maintenance organizations (HMOs), preferred provider organizations, and other health plans or payers to provide contracted behavioral healthcare services to subscribing participants. Revenue under a substantial portion of these agreements is earned monthly based on the number of qualified participants regardless of services actually provided (generally referred to as capitation arrangements). The information regarding qualified participants is supplied by CompCare’s clients and CompCare reviews membership eligibility records and other reported information to verify its accuracy in determining the amount of revenue to be recognized. Capitation agreements accounted for 93%$35.6 million, or 97% of ourbehavioral health managed care revenues in 2004.
Basic and Diluted Loss per Share
          Basic loss per share is computed by dividing the net loss to common stockholders for the period January 13 through December 31, 2007. The remaining balance of CompCare’s revenues is earned on a fee-for-service basis and is recognized as services are rendered.

Cost of Healthcare Services

Cost of healthcare services represent direct costs that are incurred in connection with licensing our treatment programs and providing administrative services in accordance with the various technology license and services agreements, and are associated directly with or vary directly with, the revenue that we recognize. Consistent


with our revenue recognition policy, the costs associated with providing these services are recognized, for a significant majority of our agreements, in the period in which patient treatment commences, and in other cases, at the time treatment has been completed. Such costs include royalties paid for the use of the PROMETA Treatment Program for patients treated by all licensees, and direct labor costs, continuing care expense, medical supplies and program medications for patients treated at the managed treatment centers.

Behavioral Health Managed Care Services Expense Recognition

Behavioral health managed care operating expense is recognized in the period in which an eligible member actually receives services and includes an estimate of the cost of behavioral health services that have been incurred but not yet reported (IBNR).  See “Accrued Claims Payable” for a discussion of IBNR claims. CompCare contracts with various healthcare providers including hospitals, physician groups and other licensed behavioral healthcare professionals either on a discounted fee-for-service or a per-case basis.  CompCare determines that a member has received services when CompCare receives a claim within the contracted timeframe with all required billing elements correctly completed by the weighted average numberservice provider. CompCare then determines that the member is eligible to receive such services, the service provided is medically necessary and is covered by the benefit plan’s certificate of common shares outstanding duringcoverage, and the period. Dilutedservice is authorized by one of its employees.  If all of these requirements are met, the claim is entered into CompCare’s claims system for payment.

Premium Deficiencies

CompCare accrues losses under its capitated contracts when it is probable that a loss per sharehas been incurred and the amount of the loss can be reasonably estimated. CompCare performs this loss accrual analysis on a specific contract basis taking into consideration such factors as future contractual revenue, projected future healthcare and maintenance costs, and each contract's specific terms related to future revenue increases as compared to expected increases in healthcare costs. The projected future healthcare and maintenance costs are estimated based on historical trends and CompCare’s estimate of future cost increases.

At any time prior to the end of a contract or contract renewal, if a capitated contract is computednot meeting its financial goals, CompCare generally has the ability to cancel the contract with 60 to 90 days’ written notice.  Prior to cancellation, CompCare will usually submit a request for a rate increase accompanied by dividingsupporting utilization data.  Although CompCare’s clients have historically been generally receptive to such requests, no assurance can be given that such requests will be fulfilled in the net lossfuture in CompCare’s favor.  If a rate increase is not granted, CompCare has the ability, in most cases, to terminate the contract and limit its risk to a short-term period.

On a quarterly basis, CompCare performs a review of its portfolio of contracts for the purpose of identifying loss contracts (as defined in the American Institute of Certified Public Accountants Audit and Accounting Guide – Health Care Organizations) and developing a contract loss reserve, if applicable, for succeeding periods. During the period by the weighted average number of common and dilutive common equivalent shares outstanding during the period.
          Common equivalent shares, consisting of approximately 7,222,000, 6,901,000 and 6,379,000 of incremental common shares as ofJanuary 13 through December 31, 2006, 2005 and 2004, respectively, issuable upon the exercise of stock options and warrants have been excluded2007, CompCare identified two contracts that were not meeting their financial goals. CompCare successfully obtained a rate increase from the diluted earnings per share calculation because their effectclients, effective January 1, 2008.  At December 31, 2007, CompCare believes no contract loss reserve for future periods is anti-dilutive.necessary for these contracts.

Share-Based Compensation

Under the Hythiamour 2003 and 2007 Stock Incentive PlanPlans (the Plan)Plans), we granthave granted incentive stock options (ISOs) under Section 422A of the Internal Revenue Code and non-qualified stock options (NSOs) to executive officers, employees, members of our board of directors, and certain outside consultants. We grant all such share-based compensation awards at no less than the fair market value of our stock on the date of grant. Employee and board of director awards generally vest on a straight-line basis over five and four years, respectively. Total share-based compensation expense on a consolidated basis amounted to $2.6 million, $3.7 million and $1.7 million for the years ended December 31, 2007, 2006 and 2005, respectively.



Stock Options Employees and Directors

On January 1, 2006, we adopted Statement of Financial Accounting Standards (SFAS) No. 123 (Revised 2004), “Share-Based Payment,” (SFAS 123R), which requires the measurement and recognition of compensation expense for all share-based payment awards made to employees and directors based on estimated fair values at the date of grant using an option-pricing model. SFAS 123R replaces SFAS 123, “Accounting for Stock-Based Compensation” (SFAS No. 123) for awards granted to employees and directors and supersedes Accounting Principles Board Opinion No. 25, “Accounting for Stock Issued to Employees” (APB 25). Prior to the adoption of SFAS 123R, we accounted for shared-basedshare-based payment awards to employees and directors using the intrinsic value method in accordance with APB 25 as allowed under SFAS 123. Under APB 25, we recognized no share-based compensation expense in our consolidated statements of operations for awards to employees and directors because the exercise price of our stock options equaled the fair market value of the underlying stock at the date of grant. Under the provisions of SFAS 123R, share based compensation expense is recognized over the employee’s requisite service period (generally the vesting period of the equity grant) using the straight-line method, and is reduced for estimated forfeitures. SFAS 123R requires forfeitures to be estimated at the time of grant and revised, if necessary, in subsequent periods if actual forfeitures differ from those estimates. In our pro-formapro forma information required under SFAS No. 123 for the periods prior to 2006, we accounted for forfeitures as they occurred.

We adopted SFAS 123R using the modified prospective method, and in accordance with that method, our consolidated financial statements for 2006 include compensation expense related to the unvested portion of share-based payment awards granted prior to January 1, 2006 based on the grant date fair value estimated in accordance with the pro-formapro forma provisions of SFAS 123. Prior periods have not been restated to reflect, and do not include, the impact of SFAS 123R. As a result of adopting SFAS 123R on January 1, 2006, share-based compensation expense

F-9


recognized under SFAS 123R for employees and directors for 2006 and 2007 was $2.3 million and $2.4 million, respectively, which impacted our basic and diluted loss per share by $0.06.$0.06 and $0.05, respectively.

Had we determined compensation cost based on the fair value at the grant date for such stock options under SFAS 123 for the yearsyear ended December 31, 2005, and 2004, the pro forma effect on net loss and net loss per share would have been as follows:
         
  2005  2004 
Net loss as reported $(24,038,000) $(11,775,000)
Add: Stock-based compensation expense  20,000    
Less: Stock-based expense determined under fair value based method  (901,000)  (463,000)
       
Pro forma net loss $(24,919,000) $(12,238,000)
       
         
Net loss per share:        
As reported — basic and diluted $(0.77) $(0.47)
Pro forma — basic and diluted $(0.80) $(0.49)

  2005 
Net loss as reported $(24,038,000)
Add: Stock-based compensation expense  20,000 
Less: Stock-based expense determined under    
fair value based method  (901,000)
Pro forma net loss $(24,919,000)
     
Net loss per share:    
As reported –  basic and diluted $(0.77)
Pro forma –  basic and diluted $(0.80)

The estimated weighted average fair values of options granted during 2007, 2006 and 2005 were $4.50, $3.95 and 2004 were $3.95, $4.08 and $2.60 per share, respectively, and were calculated using the Black-Scholes pricing model based on the following assumptions:
             
  2006 2005 2004
Expected volatility  66%  58%  61%
Risk-free interest rate  4.72%  4.18%  4.24%
Weighted average expected lives  6.1years  10years  10years
Expected dividend yield  0%  0%  0%

 2007 2006 2005
Expected volatility64% 66% 58%
Risk-free interest rate4.46% 4.72% 4.18%
Weighted average expected lives in years6.5 6.1 10.0
Expected dividend yield0% 0% 0%

The expected volatility assumption for 2007, 2006 and 2005 was based on the historical volatility of our stock and the stock of other public healthcare companies, measured over a period generally commensurate with the expected term. The weighted average expected option term for 2007 and 2006 reflects the application of the


simplified method set out in SEC Staff Accounting Bulletin No. 107, which defines the life as the average of the contractual term of the options and the weighted average vesting period for all option tranches.  We use historical data to estimate the rate of forfeitures assumption for awards granted to employees, which amounted to 8.8%29% in 2007 and 27% in 2006.

We have elected to adopt the detailed method prescribed in SFAS 123R for calculating the beginning balance of the additional paid-in capital pool (APIC pool) related to the tax effects of employee share-based compensation, and to determine the subsequent impact on the APIC pool and consolidated statements of cash flows of the tax effects of employee share-based compensation awards that were outstanding upon adoption of SFAS 123R.

Stock Options and Warrants Non-employees

We account for the issuance of stock options and warrants for services from non-employees in accordance with SFAS 123 by estimating the fair value of stock options and warrants issued using the Black-Scholes pricing model. This model’s calculations include the exercise price, the market price of shares on grant date, the weighted average information for risk-free interest, expected life of the option or warrant, expected volatility of our stock and expected dividends.

For options and warrants issued as compensation to non-employees for services that are fully vested and non-forfeitable at the time of issuance, the estimated value is recorded in equity and expensed when the services are performed and benefit is received as provided by FASB Emerging Issues Task Force Issue (EITF) No. 96-18, “Accounting For Equity Instruments That Are Issued To Other Than Employees For Acquiring Or In Conjunction With Selling Goods Or Services.” For unvested shares, the change in fair value during the period is recognized in expense using the graded vesting method.

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Share-based expense relating to stock options and warrants granted and common stock issued to non-employees was $1.2$104,000, $1.4 million and $1.6 million for 2007, 2006 and 2005, respectively.

Stock Options – CompCare Employees, Directors and Consultants

CompCare’s 1995 and 2002 Incentive Plans (the CompCare Plans) provide for the issuance of ISOs, NSOs, stock appreciation rights, limited stock appreciation rights, and restricted stock grants to eligible employees and consultants, and stock options to its employees and non-employee directors. Options for ISOs may be granted for terms of up to ten years and are generally exercisable in cumulative increments of 50% each six months. CompCare also has a non-qualified stock option plan for its outside directors, in which the option grants vest in accordance with vesting schedules established by CompCare’s Compensation and Stock Option Committee.

CompCare has adopted SFAS 123R, using the modified prospective method and used a Black-Scholes valuation model to determine the fair value of options on the grant date. As a result of adopting SFAS 123R, share-based compensation expense recognized for employees and directors for the period January 13 through December 31, 2007 was $83,000.



The following table lists the assumptions utilized in applying the Black-Scholes valuation model.  CompCare uses historical data to estimate the expected term of the option.  Expected volatility is based on the historical volatility of the CompCare’s traded stock.  CompCare did not declare dividends in the past nor does it expect to do so in the near future, and as such it assumes no expected dividend.  The risk-free rate is based on the U.S. Treasury yield curve with the same expected term as that of the option at the time of grant.

For the period
January 13 through 
December 31, 2007
Expected volatility110%
Risk-free interest rate4.87%
Weighted average expected lives in years3.3
Expected dividend yield0%
Advertising Costs

Costs incurred for advertising, including production costs, are generally expensed when incurred or expensed on a straight-line basis over the periods that advertisements are run.  Our advertising costs were approximately $680,000, $3.3 million and $1.1 million in 2007, 2006 and 2005, respectively.

Foreign Currency

Assets and liabilities of foreign subsidiaries are translated into U.S. dollars at year-end exchange rates.  Income and expense items are translated at average exchange rates prevailing during the year.  The local currency is the functional currency.  Foreign currency transaction gains (losses) of approximately ($22,000), $20,000 and $21,000 for the years ended December 31, 2007, 2006 and 2005, respectively, are primarily related to intercompany receivables and 2004, respectively.payables for which settlement is planned in the foreseeable future, and are included in the consolidated statements of operations.  There were no foreign currency translation adjustments recorded to other comprehensive income.

Income Taxes

We account for income taxes using the liability method in accordance with SFAS 109, "Accounting for Income Taxes." To date, no current income tax liability has been recorded due to our accumulated net losses. Deferred tax assets and liabilities are recognized for temporary differences between the financial statement carrying amount of assets and liabilities and the amounts that are reported in the tax return. Deferred tax assets and liabilities are recorded on a net basis; however, our net deferred tax assets have been fully reserved by a valuation allowance due to the uncertainty of our ability to realize future taxable income and to recover our net deferred tax assets.

In June 2006, the FASB issued Interpretation No. 48 (FIN 48), “Accounting for Uncertainty in Income Taxes,” which clarifies the accounting for uncertainty in income taxes. FIN 48 requires that companies recognize in the consolidated financial statements the impact of a tax position, if that position is more likely than not of being sustained on audit, based on the technical merits of the position. FIN 48 also provides guidance on derecognition, classification, interest and penalties, accounting in interim periods and disclosure. The provisions of FIN 48 are effective for fiscal years beginning after December 15, 2006. We adopted FIN 48 on January 1, 2007, with no impact to our consolidated financial statements.

Comprehensive Income

Comprehensive income generally represents all changes in stockholders’ equity (deficit) during the period except those resulting from investments by, or distributions to, stockholders. We have no other comprehensive income or loss items and accordingly, our net loss equals comprehensive loss.



Basic and Diluted Loss per Share

Basic loss per share is computed by dividing the net loss to common stockholders for the period by the weighted average number of common shares outstanding during the period. Diluted loss per share is computed by dividing the net loss for the period by the weighted average number of common and dilutive common equivalent shares outstanding during the period.

Common equivalent shares, consisting of approximately 9,846,000, 7,222,000, and 6,901,000 of incremental common shares as of December 31, 2007, 2006 and 2005, respectively, issuable upon the exercise of stock options and warrants have been excluded from the diluted earnings per share calculation because their effect is anti-dilutive.

Cash and Cash Equivalents

We invest available cash in short-term commercial paper, certificates of deposit and high grade variable rate securities.  Liquid investments with an original maturity of three months or less when purchased are considered to be cash equivalents.

Restricted cash represents deposits secured as collateral for a bank credit card program.

Marketable Securities

Investments includinginclude auction rate securities, commercial paper and certificates of deposit with maturity dates greater than three months when purchased, and which have readily determined fair values, which are classified as available-for-sale investments and reflected in current assets as marketable securities at fair market value. Auction rate securities are recorded at cost, which equals fair market value, as the rate on such securities generally resets every 7, 28 or 35 days. Our marketable securities at December 31 consisted of the following investments with the following maturities:
                     
  Fair Market  Less than      5-10  More than 
  Value  1 Year  1-5 Years  Years  10 Years 
December 31, 2006
                    
Variable auction rate taxable municipal securities $37,412,000  $  $  $  $37,412,000 
Certificates of deposits  334,000   334,000             
                
  $37,746,000  $334,000  $  $  $37,412,000 
                
                     
December 31, 2005
                    
Variable auction rate taxable municipal securities $43,241,000  $  $  $  $43,241,000 
Certificates of deposits  342,000   342,000          
                
  $43,583,000  $342,000  $  $  $43,241,000 
                

 Fair Market Value 
Less than
1 Year
 1-5 Years 5-10 Years 
More than 
10 Years
 
December 31, 2007          
           
Variable auction rate securities$19,000,000 $- $- $- $19,000,000 
Commercial paper 16,518,000  -  -  -  16,518,000 
Certificates of deposits 322,000  322,000  -  -  - 
 $35,840,000 $322,000 $- $- $35,518,000 
December 31, 2006               
                
Variable auction rate securities$27,464,000 $- $- $- $27,464,000 
Commercial paper 9,948,000  -  -  -  9,948,000 
Certificates of deposits 334,000  334,000  -  -  - 
 $37,746,000 $334,000 $- $- $37,412,000 
                
Auction rate securities are variable rate debt instruments with longer stated maturities whose interest rates are reset at predetermined short-term intervals through a Dutch auction system. Through February 13, 2008, all of our auction rate securities held at December 31, 2007 had completed at least one auction successfully through the normal auction process, and we had reduced our total investments in auction rate securities to $11.5 million. However, from February 14 through March 12, 2008, auctions for these securities had failed, meaning the parties desiring to sell securities could not be matched with an adequate number of buyers, resulting in our having to continue to hold these securities. Although the securities are Aaa/AAA rated and collateralized by portfolios of student loans guaranteed by the U.S. government, based on current market conditions it is likely that auctions will continue to be unsuccessful, limiting the short-term liquidity of these investments until the auction succeeds, the issuer calls the securities, or they mature.  As a result, our ability to liquidate our investment and fully recover the carrying value of our investment in the near term may be limited or not exist. If the issuers are unable to successfully close future auctions or their credit ratings deteriorate, we may in the future record an impairment charge on these


investments. In addition, these types of developments could cause us to reclassify our investments in auction rate securities from a current asset to a long-term asset.  We believe that the higher reset rates on failed auctions provide sufficient incentive for the security issuers to address this lack of liquidity. While these failures in the auction process have affected our ability to access these funds in the near term, we do not believe that the underlying securities or collateral have been affected.  At this time, we have not obtained sufficient evidence to conclude that these investments are impaired or that they will not be settled in the short term, although the market for these investments is uncertain. We believe that we will not require access to these funds in the near-term prior to restoration of liquidity in this market. These securities will be analyzed each reporting period for other-than-temporary impairment factors. If the credit rating of the security issuers deteriorates, we may be required to adjust the carrying value of these investments through an impairment charge.

The cost of theall securities presented above securities approximated fair market value at December 31.

Fair Value of Financial Instruments and Concentration of Credit Risk

FASB Statement No. 107, “Disclosures about Fair Value of Financial Instruments” requires disclosure of fair value information about financial instruments for which it is practical to estimate that value. The carrying amounts reported in the balance sheet for cash, cash equivalents, marketable securities, accounts receivable, accounts payable and accrued liabilities approximate fair value because of the immediate or short-term maturity of these financial instruments. At December 31, 2006,2007, all of our cash equivalents and marketable securities were invested in highly liquid, high grade auction rate securities, commercial paper and certificates of deposit. At December 31, 2006,2007, no single investment represented more than 6%7% of theour investment portfolio. For debt outstanding, the fair value at December 31, 2007 is estimated at $4.4 million, based on discounted cash flow calculations using the Company’s estimated incremental borrowing rate.

Property and Equipment

Property and equipment are stated at cost, less accumulated depreciation. Additions and improvements to property and equipment are capitalized at cost. Expenditures for maintenance and repairs are charged to expense as incurred. Depreciation is computed using the straight-line method over the estimated useful lives of the related assets, which range from two to seven years for furniture and equipment. Leasehold improvements are amortized over the lesser of the estimated useful lives of the assets or the related lease term, principally five to seven years.

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Variable Interest Entities

An entity is subject to FIN 46R and is called a Variable Interest Entity (VIE) if it has (a) equity that is insufficient to permit the entity to finance its activities without additional subordinated financial support from other parties, or (b) equity investors that cannot make significant decisions about the entity’s operations, or that do not absorb the expected losses or receive the expected returns of the entity. A VIE is consolidated by its primary beneficiary, which is the party that has a majority of the expected losses, or a majority of the expected residual returns of the VIE, or both. As discussed in Note 2 Management Services Agreement,Agreements, we have a management services agreementagreements with the PROMETA Center,managed medical corporations, in which we agree to provide and perform all non-medical management and administrative services for the respective medical group. We also agreed to provide a working capital loan to the PROMETA Center up to a maximum of $2.5 millionloans to allow for the medical group to pay for its obligations. Payment of our management fee is subordinate to payments of the obligations of the medical group, and repayment of the working capital loan is not guaranteed by the shareholder or other third party. Based on the provisions of these agreements, we have determined that the PROMETA Center is a VIE,managed medical corporations are VIEs, and that we are the primary beneficiary as defined in FIN 46R. Accordingly, we are required to consolidate the revenues and expenses of the managed medical corporations.

Goodwill

In accordance with SFAS 141, “Business Combinations,” the purchase price for the CompCare acquisition was allocated to the fair values of the assets acquired, including identifiable intangible assets, in accordance with our proportionate share of ownership interest, and the excess amount of purchase price over the fair values of net assets acquired resulted in goodwill that will not be deductible for tax purposes. In December 2007, we recorded a $192,000 adjustment to reduce the balance of goodwill for the favorable resolution of assumed, pre-acquisition


liabilities.  The balance of goodwill at December 31, 2007 also reflects a $98,000 reduction related to a change in minority shareholders’ interests.  As discussed in Note 5 — Acquisition of Woodcliff and Controlling Interest in CompCare, we believe our association with CompCare creates synergies to facilitate the use of PROMETA Center.
Intellectual PropertyTreatment Programs by managed care treatment providers and to provide access to an infrastructure for our planned disease management product offerings. Accordingly, the resulting goodwill has been assigned to our healthcare services reporting unit. In accordance with SFAS 142 “Goodwill and Other IntangiblesIntangible Assets,” goodwill is not amortized, but instead is subject to impairment tests. The change in the carrying amount of goodwill by reporting unit is as follows:
 
  Healthcare Services  Behavioral Health Managed Care  Total 
Balance as of January 1, 2007 $-  $-  $- 
Goodwill - CompCare acquisition  10,064,000   493,000   10,557,000 
Balance as of December 31, 2007 $10,064,000  $493,000  $10,557,000 
             

Intangible Assets

Intellectual Property

Intellectual property consists primarily of the costs associated with acquiring certain technology, patents, patents pending, know-how and related intangible assets with respect to protocolsprograms for treatment of dependence to alcohol, cocaine, methamphetamine, and other addictive stimulants. These assets are stated at cost and are being amortized on a straight-line basis, since the pattern in which the economic benefits of the intangible assets are realized cannot be precisely determined, over the remaining life of the respective patents, or patent applications, which range from twelve to twenty years.

Other Intangible Assets

Other intangible assets consist primarily of identified intangible assets acquired as part of the CompCare acquisition, representing the value of managed care contracts and marketing-related assets associated with its managed care business including the value of the healthcare provider network and the professional designation from the National Council on Quality Association (NCQA). Such assets are being amortized on a straight-line basis over their estimated remaining lives, which approximate the rate at which we believe the economic benefits of these assets will be realized.

Impairment of Long-Lived Assets

In accordance with SFAS No. 144, “Accounting for the Impairment or Disposal of Long-Lived Assets,” long-lived assets such as property, equipment and intellectual propertyintangible assets subject to amortization are reviewed for impairment whenever events or circumstances indicate that the carrying amount of these assets may not be recoverable.  In reviewing for impairment, we compare the carrying value of such assets to the estimated undiscounted future cash flows expected from the use of the assets and their eventual disposition.  When the estimated undiscounted future cash flows are less than their carrying amount, an impairment loss is recognized equal to the difference between the assets’ fair value and their carrying value.  In December 2005, we recorded an impairment charge of $272,000 in other expense to write off the capitalized costs of intellectual property relating to an acquired patent for a treatment method for opiate addiction that we have determined would not likely be utilized in our current business plan. In August 2007, we recorded an additional impairment charge of $2.4 million when we recognized the fair value of 310,000 shares of our common stock that had been previously issued as additional consideration related to the purchase of the patent. The shares had been subject to a stock pledge agreement pending the resolution of certain contingencies until we agreed to release the shares as a result of a settlement agreement reached in August 2007 with the seller of the opiate patent. The fair value of these shares was based on the closing stock price on the date of the settlement. No impairment wasother impairments were identified in our reviewreviews at December 31, 2007 and 2006.



Accrued Claims Payable

The accrued claims payable liability represents the estimated ultimate net amounts owed for all behavioral healthcare services provided through the respective balance sheet dates, including estimated amounts for claims incurred but not yet reported (IBNR) to CompCare.  The unpaid claims liability is estimated using an actuarial paid completion factor methodology and other statistical analyses and is continually reviewed and adjusted, if necessary, to reflect any change in the estimated liability. These estimates are subject to the effects of trends in utilization and other factors.  However, actual claims incurred could differ from the estimated accrued claims payable amount reported. Although considerable variability is inherent in such estimates, CompCare management believes that the unpaid claims liability is adequate.

Accrued Reinsurance Claims Payable

The accrued reinsurance claims payable liability represents amounts payable to providers under a state reinsurance program associated with CompCare’s contract to provide behavioral healthcare services to members of a Connecticut HMO. CompCare’s contract with the HMO ended December 31, 2005. At December 31, 2007, $2.5 million of reinsurance claims payable remains and is attributable to providers having submitted claims for authorized services having incorrect service codes or otherwise incorrect information that has caused payment to be denied by CompCare.  In such cases, there are statutory provisions that allow the provider to appeal a denied claim.  If no appeal is received by CompCare within the prescribed amount of time, it is probable that CompCare will be required to remit the reinsurance funds back to the appropriate party.

Capital Leases

Assets held under capital leases include furniture and computer equipment, and are recorded at the lower of the net present value of the minimum lease payments or the fair value of the leased asset at the inception of the lease. Depreciation expense is computed using the straight-line method over the estimated useful lives of the assets.  All lease agreements contain bargain purchase options at termination of the lease.
Cost
Minority Interest

Minority interest represents the minority stockholders’ proportionate share of Services
     Costthe equity of services represent direct costsCompCare. As discussed in Note 5, we acquired a majority controlling interest in CompCare as part of our Woodcliff acquisition, and we have the ability to control 50.05% of CompCare’s common stock as of December 31, 2007 from our ownership of 1,739,130 shares of common stock and 14,400 shares of CompCare’s Series A Convertible Preferred Stock (assuming conversion). Our ownership percentage as of December 31, 2007 has decreased from the 50.25% as of the date of our acquisition due to additional common stock issued by CompCare during the period. Our controlling interest requires that are incurredCompCare’s operations be included in connection with licensing our treatment protocols and providing administrative services in accordanceconsolidated financial statements, with the various technology license and services agreements, and are associated directly with or vary directly with,remaining 49.95% being attributed to minority stockholder interest. Due to CompCare’s accumulated deficit on the revenue that we recognize. Consistent with our revenue recognition policy, the costs associated with providing these services are recognized, for a significant majoritydate of our agreements,acquisition, a deficit minority stockholders’ balance in the period in which patient treatment commences, and in other cases,amount of $544,000 existed at the time treatment has been completed. Such costs include royalties paid for the use of the PROMETA treatment protocol for patients treated by licensees and the PROMETA Center, and labor costs, continuing care expense, medical supplies and protocol medications for patients treatedacquisition which was valued at the PROMETA Center.

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Advertising Costs
     Costs incurred for advertising, including production costs, are generally expensed when incurred or expensed on a straight-line basis over the periods that advertisements are run. Our advertising costs were approximately $3.3 million and $1.1 millionzero, resulting in 2006 and 2005, respectively. We had no direct advertising costs in 2004.
Foreign Currency
     Assets and liabilities of foreign subsidiaries are translated into U.S. dollars at year-end exchange rates. Income and expense items are translated at average exchange rates prevailing during the year. The local currency is the functional currency. Foreign currency transaction gains of approximately $20,000 and $21,000 for the years ended December 31, 2006 and 2005, respectively, are primarily related to intercompany receivables and payables for which settlement is plannedan increase in the foreseeable future, and are includedamount of goodwill recognized in the consolidated statements of operations. There were no foreign currency transaction gains oracquisition. The minority stockholders’ interest in any further net losses in 2004. There were no foreign currency translation adjustments recorded to other comprehensive income.
Income Taxes
     We account for income taxes using the liability method in accordance with SFAS No. 109, “Accounting for Income Taxes” (SFAS 109). To date, no current income tax liability has beenwill not be recorded due to ourthe accumulated deficit. The unrecorded minority stockholders’ interest in net losses. Deferred tax assets and liabilities are recognized for temporary differences between the financial statement carrying amount of assets and liabilities and the amounts that are reported in the tax return. Deferred tax assets and liabilities are recorded on a net basis; however, our net deferred tax assets have been fully reserved by a valuation allowance dueloss amounted to the uncertainty of our ability to realize future taxable income and to recover our net deferred tax assets.
Comprehensive Income
  Comprehensive income generally represents all changes in stockholders’ equity (deficit)$1.6 million during the period except those resulting from investments by, or distributionsJanuary 13 through December 31, 2007. The minority stockholders’ interest in any future net income will first be credited to stockholders. We have no other comprehensive income or loss itemsgoodwill to the extent of the original deficit interest, and accordingly, our net losswill not be recognized in the financial statements until the aggregate amount of such profits equals comprehensive loss.the aggregate amount of unrecognized losses.

Recent Accounting Pronouncements
     In May 2005, the FASB issued SFAS No. 154, “Accounting Changes and Error Corrections” (SFAS 154) which replaces APB Opinion No. 20, “Accounting Changes,” and FASB Statement No. 3, “Reporting Accounting Changes in Interim Financial Statements.” SFAS 154 changes the accounting for, and the reporting of, a change in accounting principle. The statement also defines and requires retrospective application of a change in accounting principle to prior periods’ financial statements unless impracticable. If retrospective application is impracticable, the new accounting principle must be applied to the asset and liability balances as of the beginning of the earliest period practicable and a corresponding adjustment to the opening balance of retained earnings for the same period, rather than being reported in the income statement. Additionally, SFAS 154 addresses a change in accounting for estimates affected by a change in accounting principle and redefines restatement as a revision to reflect the correction of an error. Our adoption of SFAS 154 on January 1, 2006 did not have a material effect on our consolidated financial statements.
     In June 2006, the FASB issued FASB Interpretation No. 48, “Accounting for Uncertainty in Income Taxes,” (FIN 48) which clarifies the accounting for uncertainty in income taxes. FIN 48 requires that companies recognize in the consolidated financial statements the impact of a tax position, if that position is more likely than not of being sustained on audit, based on the technical merits of the position. FIN 48 also provides guidance on derecognition, classification, interest and penalties, accounting in interim periods and disclosure. The provisions of FIN 48 are effective for fiscal years beginning after December 15, 2006. We will adopt FIN 48 effective January 1, 2007. We are currently evaluating the effect of this new pronouncement.

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     In September 2006, the SEC issued Staff Accounting Bulletin No. 108, “Topic 1N — Considering the Effects of Prior Year Misstatements when Quantifying Misstatements in Current Year Financial Statements,” (SAB 108) which provides guidance on quantifying prior year errors for the purpose of evaluating materiality on current year financial statements. SAB 108 is effective for fiscal years ending after November 15, 2006. We adopted this statement in the fourth quarter of 2006 without a material impact to our consolidated financial statements.
In September 2006, the FASB issued SFAS No. 157, “Fair Value Measurements,” (SFAS 157) which defines fair value, establishes a framework for measuring fair value in generally accepted accounting principles, and expands disclosures about fair value measurements. The statement is effective for financial statements issued for fiscal years beginning after November 15, 2007, and interim periods within those fiscal years. We are currently evaluating the statement to determine what, if any, impact it will have on our consolidated financial statements. The adoption of SFAS 157 is not expected to have a material impact on our financial position, results of operations or cash flows.



In November 2006,February 2007, the FASB issued Staff PositionSFAS No. EITF 00-19-2, “Accounting159, "The Fair Value Option for Registration Payment Arrangements”, which specifiesFinancial Assets and Financial Liabilities" ("SFAS 159"). SFAS 159 allows companies to measure many financial assets and liabilities at fair value. It also establishes presentation and disclosure requirements designed to facilitate comparisons between companies that the contingent obligation to make future payments or otherwise transfer consideration under a registration payment arrangement, whether issued as a separate agreement or included as a provisionchoose different measurement attributes for similar types of a financial instrument or other agreement, should be separately recognizedassets and measured. Additionally, this guidance further clarifies that a financial instrument subject to a registration payment arrangement should be accounted for in accordance with other applicable GAAP without regard to the contingent obligation to transfer consideration pursuant to the registration payment arrangement. This guidanceliabilities. SFAS 159 is effective for financial statements issued for fiscal years beginning after DecemberNovember 15, 2006,2007 and interim periods within those fiscal years. We have chosen an earlyThe adoption of this guidance effective for the fourth quarter of 2006 without a material impact to our consolidated financial statements.
     In February 2007, the FASB issued StatementSFAS No. 159 “The Fair Value Option for Financial Assets and Financial Liabilities” (SFAS 159). SFAS 159 provides that companies may elect to measure specified financial instruments and warranty and insurance contracts at fair value on a contract-by-contract basis, with changes in fair value recognized in earnings each reporting period. The election, called the “fair value option,” will enable some companies to reduce the variability in reported earnings caused by measuring related assets and liabilities differently. Companies may elect fair-value measurement when an eligible asset or liability is initially recognized or when an event, such as a business combination, triggers a new basis of accounting for that asset or liability. The election is irrevocable for every contract chosen to be measured at fair value and must be applied to an entire contract, not to only specified risks, specific cash flows, or portions of that contract. SFAS 159 is effective as of the beginning of a company’s first fiscal year that begins after November 15, 2007. Retrospective application is not allowed. Companies may adopt SFAS 159 as of the beginning of a fiscal year that begins on or before November 15, 2007 if the choiceexpected to adopt early is made after SFAS 159 has been issued and within 120 days of the beginning of the fiscal year of adoption and the entity has not issued GAAP financial statements for any interim period of the fiscal year that includes the early adoption date. Companies are permitted to elect fair-value measurement for any eligible item within SFAS 159’s scope at the date they initially adopt SFAS 159. The adjustment to reflect the difference between the fair value and the current carrying amount of the assets and liabilities for which a company elects fair-value measurement is reported as a cumulative-effect adjustment to the opening balance of retained earnings upon adoption. Companies that adopt SFAS 159 early must also adopt all of SFAS 157’s requirements at the early adoption date. We are assessing the impact of adopting SFAS 159 and currently do not believe the adoption will have a material impact on our financial position, results of operations or cash flows.

In December 2007, the FASB issued SFAS No. 141(R), "Business Combinations" ("SFAS 141(R)"). SFAS 141(R) replaces SFAS No. 141, "Business Combinations", but retains the requirement that the purchase method of accounting for acquisitions be used for all business combinations. SFAS 141(R) expands on the disclosures previously required by SFAS 141, better defines the acquirer and the acquisition date in a business combination, and establishes principles for recognizing and measuring the assets acquired (including goodwill), the liabilities assumed and any non-controlling interests in the acquired business. SFAS 141(R) also requires an acquirer to record an adjustment to income tax expense for changes in valuation allowances or uncertain tax positions related to acquired businesses. SFAS 141(R) is effective for all business combinations with an acquisition date in the first annual period following December 15, 2008; early adoption is not permitted. We will adopt this statement as of January 1, 2009. The impact SFAS 141(R) will have on our consolidated financial statements.statements will depend on the nature and size of acquisitions we complete after we adopt SFAS 141(R).

In December 2007, the FASB issued SFAS No. 160, "Noncontrolling Interests in Consolidated Financial Statements—an amendment of ARB No. 51" (SFAS 160). SFAS 160 requires that non-controlling (or minority) interests in subsidiaries be reported in the equity section of the company's balance sheet, rather than in a mezzanine section of the balance sheet between liabilities and equity. SFAS 160 also changes the manner in which the net income of the subsidiary is reported and disclosed in the controlling company's income statement. SFAS 160 also establishes guidelines for accounting for changes in ownership percentages and for deconsolidation. SFAS 160 is effective for financial statements for fiscal years beginning on or after December 1, 2008 and interim periods within those years. The adoption of SFAS 160 is not expected to have a material impact on our financial position, results of operations or cash flows.

Note 2.  Management Services AgreementAgreements
     In November 2005, we
We have executed a management services agreementagreements with David E. Smith, M.D. Medical Group, Inc., a Californiamedical professional corporation, d.b.a. The PROMETA Center, Inc. The term of the agreement was initially forcorporations and related treatment centers, with terms generally ranging from one year, and it is continuingto ten years, with provisions to continue on a month-to-month basis thereafter,following the initial term, unless terminated for cause.
     We licensed
Under each of these management services agreements we generally license to the medical group or treatment center the right to use our proprietary treatment protocolsprograms and related trademarks and agreed to provide the medical group all required day-to-day business management services, including general administrative support services, information systems, recordkeeping, scheduling, billing, collection, marketing and local business development, and assistance in obtaining and maintaining all federal, state and local licenses, certifications and regulatory permits required for, or in connection with, the medical group’s operation and equipment located at any of its offices. The medical group or treatment facility retains the sole right and obligation to provide medical services to its patients.patients and to make other medically related decisions such as the choice of medical professionals to hire or medical equipment to acquire and the ordering of drugs.

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     WeIn addition, we provide medical office space to theeach medical group located in Santa Monica, California, and, effective November 15, 2006, in San Francisco, California on a non-exclusive basis, and we are responsible for all costs associated with rent and utilities. The medical group pays us a monthly fee equal to the aggregate amount of (a) our costs of providing management services (including reasonable overhead allocable to the delivery of our services and including start-up costs such as pre-operating salaries, rent, equipment, and tenant improvements incurred for the benefit of the medical group, provided that any capitalized costs, including all start-up expense, will be amortized over a five year period), (b) 10%-15% of the foregoing costs, and (c) any performance bonus amount, as determined by the medical group in its sole discretion. The medical group’s payment of our fee is subordinate to payment of the medical group’sgroup's obligations, including physician fees and medical group employee compensation.



We have also agreed to provide a credit facility to the PROMETA Centereach medical practice to be available as a working capital loan, up to a maximum of $2,500,000 (as amended in November 2006), with interest at the Prime Rate plus 2%, to allow for the medical group to pay for its obligations, pursuant to a revolving credit note. Funds are advanced pursuant to the terms of the management services agreement described above. The note isnotes are due on demand, or upon termination of the respective management services agreement.

Based on the provisions of these agreements, we have determined that the PROMETA Center is a VIE,managed medical corporations are VIEs, and that we are the primary beneficiary as defined in FIN 46R. Accordingly, we are required to consolidate the revenues and expenses of the PROMETA Centermanaged treatment centers as discussed in Note 1 Summary of Significant Accounting Policies under “Variable Interest Entities.”

Note 3.  Receivables

Receivables consisted of the following as of December 31:31.
         
  2006  2005 
License fees receivable $659,000  $168,000 
Patient fees receivable  49,000    
Tenant improvement allowance (1)  224,000   68,000 
Other receivables  5,000   32,000 
       
Total Receivables
  937,000   268,000 
Less-allowance for doubtful accounts  (300,000)  (19,000)
       
Total Receivables, net
 $637,000  $249,000 
       
(1)Amounts receivable from landlord upon completion of lease build-out of new office space.
  2007  2006 
 License fees receivable $2,100,000  $659,000 
 Patient fees receivable  282,000   49,000 
 Tenant improvement allowance (1)  -   224,000 
 Managed care contracts  35,000   - 
 Other  21,000   5,000 
     Total Receivables  2,438,000   937,000 
 Less-allowance for doubtful accounts  (651,000)  (300,000)
     Total Receivables, net $1,787,000  $637,000 

(1) Amounts receivable from landlord upon completion of lease build-out of new office space.

We use the specific identification method for recording the provision for doubtful accounts, which was $528,000, $281,000 $25,000 and $10,000$25,000 for the years ended December 31, 2007, 2006 2005 and 2004,2005, respectively.  Accounts written off against the allowance for doubtful accounts totaled $16,000$177,000 and $11,000$16,000 for the years ended December 31, 20052007 and 2004,2005, respectively. There were no accounts written off against the allowance for doubtful accounts during the year ended December 31, 2006.

Note 4.  Property and Equipment

Depreciation and amortization of property and equipment are provided using the straight-line method over two to seven years.  Leasehold improvements are amortized over the term of the lease.  Construction in progress is not depreciated until the related asset is completed and placed into service.

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Property and equipment consisted of the following as of December 31:
         
  2006  2005 
Furniture and equipment $2,968,000  $2,154,000 
Leasehold improvements  2,967,000   2,516,000 
       
Total Cost
  5,935,000   4,670,000 
Less-accumulated depreciation  (2,224,000)  (1,172,000)
       
Property and Equipment, net
 $3,711,000  $3,498,000 
       
  2007  2006 
Furniture and equipment $6,363,000  $2,968,000 
Leasehold improvements  3,558,000   2,967,000 
    Total Cost  9,921,000   5,935,000 
Less-accumulated depreciation  (5,630,000)  (2,224,000)
    Property and Equipment, net $4,291,000  $3,711,000 

Depreciation expense was $1.5 million, $1.1 million $665,000 and $499,000$665,000 for the years ended December 31, 2007, 2006 2005 and 2004,2005, respectively.



Note 5.  Intellectual PropertyAcquisition of Woodcliff and Controlling Interest in CompCare

On January 12, 2007, we acquired all of the outstanding membership interests of Woodcliff in exchange for $9 million in cash and 215,053 shares of our common stock. The purchase price was equal to $667.27 per share of preferred stock and $0.80 per share of common stock of CompCare owned by Woodcliff. Woodcliff had no other assets or liabilities at the date of the acquisition. Woodcliff owns 1,739,130 shares of common stock and 14,400 shares of Series A Convertible Preferred Stock of CompCare, the conversion of which would result in us owning approximately 50.25% and 50.05% of the outstanding shares of common stock of CompCare based on shares outstanding at January 12, 2007 and December 31, 2007, respectively. The preferred stock has voting rights and, combined with the common shares held by us, gives us voting control over CompCare. We have anti-dilution protection and the right to designate a majority of the board of directors of CompCare. In addition, CompCare is required to obtain our consent for a sale or merger involving a material portion of CompCare's assets or business, and prior to entering into any single or series of related transactions exceeding $500,000 or incurring any debt in excess of $200,000. The acquisition was accounted for as a purchase, and we began consolidating CompCare’s results of operations on January 13, 2007. The remaining ownership interest in CompCare is being accounted for as minority interest.

CompCare provides managed care services in the behavioral health and psychiatric fields. CompCare manages the delivery of a continuum of psychiatric and substance abuse services to commercial, Medicare and Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators, and commercial and other group purchasers of behavioral healthcare services. The customer base for CompCare’s services includes both private and governmental entities. CompCare’s services are provided primarily by unrelated vendors on a subcontract basis. Since February 2006, we have had a marketing agreement with CompCare under which CompCare has the right to offer our PROMETA Treatment Programs as part of a disease management offering to its customers and other mutually agreed parties on an exclusive basis. We believe our association with CompCare creates synergies to facilitate the use of PROMETA Treatment Programs by managed care treatment providers and to provide access to an infrastructure for our disease management product offerings.

In accordance with SFAS 141, the Woodcliff purchase price was allocated to the fair value of CompCare’s assets and liabilities, including identifiable intangible assets, in accordance with our proportionate share of ownership interest, and the excess of purchase price over the fair value of net assets acquired resulted in goodwill. Goodwill related to this acquisition is not deductible for tax purposes. In accordance with SFAS 142, goodwill is not amortized, but instead is subject to impairment tests. Identified intangibles with definite useful lives are amortized on a straight-line basis over their estimated remaining lives (see Note 1 – Summary of Significant Accounting Policies, under “Goodwill”).

The primary source of funds for the Woodcliff acquisition was a $10 million senior secured note and warrant sold and issued to Highbridge International LLC (see Note 7 – Debt Outstanding).



The following table presents the allocation of the total acquisition cost, which includes the purchase price and related acquisition expenses, to the assets acquired and liabilities assumed:

  At January 12, 2007
Cash and cash equivalents $4,304,000
Other current assets  1,840,000
Property and equipment  389,000
Goodwill  10,847,000
Intangible assets  2,136,000
Other non-current assets  237,000
Total assets $19,753,000
    
Accounts payable and accrued liabilities $(1,285,000
Accrued claims payable  (2,599,000
Accrued reinsurance claims payable  (2,526,000
Long-term debt  (1,978,000
Other liabilities  (217,000
Total liabilities $(8,605,000
    
Total acquisition cost $11,148,000
    

    The allocation of the total acquisition cost is based primarily on a valuation analysis of identifiable intangible assets completed by an independent valuation specialist, Actuarial Risk Management, on July 19, 2007. In December 2007, we recorded a $192,000 adjustment to reduce the balance of goodwill for the favorable resolution of assumed, pre-acquisition liabilities. The balance of goodwill at December 31, 2007 amounted to $10.6 million, which also reflects a $98,000 reduction related to a change in minority shareholders’ interests. As discussed in Note 1, goodwill was assigned to our healthcare services reportable segment and the remaining net assets and intangible assets acquired were assigned to our behavioral health managed care reportable segment.

Assuming the acquisition had occurred January 1, 2006 pro forma revenues, net loss and net loss per share would have been $45.1 million, $45.7 million, and $1.00 for the year ended December 31, 2007, and $22.9 million, $42.3 million and $1.06 for the year ended December 31, 2006, respectively. This unaudited pro forma information does not purport to represent what our actual results of operations would have been if the acquisition had occurred as of the dates indicated or what results would be for any future periods.

Note 6.  Intangible Assets

Intangible assets consist of intellectual property and intangible assets associated with the CompCare acquisition. Intellectual property consists primarily of the costs associated with acquiring certain technology, patents, patents pending, know-how and related intangible assets with respect to protocolsprograms for treatment of dependence to alcohol, cocaine, methamphetamine, and other addictive stimulants. TheIntangible assets are stated at cost, net of accumulated amortization and areamortization. Intellectual property is being amortized on a straight-line basis from the date costs are incurred over the remaining life of the respective patents or patent applications, which range from twelve to twenty years, and other intangible assets are being amortized on a straight-line basis from the date of the acquisition over the remaining life of the managed care contracts to which they relate, which range from two to seven years. The total cost of intellectual property assets, before accumulated amortization, was $3,988,000 and $3,107,000 asAs of December 31, 2007 and 2006, the gross and 2005, respectively.net carrying amounts of intangible assets that are subject to amortization are as follows:
PROMETA Protocols

 
  2007  2006 
Amortization Period 
(in years)
Intellectual property (IP) $4,308,000  $3,988,000 12 to 20
Managed care contracts (Note 5)  832,000   - 3 to 7
Provider networks, NCQA (Note 5)  1,305,000   - 2 to 3
Total Cost  6,445,000   3,988,000  
Less-Accumulated amort-IP  (832,000)  (591,000) 
Less-Accumulated amort-Other  (777,000)  -  
  $4,836,000  $3,397,000  

PROMETA Treatment Programs

In March 2003, we entered into a Technology Purchase and License Agreement (Technology Agreement) with Tratamientos Avanzados de la Adicción S.L. (Tavad), a Spanish corporation, (Tavad), to acquire, on an exclusive basis, all of the rights, title and interest to use and or sell the products and services and license the intellectual property owned by Tavad with respect to a method for the treatment of alcohol and cocaine dependence, known as the PROMETA protocols,Treatment Programs, on a worldwide basis except in Spain (as amended in September 2003). We have granted Tavad a security interest in the intellectual property to secure the payments and performance obligations under the Technology Agreement. As consideration for the intellectual property acquired, we issued to Tavad approximately 836,000 shares of our common stock in September 2003 at a fair market value of $2.50 per share, plus warrants to purchase approximately 532,000 shares of our common stock at an exercise price of $2.50 per share, valued at approximately $192,000. Warrants for 160,000 shares are exercisable at any time through September 29, 2008, and the remaining warrants for 372,000 shares become exercisable equally over five years and expire ten years from date of grant.

In addition to the purchase price for the above intellectual property, we agreed to pay a royalty fee to Tavad equal to three percent (3%) (six percent (6%) in Europe) of gross revenues from the PROMETA protocolsTreatment Programs using the acquired intellectual property for so long as we (or any licensee) use the acquired intellectual property. For purposes of the royalty calculations, gross revenue is defined as all payments made by patients for the treatment, including payments made to our licensees. Royalty fees, which totaled $192,000, $71,000 and $18,000 for the years ended December 31, 2007, 2006, 2005 and 2004,2005, respectively, are reflected in cost of services expense in the consolidated statements of operations as revenues are recognized.

In October 2004, the Technology Agreement was amended (Amendment) to expand the definition of “Processes,” limited to alcohol and cocaine in the original agreement dated March 2003, to also include crack cocaine and methamphetamine treatment processes, and the term “Intellectual Property” was expanded to include all improvements through September 14, 2004. As consideration for the Amendment, we paid $75,000 and issued 83,221 shares of our common stock, valued at $354,000.

Under the Technology Agreement, we are obligated to allocate each year a minimum of 50% of the funds we expend on sales, marketing, research and development to such activities relating to the use of the intellectual property acquired. If we do not expend at least the requisite percentage on such activities, the Tavad has the right to have the intellectual property revert to Tavad. We may terminate Tavad’s reversion rights by making an additional

F-16


payment of an amount which, taken together with previously paid royalties and additional payments, would aggregate $1.0 million. In  2004, 2005, 2006 and 20062007 we met our obligations with respect to this requirement.

The total cost of the assets acquired, plus additional costs incurred by us related to filing patent applications on such assets have been reflected in long-term assets as intellectual property. Amortization is being recorded on a straight-line basis over the remaining 16.5 year life of the pending patents, commencing July 1, 2003.

In May 2006, we issued 105,000 shares of our common stock valued at $738,000 to Tavad as initial consideration for a further amendment to the Technology Agreement.  The amendment expands the definition of “Processes” to include additional indications for the use of the PROMETA protocol.Treatment Program. The amendment


requires us to issue 35,000 shares for each indication for which we file a patent application claim, plus an additional 50,000 shares for each indication forfrom which we derive revenues in the future.

Patent for Opiate Addiction Treatment

In August 2003, we acquired a patent for a treatment method for opiate addiction at a foreclosure sale held by Reserva Capital, LLC, a company owned and controlled by our chief executive officer and substantialmajor shareholder, through a foreclosure sale in satisfaction of debt owed to Reserva by a XINO, medical technology development company. We paid approximately $314,000 in cash and agreed to issue 360,000 shares of our common stock to the technology development companyXINO at a future date conditional upon the occurrence of certain events, including a full release of claims by all of the technology development company’s creditors. As of December 31, 2006, such contingencies had not been satisfied, and we have not recorded any value for the shares that may be issued as additional consideration.

In December 2005, we evaluated our potential use of this patent and determined that it would not likely be utilized in our current business plan. Accordingly, we recorded an impairment charge of $272,000 in 2005 to write off the remaining capitalized costs of intellectual property relating to this patent. If and when it becomes probable that

On August 8, 2007, we willreached an agreement with XINO to release all or a portion310,000 of the 360,000 contingent shares which are currently subjectof our common stock previously issued to XINO. In consideration for a full release from the stock pledge agreement, XINO relinquished 50,000 of the previously issued shares and has agreed not to sell or transfer any of its 310,000 shares for a period of time following the settlement agreement, which expired in January 2008. We recorded the fair market value of the 310,000 shares released will be recordedissued as an additional non-cash impairment charge. Basedloss amounting to $2.4 million, based on ourthe closing stock price of $9.24$7.70 per share on December 31, 2006, the fair market value of the 360,000 contingent shares was approximately $3.3 million.August 8, 2007.

Treatment for Nicotine Dependence

In June 2005, we and a wholly-owned foreign subsidiary entered into an asset purchase agreement with Dr. Jacob Hiller to obtain the worldwide rights to his trade secret protocols for the treatment of nicotine and other dependencies, in exchange for a percentage of future net profits from exploitation of the protocols.  We have engaged Dr. Hiller as a consultant to explore opportunities in Europe to open treatment clinics for the treatment of dependencies using these protocols.
Amortization
Other Intangible Assets

In accordance with SFAS 141, “Business Combinations”, the purchase price for the CompCare acquisition was allocated to the fair values of the assets acquired, including identifiable intangible assets, in accordance with our proportionate share of ownership interest. These identified intangible assets include the value of managed care contracts and marketing-related assets associated with its managed care business, including the value of the healthcare provider network and the professional designation from the NCQA. Such assets will be amortized on a straight-line basis over their estimated remaining lives, which approximate the rate at which we believe the economic benefits of these assets will be realized.

Amortization

In accordance with SFAS 144, “Accounting for the Impairment or Disposal of Long-Lived Assets”,, we performed an impairment test and re-evaluated the useful lives and amortization methods on intellectual property and other intangible assets as of December 31, 2007. We determined that the estimated useful lives of intellectual property and other intangible assets properly reflected the current remaining economic useful lives of these assets.



Amortization expense for intellectual property wasall intangible assets amounted to $1.0 million, $217,000 $214,000 and $171,000$214,000 for the years ended December 31, 2007, 2006 and 2005, and 2004, respectively and is estimated to be $223,000respectively. Estimated amortization expense for each ofintangible assets for the next five years.years ending December 31, is as follows:
2008 $974,000
2009 $854,000
2010 $263,000
2011 $244,000
2012 $244,000
Note 7.  Debt Outstanding

On January 17, 2007, in connection with the Woodcliff acquisition, we entered into a securities purchase agreement pursuant to which we agreed to issue and sell to Highbridge International LLC (Highbridge) a $10 million senior secured note and a warrant to purchase up to approximately 250,000 shares of our common stock (together, the Financing). The accumulated amortizationnote bears interest at a rate of prime plus 2.5%, interest payable quarterly commencing on April 15, 2007 and matures on January 15, 2010. The current interest rate in effect at December 31, 2007 was 9.75%. The note is redeemable at our option anytime prior to maturity at a redemption price ranging from 103% to 110% of the principal amount during the first 18 months and is redeemable at the option of Highbridge beginning on July 17, 2008.

The Highbridge note restricts debt offerings so that we are only able to issue unsecured, subordinated debt so long as the principal payments are beyond the maturity of the Highbridge debt (January 15, 2010), and the interest rate is not greater than the Highbridge rate (Prime+2.5%).  The debt cannot have call rights during the Highbridge term and Highbridge must consent to the issuance of new debt.

The warrant has a term of five years, and was initially exercisable at $12.01 per share, or 120% of the $10.01 closing price of our common stock on January 16, 2007. Pursuant to an anti-dilution adjustment clause in the note, the exercise price of the warrant has been adjusted to $10.52 per share and the number of shares have been adjusted to 285,000, and is subject to further adjustments if we sell or are deemed to have sold shares at a price below the adjusted exercise price per share, and will be proportionately adjusted for stock splits or dividends. Similarly, if we were to issue convertible debt, the anti-dilution adjustment would also be triggered should the conversion price be less than $10.52 per share.

In connection with the financing, we entered into a security agreement granting Highbridge a first-priority perfected security interest in all of our assets now owned or thereafter acquired. We also entered into a pledge agreement with Highbridge, as collateral agent, pursuant to which we will deliver equity interests evidencing 65% of our ownership of our foreign subsidiaries. In the event of a default, the collateral agent is given broad powers to sell or otherwise deal with the pledged collateral. There are no material financial covenant provisions associated with this debt.

Total funds received of $10,000,000 were allocated to the warrant and the senior secured note in the amounts of $1,380,000 and $8,620,000, respectively, in accordance with their relative fair values as determined at the date of issuance. The value allocated to the warrant is being treated as a discount to the note and is being amortized to interest expense over the 18 month period between the date of issuance and the date that Highbridge has the right to redeem the note, using the effective interest method.  As of December 31, 2007, the unamortized discount on the senior secured notes is approximately $258,000. In addition, we paid a $150,000 origination fee and incurred approximately $150,000 in other costs associated with the financing, which have been allocated to the warrant and senior secured note in accordance with the relative fair values assigned to these instruments, and are being deferred and amortized over the 18 month period between the date of issuance and the date that Highbridge has the right to redeem the note.

As discussed more fully in Note 10 – Equity Financings, we entered into a redemption agreement with Highbridge to redeem $5 million in principal related to the senior secured notes as part of our securities offering completed on November 7, 2007. Included in the gross proceeds received on that date was $5.35 million for the conversion of $5 million of the senior note, which also included payment of $350,000 for an early redemption


penalty, based on a redemption price of 107% of the principal amount being redeemed pursuant to the redemption agreement. The $350,000 is included as part of the reacquisition cost of the notes and the difference between the reacquisition price and the net carrying amount of the principal amount being redeemed was recognized as a loss of $741,000 on extinguishment of debt in our statement of operations during the fourth quarter of 2007.
Debt outstanding also includes 7.5% convertible subordinated debentures of CompCare with a remaining principal balance of $2,244,000. As part of the purchase price allocation, an adjustment of $266,000 was made at the date of acquisition to reduce the carrying value of this debt to its estimated fair value. This adjustment is being treated as a discount and is being amortized over the remaining contractual maturity term of the note using the effective interest method.

The following table shows the total principal amount, related interest rates and maturities of debt outstanding, as of December 31, 2006 and 2005 was $591,000 and $374,000, respectively.
Note 6. Income Taxes2007:
 As of
Short-term Debt   
Senior secured note due January, 2010, interest payable quarterly at prime plus 2.5%, net of $258,000 unamortized discount
 $4,742,000 
     
Long-term Debt    
7.5% Convertible subordinated debentures due April, 2010, interest payable semi-annually, net of $187,000 unamortized discount (1)
 $2,057,000 

(1)  At December 31, 2006, we had net federal operating loss carry-forwards and state operating loss carry forwards2007, the debentures are convertible into 15,051 shares of approximately $63.7 and $61.6 million, respectively. The net federal operating loss carry forwards expire between 2023 and 2026, and net state operating loss carry forwards expire between 2013 and 2016. Foreign net operating loss carry-forwards were approximately $3.3 million,CompCare common stock at a conversion price of which $2.4 million will expire in seven years, $11,000 will expire in ten years, and $898,000 will carry forward indefinitely.

F-17


     The primary components of temporary differences which give rise to our net deferred tax are as follows:$149.09 per share.
         
  2006  2005 
Deferred tax assets:
        
Federal, state & foreign net operating losses $25,454,000  $13,281,000 
Stock-based compensation  2,810,000   1,283,000 
Accrued liabilities  481,000   425,000 
Other temporary differences  1,212,000   248,000 
Valuation allowance  (29,957,000)  (15,237,000)
       
  $  $ 
       

     We have provided a valuation allowance to fully offset our net deferred tax assets, in accordance with SFAS 109, because of our continued net losses, and management assessment of the realizability of our net deferred tax assets as being less than the more-likely-than-not criteria set forth in SFAS 109. Furthermore, certain portions of our net operating loss carry-forwards were acquired, and therefore subject to further limitation set forth under the Federal tax code which could further limit our ability to realize our deferred tax assets and provides that if there is a change in control for tax purposes the use of the net operating loss carry-forwards is limited per year.
     A reconciliation between the statutory federal income tax rate and the effective income tax rate is as follows for the years ended December 31:
             
  2006 2005 2004
Federal statutory rate  -34.0%  -34.0%  -34.0%
State taxes  -4.9%  -5.3%  -6.0%
Other  0.5%  -1.5%  0.0%
Change in valuation allowance  38.4%  40.8%  40.0%
             
   0.0%  0.0%  0.0%
             
Note 7.8.  Capital Lease Obligations

We lease certain furniture and computer equipment under agreements entered into during the fourth quarter of 2006 and 2007 that are classified as capital leases. The cost of furniture and computer equipment under capital leases is included in the Consolidated Balance Sheetsconsolidated balance sheets in property and equipment and was $236,000$741,000 at December 31, 2006.2007. Accumulated amortization of the leased equipment at December 31, 20062007 was approximately $10,000.$236,000. Amortization of assets under capital leases is included in depreciation expense.

The future minimum lease payments required under the capital leases and the present valuevalues of the net minimum lease payments, as of December 31, 2006,2007, are as follows (in thousands):
     
  Amount 
Year Ending December 31,
    
2007 $67 
2008  68 
2009  65 
2010  50 
2011  42 
    
Total minimum lease payments $292 
Less: Amount representing interest  (65)
    
Total capital lease obligations  227 
Less: Current maturities of capital lease obligations  (44)
    
Long-term capital lease obligations $183 
    

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Year Ending December 31,Amount 
2008 $233 
2009  187 
2010  111 
2011  76 
2012  - 
Total minimum lease payments$607 
 Less: Amount representing interest (93)
Total capital lease obligations 514 
 Less: Current maturities of capital lease obligations (183)
Long-term capital lease obligations$331 

Note 9.  Income Taxes

As of December 31, 2007, we had net federal operating loss carry-forwards and state operating loss carry forwards of approximately $100.0 million and $94.5 million, respectively. The net federal operating loss carry forwards expire between 2024 and 2027, and net state operating loss carry forwards expire between 2014 and 2017.  Foreign net operating loss carry-forwards were approximately $5.0 million, of which $4.6 million will expire in seven years, $19,000 will expire in ten years, and $400,000 will carry forward indefinitely.


The primary components of temporary differences which give rise to our net deferred tax are as follows:

  2007  2006 
Deferred tax assets:      
Federal, state & foreign net operating losses $39,542,000  $25,454,000 
Stock-based compensation  3,259,000   2,810,000 
Accrued liabilities  746,000   481,000 
Other temporary differences  (666,000 )  1,212,000 
Valuation allowance  (42,881,000)  (29,957,000)
  $-  $- 

    We have provided a valuation allowance to fully offset our net deferred tax assets, in accordance with SFAS 109, because of our continued net losses, and management assessment of the realizability of our net deferred tax assets as being less than the more-likely-than-not criteria set forth in SFAS 109. Section 382 of the Internal Revenue Code limits the use of net operating loss and tax credit carryforwards in certain situations where changes occur in the stock ownership of a company.  In the event we have a change in ownership, utilization of the carryforward could be restricted. We have not provided deferred taxes on CompCare, a less than 80% owned subsidiary, or our consolidated managed treatment centers accounted for under FIN 46R as these entities have accumulated book losses and we do not believe these losses can be realized for tax purposes in the foreseeable future.

A reconciliation between the statutory federal income tax rate and the effective income tax rate for the years ended December 31 follows:
 2007 2006
Federal statutory rate-34.0% -34.0%
State taxes-4.4% -4.9%
Other1.6% 0.5%
Change in valuation allowance36.8% 38.4%
 0.0% 0.0%

In June 2006, the FASB issued FIN 48 which clarifies the accounting for uncertainty in income taxes. FIN 48 requires that companies recognize in the consolidated financial statements the impact of a tax position, if that position is more likely than not of being sustained on audit, based on the technical merits of the position. FIN 48 also provides guidance on de-recognition, classification, interest and penalties, accounting in interim periods and disclosure. The provisions of FIN 48 are effective for years beginning after December 15, 2006. We adopted FIN 48 on January 1, 2007 with no impact to our consolidated financial statements. The Company and its subsidiaries file income tax returns in the U.S. federal jurisdiction and various state and foreign jurisdictions. Tax years that remain subject to examinations by tax authorities are 2003 through 2006.  The federal and material foreign jurisdictions statutes of limitations begin to expire in 2008.  There are no current income tax audits in any jurisdictions for open tax years and, as of December 31, 2007, there has been no material change to our FIN 48 position.

Note 8.10.  Equity Financings
     In December 2004, we issued 5,017,331 shares of common stock at a price of $4.50 per share in a private placement offering for a total of $22.6 million in proceeds from private investors, including two members of our board of directors who invested a total of $1.2 million. We paid $1.2 million in fees to placement agents in connection with the transaction.
In November 2005, we completed an underwritten public equity offering of 9,200,000 shares at a price of $4.75 per share for a total of $43.7 million in proceeds.  We paid $3.1 million in fees to the underwriters in connection with the transaction.

In December 2006, we issued 3,573,258 shares of common stock at a price of $7.30 per share in a private placement offering for a total of $26.1 million in proceeds. At December 31, 2006,We paid approximately $1.8 million in fees to placement agents and other transaction costs were owed in connection with the transaction.

In November 2007, we entered into securities purchase agreements with select institutional investors in a registered direct placement, in which we issued an aggregate of 9,635,000 shares of common stock at a price of $4.79 per share, for gross proceeds of approximately $46.2 million. We also issued 5-year warrants to purchase an aggregate of approximately 2.4 million additional shares of our common stock at an exercise price of $5.75 per share. The fair value of the warrants at the date of issuance was estimated at $6.3 million and was accounted for as a


liability pursuant to EITF 00-19. We incurred $3.7 million in fees to placement agents and other offering expenses in connection with the transaction. Included in the gross proceeds was $5.35 million from the conversion of $5 million of the senior secured notes issued to Highbridge, pursuant to a redemption agreement entered into with Highbridge on November 7, 2007 See Note 7 Debt Outstanding.

Note 9.11.  Share-based Compensation

The Hythiam, Inc. 2003 and 2007 Stock Incentive PlanPlans (the Plan), as amended, providesPlans) provide for the issuance of up to 79 million shares of our common stock. Incentive stock options and(ISOs) under Section 422A of the Internal Revenue Code, non-qualified options (NSOs), stock appreciation rights, limited stock appreciation rights, and restricted stock grants are authorized under the Plan.Plans. We grant all such share-based compensation awards at no less than the fair market value of our stock on the date of grant, and have granted stock and stock options to executive officers, employees, members of our board of directors, and certain outside consultants. The terms and conditions upon which options become exercisable vary among grants, however, option rights expire no later than ten years from the date of grant and employee and board of director awards generally vest on a straight-line basis over five and four years, respectively. At December 31, 2006,2007, we had 6,305,0006,257,000 vested and unvested stock options outstanding (vested and unvested) and 423,0001,904,000 shares reserved for future awards. Total share-based compensation expense on a consolidated basis amounted to $2.6 million, $3.7 million and $1.3 million for the years ended December 31, 2007, 2006 and 2005.

Stock Options Employees and Directors

During the2007, 2006 2005 and 2004,2005, we granted options to employees and directors for 732,000, 1,657,000 1,317,000 and 1,404,0001,317,000 shares, respectively, to employees and directors at the weighted average per share exercise prices of $7.08, $6.27 $6.49 and  $4.24,$6.49, respectively, the fair market value of our common stock on the dates of grants.  The estimated fair value of options granted to employees and directors during 2007, 2006 and 2005 and 2004 was $3.3 million, $6.6 million $5.4 million and $3.6$5.4 million, respectively, calculated using the Black-Scholes pricing model with the assumptions described in Note 1 “Share-based Compensation”.- Share-based Compensation.  Stock option activity under the Plan for the three years ended December 31, 20062007 was as follows:

F-19



         
      Weighted Avg. 
  Shares  Exercise Price 
Balance, December 31, 2003  3,195,000  $2.58 
         
2004
        
Granted  1,404,000   4.24 
Exercised      
Cancelled  (542,000)  3.69 
       
Balance, December 31, 2004  4,057,000  $3.01 
       
         
2005
        
Granted  1,317,000  $6.49 
Exercised  (54,000)  3.29 
Cancelled  (422,000)  4.88 
       
Balance, December 31, 2005  4,898,000  $3.78 
       
         
2006
        
Granted  1,657,000  $6.27 
Exercised  (80,000)  3.75 
Cancelled  (647,000)  5.34 
       
Balance, December 31, 2006  5,828,000  $4.32 
       
     Weighted Avg. 
  Shares  Exercise Price 
Balance, December 31, 2004  4,057,000  $3.01 
         
2005        
Granted  1,317,000   6.49 
Exercised  (54,000)  3.29 
Cancelled  (422,000)  4.88 
Balance, December 31, 2005  4,898,000  $3.78 
         
2006        
Granted  1,657,000  $6.27 
Exercised  (80,000)  3.75 
Cancelled  (647,000)  5.34 
Balance, December 31, 2006  5,828,000  $4.32 
         
2007        
Granted  732,000  $7.08 
Transfer *  (695,000)  5.10 
Exercised  (483,000)  3.14 
Cancelled  (230,000)  6.47 
Balance, December 31, 2007  5,152,000  $4.61 
         
* Option transfer due to status change from employee to non-employee. 



The weighted average remaining contractual life and weighted average exercise price of options outstanding as of December 31, 20062007 were as follows:
                     
  Options Outstanding Options Exercisable
      Weighted        
      Average Weighted     Weighted
      Remaining Average     Average
Range of Exercise Prices Shares Life (yrs) Price Shares Price
$2.50 to $3.50  3,098,000   6.8  $2.61   1,917,000  $2.61 
$3.51 to $4.50  144,000   7.8   4.25   70,000   4.25 
$4.51 to $5.50  571,000   9.6   4.77       
$5.51 to $6.50  1,017,000   7.9   5.90   187,000   5.72 
$6.51 to $7.50  540,000   7.9   7.32   129,000   7.39 
$7.51 to $8.50  434,000   9.9   7.89   116,000   7.89 
$8.51 to $9.50  24,000   9.3   8.56       
                     
   5,828,000           2,419,000     
                     

   Options Outstanding   Options Exercisable
Range of Exercise Prices Shares Weighted Average Remaining Life (yrs)
Weighted
Average Price
Shares Weighted Average Price
            
 $2.50 to $3.50 2,435,000 5.8  $      2.62 1,954,000  $        2.61
 $3.51 to $4.50 189,000 8.7 4.13 44,000 4.25
 $4.51 to $5.50 565,000 8.6 4.77 113,000            4.77
 $5.51 to $6.50 717,000 7.5 6.08 285,000 5.92
 $6.51 to $7.50 583,000 8.3 7.24 133,000 7.30
 $7.51 to $8.50 582,000 9.0 7.92 172,000 7.89
 $8.51 to $9.50 81,000 9.2 9.00               -                -
   5,152,000 7.1          4.61 2,701,000            3.64

At December 31, 20052007 and 2004,2006, the number of options exercisable werewas 2,419,000 and 1,430,000, and 729,000, respectively, at weighted-average exercise prices of $2.87$3.76 and $2.66,$2.87, respectively.

As a result of adopting SFAS 123R on January 1, 2006, share-based expense relating to stock options granted to employees and directors was $2.4 million and $2.3 million for the year.year ended December 31 2007 and 2006, respectively.

As of December 31, 2006,2007, there was $8.9$7.0 million of total unrecognized compensation costs related to non-vested share-based compensation arrangements granted under the Plan.Plans. That cost is expected to be recognized over a weighted-average period of 3.23.09 years.

F-20



Stock Options and Warrants Non-employees

In addition to stock options granted under the Plan,Plans, we have also granted options and warrants to purchase our common stock to certain non-employees that have been approved by our board of directors.  During 2007, 2006 2005 and 2004,2005, we granted options and warrants for 65,000, 368,000 110,000 and 370,000110,000 shares, respectively.



Stock option and warrant activity for non-employee grants for services is summarized as follows:
         
      Weighted Avg. 
  Shares  Exercise Price 
Balance, December 31, 2003  1,979,000  $2.52 
         
2004
        
Granted  370,000   5.05 
Exercised  (27,000)  2.50 
Cancelled      
       
Balance, December 31, 2004  2,322,000  $2.92 
       
         
2005
        
Granted  110,000  $5.32 
Exercised  (116,000)  2.50 
Cancelled  (314,000)  2.50 
       
Balance, December 31, 2005  2,002,000  $3.15 
       
         
2006
        
Granted  368,000  $4.96 
Exercised  (603,000)  2.53 
Cancelled  (372,000)  3.78 
       
Balance, December 31, 2006  1,395,000  $3.72 
       

     Weighted Avg. 
  Shares  Exercise Price 
Balance, December 31, 2004  2,322,000  $2.92 
         
2005        
Granted  110,000   5.32 
Exercised  (116,000)  2.50 
Cancelled  (314,000)  2.50 
Balance, December 31, 2005  2,002,000  $3.14 
         
2006        
Granted  368,000  $4.96 
Exercised  (603,000)  2.53 
Cancelled  (372,000)  3.78 
Balance, December 31, 2006  1,395,000  $3.72 
         
2007        
Granted  65,000  $7.47 
Transfer *  695,000   5.10 
Exercised  (104,000)  4.57 
Cancelled  (42,000)  6.24 
Balance, December 31, 2007  2,009,000  $4.22 
         
* Option transfer due to status change from employee to non-employee. 

Stock options and warrants granted to non-employees for services, debt agreement and offerings outstanding at December 31, 20062007 are summarized as follows:
             
      Weighted    
      Average  Weighted 
      Remaining  Average 
      Contractual  Exercise 
Description Shares  Life (yrs)  Price 
Warrants issued for intellectual property  532,000   5.2  $2.50 
Warrants issued in connection with equity offering  111,000   2.7   2.89 
Options and warrants issued to consultants  752,000   2.7   4.71 
          
   1,395,000   3.7  $3.72 
          

Description Shares  Weighted Average Remaining Contractual Life (yrs)  Weighted Average Exercise Price 
Warrants issued for intellectual property 532,000  4.2  $2.50 
Warrants issued in connection with equity offering 2,515,000  4.7   5.64 
Warrants issued in connection with debt agreement 285,000  4.1   10.52 
Options and warrants issued to consultants 1,362,000  4.5   5.02 
  4,694,000  4.5  $5.40 
           

Share-based expense relating to stock options and warrants granted to non-employees amounted to ($14,000), $1.2 million and $1.6 million for 2007, 2006 and $1.1 million for 2006, 2005, and 2004, respectively.  At December 31, 2006,2007, unvested options and warrants had an estimated value of approximately $1.3 million,$277,000, using the Black-Scholes pricing model.

Common Stock

During 2007, 2006 2005 and 2004,2005, we issued 30,000, 51,000 23,000 and 17,00023,000 shares of common stock, respectively, for consulting services, valued at $239,000, $326,000 $134,000 and $86,000,$134,000, respectively. These costs are amortized to share-based expense on a straight-line basis over the related service periods generally ranging from six months to one year. Share-based expense relating to all common stock issued for consulting services was $118,000, $229,000 and $134,000 for 2007, 2006 and $86,000 for 2006, 2005, and 2004, respectively.

F-21





Employee Stock Purchase Plan

In June 2006, we adopted a qualified employee stock purchase plan (Stock Purchase Plan)(ESPP), approved by our board of directors and shareholders, which provides that eligible employees (employed at least 90 days) have the option to purchase shares of our common stock at a price equal to 85% of the of the lesser of the fair market value as of the first day or the last day of each offering period. Purchase options are granted bi-annually and are limited to the number of whole shares that can be purchased by an amount equal to up to 10% of a participant’s annual base salary.  As of December 31, 2007, there were 27,000 shares of our common stock issued pursuant to the ESPP. Share-based expense relating to the ESPP was $15,000 for the year ended December 31, 2007. There was no expense in 2006 associated with the ESPP.

Stock Options – CompCare Employees, Directors and Consultants
CompCare’s 1995 and 2002 Incentive Plans (the CompCare Plans) provide for the issuance of up to 1 million shares of CompCare common stock for each plan. ISOs, NSOs, stock appreciation rights, limited stock appreciation rights, and restricted stock grants to eligible employees and consultants are authorized under the CompCare Plans. CompCare issues stock options to its employees and non-employee directors allowing them to purchase common stock pursuant to the CompCare Plans.  Options for ISOs may be granted for terms of up to ten years and are generally exercisable in cumulative increments of 50% each six months. The exercise price for ISOs must equal or exceed the fair market value of the shares on the date of grant.  The Plans also provide for the full vesting of all outstanding options under certain change of control events. As of December 31, 2007, under the 2002 Plan, there were 500,000 options available for grant and there were 460,000 options outstanding, of which 440,000 are exercisable.  Additionally, as of December 31, 2007, under the 1995 Plan, there were 485,000 options outstanding and exercisable. The 1995 Plan was terminated effective August 31, 2005 such that there are no further options available for grant under this plan.

CompCare also has a non-qualified stock option plan for its outside directors (the CompCare Directors’ Plan). Each non-qualified stock option is exercisable at a price equal to the average of the closing bid and asked prices of the common stock in the over-the-counter market for the last preceding day there was a sale of the stock prior to the grant date. Grants of options vest in accordance with vesting schedules established by CompCare’s Compensation and Stock Option Committee.  Upon joining the CompCare Board, directors receive an initial grant of 25,000 options.  Annually, directors are granted 15,000 options on the date of CompCare’s annual meeting. As of December 31, 2007, under the Directors’ Plan, there were 777,000 shares available for option grants and 125,000 options outstanding, of which none are exercisable.

CompCare stock option activity for the period January 13 through December 31, 2007 was as follows:
  Shares  Weighted Avg. Exercise Price 
Balance, January 13, 2007 1,166,000  $1.32 
Granted 145,000   1.05 
Exercised (37,000)  0.51 
Cancelled (204,000)  1.77 
        
Balance, December 31, 2007 1,070,000  $1.23 
Stock options totaling 145,000 were granted to board of director members and certain employees during the period January 13 through December 31, 2007 at a weighted average grant-date fair value of $1.05. A total of 37,000 options were exercised during the period January 13 through December 31, 2007, which had a total intrinsic value of $13,000. During the period January 13 through December 31, 2007, 123,000 stock options granted to directors and one officer expired unexercised. For the period January 13 through December 31, 2007, 81,000 stock options granted to certain CompCare board of director members and employees, respectively, were cancelled due to the recipients’ resignation from the CompCare board of directors or CompCare.



At December 31, 2007, there was approximately $59,000 of total unrecognized compensation cost related to unvested options, which is expected to be recognized over a weighted-average period of approximately 6 months. Total recognized compensation costs during the period January 13 through December 31, 2007 were $83,000. No compensation cost related to employees was recognized prior to June 1, 2006.

The following table summarizes information about options granted, exercised, and vested for the period January 13 through December 31, 2007 is as follows:

  
For the period
January 13
through 
December 31, 2007
Options granted  145,000
Weighted-average grant-date fair value $0.76
Options exercised  37,000
Total intrinsic value of exercised options $13,000
Fair value of vested options $11,000
A summary of options outstanding and exercisable as of December 31, 2007 is as follows:
   Options Outstanding   Options Exercisable
Range of Exercise Prices Shares Weighted Average Remaining Life (yrs)Weighted Average PriceShares Weighted Average Price
            
 $0.25 to $0.27 182,000 2.59  $      0.26 182,000  $        0.26
 $0.39 to $0.56 261,000 2.47 0.54 261,000            0.54
 $0.78 to $1.12 189,000 8.90 1.07 44,000 1.10
 $1.40 to $1.78 247,000 6.76 1.62 247,000 1.62
 $1.80 to $2.16 94,000 7.40 1.95 94,000 1.95
 $3.56 to $4.00 97,000 0.95 3.95       97,000            3.95
   1,070,000 4.91  $      1.27 925,000  $        1.30
Warrants

CompCare periodically issues warrants to purchase common stock as compensation for the services of consultants and marketing employees.  Of the 406,000 warrants outstanding at December 31, 2007, 306,000 were issued to two consultants and two employees as compensation for introducing strategic business partners to CompCare. Such partners were responsible for the infusion of approximately $776,000 in cash to CompCare in February and March 2005 in a private placement of CompCare’s common stock. All such warrants have five-year terms. Valuation using the Black-Scholes pricing model for the warrants issued in February and March of 2005 was based on the following information:

Number of warrants  306,000 
Exercise price $1.25 
Volatility factor of CompCare's common stock  95%
Expected life of the warrants 3 years 
Risk-free interest rate  3.9%
Dividend yield  0.0%
Warrant valuation (in thousands) $234 
No warrants were issued during the period January 13 through December 31, 2007.



Note 12. Segment Information

We manage and report our operations through two business segments: healthcare services and behavioral health managed care services.

Our healthcare services segment is focused on delivering solutions for those suffering from alcohol, cocaine, methamphetamine and other substance dependencies by researching, developing, licensing and commercializing innovative physiological, nutritional, and behavioral treatment programs. Treatment with our PROMETA Treatment Programs, which integrate behavioral, nutritional, and medical components, are available through physicians and other licensed treatment providers who have entered into licensing agreements with us for the use of our treatment programs. Also included in this segment are licensed and managed treatment centers, which offer a range of addiction treatment services, including the PROMETA Treatment Programs for dependencies on alcohol, cocaine and methamphetamines.

Our healthcare services segment also comprises international and government sector operations; however, these operating segments are not separately reported as they do not meet any of the quantitative thresholds under SFAS 131, “Disclosures about Segments of an Enterprise and Related Information.”

The behavioral health managed care services segment is focused on providing managed care services in the behavioral health and psychiatric fields, and principally includes the operations of our majority-owned, controlled subsidiary, CompCare, which was acquired on January 12, 2007. CompCare manages the delivery of a continuum of psychiatric and substance abuse services to commercial, Medicare and Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators, and commercial and other group purchasers of behavioral healthcare services.  The customer base for CompCare’s services includes both private and governmental entities. We also plan to offer disease management programs for substance dependence built around our proprietary PROMETA Treatment Program for alcoholism and dependence to stimulants as part of our behavioral health managed care services operations. 

We evaluate segment performance based on total assets, revenues and net income or loss before taxes. Our assets are included within each discrete reporting segment. In the event that any services are provided to one reporting segment by the other, the transaction is valued at the market price. No such services were provided during the year ended December 31, 2007.

Summary financial information for our two reportable segments is as follows:

   Year Ended December 31, 
  2007  2006  2005 
Behavioral health managed care services (1)         
Revenues $36,306,000  $-  $- 
Loss before provision for income taxes  (4,105,000)  -   - 
Assets *  8,896,000   -   - 
             
Healthcare services            
Revenues $7,695,000  $3,906,000  $1,164,000 
Loss before provision for income taxes  (41,270,000)  (38,296,000)  (24,038,000)
Assets *  61,750,000   52,205,000   54,462,000 
             
Consolidated operations            
Revenues $44,001,000  $3,906,000  $1,164,000 
Loss before provision for income taxes  (45,375,000)  (38,296,000)  (24,038,000)
Total Assets *  70,646,000   52,205,000   54,462,000 
             
* Assets are reported as of December 31.            
(1) Results for the year in this segment represent the period January 13 through December 31, 2007. 



Note 13. Major Customers/Contracts

For the period January 13 through December 31, 2007, 87% of revenue in our behavioral health managed care services segment (72% of consolidated revenues for the year ended December 31, 2007) was concentrated in CompCare’s contracts with six health plans to provide behavioral healthcare services under commercial, Medicare, Medicaid, and children’s health insurance plans (CHIP). This includes the contracts discussed below.

In January 2008, an existing Medicare Advantage HMO client issued a request for proposal (RFP) for renewal of a contract for management of behavioral healthcare services for its Pennsylvania, Maryland, and Texas regions. Revenues under the contracts accounted for $5.4 million, or 15% of our behavioral heath managed care services revenues for the period January 13 through December 31, 2007 (12% of consolidated revenues for the year ended December 31, 2007). CompCare ceased providing services to the client’s Texas membership as of December 31, 2006. CompCare  submitted a bid to retain its current business with this client as well as attempt to regain the Texas membership. This client intends to select a finalist in March 2008 with an effective date of July 1, 2008 for a new agreement to serve members in these states. CompCare does not expect to be selected as a finalist and accordingly the majority of the revenues under this contract are expected to end during the third quarter of 2008.
    In January 2007, CompCare began providing behavioral health services to approximately 250,000 Indiana Medicaid recipients pursuant to a contract with an Indiana HMO. The contract accounted for approximately $14.6 million or 40% of our behavioral health managed care services revenues for the period January 13 through December 31, 2007 (or 33% of consolidated revenues for the year ended December 31, 2007), and is for an initial term of two years with subsequent extensions by mutual written agreement. To offset high utilization costs during 2007, CompCare is negotiating and believes it will receive a rate increase effective January 1, 2008, provided it complies with monthly performance measures it believes it will meet. The rate increase would amount to approximately $2.0 million per annum.

CompCare currently furnishes behavioral healthcare services to approximately 244,000 members of a health plan providing Medicaid, Medicare, and CHIP benefits in Michigan, Texas and California.  Services are provided on a fee-for-service and Administrative Services Organization (ASO) basis.  The contracts accounted for $4.2 million, or 12% of behavioral health managed care service revenues for the period January 13 through December 31, 2007 (10% of consolidated revenues for the year ended December 31, 2007).  The initial offeringcontract, which commenced in June of 2002, was for a one-year period for the Stock Purchase Plan commencedand has been automatically renewed on September 1, 2006, and ended on January 1, 2007. Payroll deductions relatedan annual basis.  Termination by either party may occur with 90 days written notice to the stock purchase plan were not material in 2006.other party.

In general, CompCare’s contracts with its customers are typically for initial one-year terms, with automatic annual extensions.  Such contracts generally provide for cancellation by either party with 60 to 90 days written notice.

Note 10.14.  Commitments and Contingencies

Operating Lease Commitments

We incurred rent expense of approximately $1.4 million, $911,000 $646,000 and $378,000,$646,000 for the years ended December 31, 2007, 2006 2005 and 2004,2005, respectively. In September 2003, we signed a lease agreement for our corporate offices at an initial lease cost of approximately $33,000 per month, with increases scheduled annually over the lease term. The term of the lease is seven years beginning on the lease commencement date, December 15, 2003, and includes a right to extend the lease for an additional five years. In April, 2005 we amended the lease to expand our corporate office facilities at an additional base rent of approximately $11,000 per month, subject to annual adjustment over the remaining initial six-year term.  As a condition to signing the original lease agreement, we secured a $350,000 letter of credit at the current amount of $262,500 for the landlord as a form of security deposit. The letter of credit is collateralized by a certificate of deposit in the amount of $350,000,$262,500, which is included in deposits and other assets in the consolidated balance sheets as of December 31, 2006.2007.

In April 2005 we entered into a five year lease for approximately 5,400 square feet of medical office space at an initial base rent of approximately $19,000 per month commencing in August 2005.  The space is occupied by The PROMETA Center, a managed medical practice, under a full business service management agreement.  As a condition to signing the lease, we secured a $90,000 letter of credit for the landlord as a form of security deposit.


The letter of credit is collateralized by a certificate of deposit in the amount of $90,000, which is included in deposits and other assets in the consolidated balance sheet as of December 31, 2006.2007.

In August 2006, we entered into a 62 month lease for approximately 4,000 square feet of medical office space, located in San Francisco, California, at an initial base rent of approximately $11,000 per month, commencing in January 2007.  The space iswas occupied by the PROMETA Center through January 31, 2008 under an amendment to our management service agreement. We are currently seeking to sublease the vacant space.

In connection with a management services agreement that we executed with a medical professional corporation in Dallas, Texas, we assumed the obligation for two lease agreements at a current combined amount of approximately $9,000 per month, which expire in May 2011.

In November 2006, we entered into a 5 year lease for office space in Switzerland at an initial base rent of 4,052 Swiss Francs per month (US$3,325 using the December 31, 2006 conversion rate).

CompCare leases certain office space and equipment.  The Texas office lease contains escalation clauses based on the Consumer Price Index and provisions for payment of real estate taxes, insurance, and maintenance and repair expenses.  Total rental expense for all CompCare operating leases was $259,000 for the period January 13 through December 31, 2007. This expense does not include rent payments related to the Company’s use of space within the offices of its major Indiana client, which is not subject to a written lease agreement.

Rent expense is calculated using the straight-line method based on the total minimum lease payments over the initial term of the lease. Unamortized landlord tenant improvement allowances and rent expense exceeding actual rent payments are accounted for as deferred rent liability in the balance sheet.

Future minimum payments, by year and in the aggregate, under non-cancelable operating leases with initial or remaining terms of one year or more, consist of the following at December 31, 2007:
  Operating 
  Leases 
Year Ending December 31, (000's) 
2008 $1,624 
2009  1,364 
2010  1,246 
2011  250 
2012  158 
Total minimum lease payments $4,642 

Clinical Research Commitments

In 20052006 and 2006,2007, we committed to a number of unrestricted grants for clinical research studies by preeminent researchers in the field of substance dependence and leading research institutions to evaluate the efficacy of our PROMETA protocolsTreatment Programs in treating alcohol and stimulant dependence. As of December 31, 2006,2007, we have approximately $5.9$4.1 million committed to such clinical research studies, with approximately $5.2 million to be paid in 2007 and the remaining balanceall of $700,000which is expected to be paid in 2008.

F-22



Other Commitments and Contingencies

CompCare provided behavioral healthcare services to the members of a Connecticut HMO from 2001 to 2005 under a contract that provided that CompCare would also receive funds directly from a state reinsurance program for the purpose of paying providers.  At December 31, 2007, $2.5 million of reinsurance claims payable remains and is attributable to providers having submitted claims for authorized services having incorrect service codes or otherwise incorrect information that has caused payment to be denied by us.  In such cases, there are


statutory provisions that allow the provider to appeal a denied claim.  If no appeal is received by the Company within the prescribed amount of time, it is probable that CompCare will be required to remit the reinsurance funds back to the appropriate party.

In connection with CompCare’s Indiana contract that started January 1, 2007, CompCare is required to maintain a performance bond in the amount of $1,000,000. In addition, a $25,000 performance bond is maintained in relation to a Third Party Administrator license in Maryland.  Relating to this contract, CompCare has become aware that the state of Indiana is considering requiring payment of a claims billing code that CompCare had previously been instructed to deny. If the state of Indiana implements the payment requirement, the claims represented by these billing codes would be paid retroactively to January 1, 2007.  Although CompCare does not believe they have a contractual obligation to pay for this code, it is possible that CompCare might be responsible for these payments, which in CompCare’s estimation could approximate $350,000. CompCare believes that the state of Indiana will make a final determination by mid-April 2008.

Related to CompCare’s discontinued hospital operations, Medicare guidelines allow the Medicare fiscal intermediary to re-open previously filed cost reports. CompCare’s fiscal 1999 cost report, the final year CompCare was required to file a cost report, is being reviewed, in which case the intermediary may determine that additional amounts are due to or from Medicare. CompCare management believes cost reports for fiscal years prior to fiscal 1999 are closed and considered final.

Legal Proceedings

From time to time, we may be involved in litigation relating to claims arising out of our operations in the normal course of business. As of the December 31, 2006,2007, we were not involved in any legal proceeding that we believe would have a material adverse effect on our business, financial condition or operating results.

 CompCare may incur further legal defense fees and may be subject to awards of plaintiff’s attorney fees or other fees, the amounts of which are not reasonably estimable.  See Part I, Item 3, “Legal Proceedings” for a description of these matters.

Note 11.15.  Related Party Transactions

Andrea Grubb Barthwell, M.D., a member of our Board of Directors, is the founder and chief executive officer of a healthcare and policy consulting firm providing consulting services to us.  In 20062007 and 2005,2006, we paid or accrued approximately $189,000$156,000 and $83,000,$189,000, respectively, in fees to the consulting firm.

There were no other material related party transactions in 2007, 2006 2005 or 2004.2005.

Note 12.16.  Subsequent Events (Unaudited)
Acquisition of Woodcliff
In January 2008 we streamlined our operations to increase our focus on disease management and Controlling Interest in CompCare
     On January 11, 2007, we entered into a letter of intent with Woodcliff Healthcare Investment Partners, LLC (Woodcliff) and its membersmanaged care opportunities, which is expected to acquire all of its outstanding membership interests in exchange for $9 million in cash and 215,053 shares of our common stock to be registered for resale. On January 12, 2007, we then entered into a Limited Liability Company Membership Interest Purchase Agreement containing customary terms and conditions, including representations, warranties and indemnities, and closed the acquisition.
     Woodcliff owns 1,739,130 shares of common stock and 14,400 shares of Series A Convertible Preferred Stock of Comprehensive Care Corporation, a Delaware corporation (CompCare), the conversion of which would result in Woodcliff owning over 50%an overall reduction of 25% to 30% of cash operating expenses for the outstanding shares of common stock of CompCare.fiscal year ending December 31, 2008. The preferred stock has voting rightsactions we took included eliminating field and combinedregional sales personnel and related corporate support personnel, closing the PROMETA Center in San Francisco, a reduction in outside consultants and overall reductions in overhead costs.  Estimated one-time costs associated with the common shares held by Woodcliff, gives us voting control over CompCare. The purchase price was equal to $667.27 per share of preferred stock and $0.80 per share of common stock of CompCare owned by Woodcliff.
     On January 18, 2007, we entered into an Agreement and Plan of Merger, and on January 26, 2007 we entered into an amended and restated Agreement and Plan of Merger, with CompCare, pursuant to which we would acquire the remaining outstanding shares of CompCare. The merger agreement provides that the parties may terminate the agreement by mutual written consent at any time prior to consummation of the merger, whether before or after stockholder approval. Litigation to enjoin the merger is currently pending, and it is unclear at this time whether the merger will proceed or if the merger agreement will be terminated by the parties.
     CompCare, primarily through its wholly-owned subsidiary, Comprehensive Behavioral Care, Inc., provides managed care services in the behavioral health and psychiatric fields. CompCare manages the delivery of a continuum of psychiatric and substance abuse services to commercial, Medicare and Medicaid members on behalf of employers, health plans, government organizations, third-party claims administrators, and commercial and other group purchasers of behavioral healthcare services. The customer base for CompCare’s services includes both private and governmental entities. CompCare’s services are provided primarily by unrelated vendors on a subcontract basis. CompCare is currently a licensee of our PROMETA protocols to treat patients managed by CompCare.
     The Woodcliff acquisition will be accounted for as a purchase. As a result of our acquisition of Woodcliff, we control CompCare and will consolidate its results of operations starting on January 12, 2007.
Acquisition Financing
     On January 17, 2007, in connection with the acquisition, we entered into a Securities Purchase Agreement pursuant to which we agreed to issue and sell to Highbridge International LLC (a) $10these actions were approximately $1.0 million original principal amount of senior secured notes and (b) warrants to purchase up to 249,750 shares of our common stock. The note bears interest at a rate of prime plus 2.5%, interest payable quarterly commencing on April 15, 2007, and matures on

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January 15, 2010. The warrants have a term of five years, and are exercisable at $12.01 per share, or 120% of the $10.01 closing price on January 16, 2007. The exercise price of the warrant will be reduced if we sell or are deemed to have sold shares at a lower price, and will be proportionately adjustedrecognized as a charge to operating expenses in the statement of operations for stock splits or dividends.the quarter ended March 31, 2008. Such costs primarily represent severance and related benefits and costs incurred to close the San Francisco PROMETA Center. We do not expect to incur any material additional costs associated with this initiative.  
     In connection with the financing, we entered into a Security Agreement granting Highbridge a first-priority perfected security interest in all


Note 13.17.  Interim Financial Information (Unaudited)

Summarized quarterly supplemental financial information is as follows:
                     
  Quarter Ended Total
  March June September December Year
  (In thousands, except per share amounts)
Year Ended December, 31, 2006
                    
Revenues $653  $1,172  $1,071  $1,010  $3,906 
Loss from operations  (9,204)  (9,394)  (10,212)  (11,116)  (39,926)
Net loss  (8,728)  (8,962)  (9,829)  (10,779)  (38,298)
Basic and diluted loss per share  (0.22)  (0.23)  (0.25)  (0.27)  (0.96)
                     
Year Ended December, 31, 2005
                    
Revenues $203  $230  $361  $370  $1,164 
Loss from operations  (4,480)  (4,866)  (6,756)  (8,770)  (24,872)
Net loss  (4,319)  (4,692)  (6,604)  (8,423)  (24,038)
Basic and diluted loss per share  (0.15)  (0.16)  (0.22)  (0.24)  (0.77)

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  Quarter Ended    Total 
  March  June  September   December     Year 
  (In thousands, except per share amounts)      
Year Ended December, 31, 2007                  
Revenues $8,857  $11,340  $12,020   $11,784    $44,001 
Loss from operations  (10,772)  (12,020)  (13,473)(a)  (11,266)    (47,531)
Net loss  (10,743)  (12,252)  (13,843)(a)  (8,624)(b)(c)  (45,462)
Basic and diluted loss per share  (0.25)  (0.28)  (0.31)(a)  (0.17)(b)(c)  (0.99)
                        
Year Ended December, 31, 2006                       
Revenues $653  $1,172  $1,071   $1,010    $3,906 
Loss from operations  (9,204)  (9,394)  (10,212)   (10,486)    (39,296)
Net loss  (8,728)  (8,962)  (9,829)   (10,779)    (38,298)
Basic and diluted loss per share  (0.22)  (0.23)  (0.25)   (0.27)    (0.96)
(a)  Includes a $2.4 million impairment loss related to the non-cash stock settlement reached with XINO Corporation in August 2007.  See further discussion in Note 6 – Intangible Assets.

(b)  The fair value of warrants issued in conjunction with the registered direct placement in November 2007 was accounted for as a liability and was revalued at $2.8 million at December 31, 2007, resulting in $3.5 million non-operating gain.

(c)  Includes a loss of $741,000 on extinguishment of debt resulting from the redemption of $5 million in Highbridge senior secured notes in November 2007.  See further discussion in Note 7 – Debt Outstanding.

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