UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM. 10-QSB [ X ] QUARTERLY REPORTS UNDER SECTION 13 OR 15(D) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE QUARTERLY PERIOD ENDED December 31, 2001. OR [ ] QUARTERLY REPORTS UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE TRANSITION PERIOD FROM ____________ TO ______________.
PARACELSIAN, INC. |
Delaware | 16-1399565 | |
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(State or other jurisdiction of incorporation or organization) | (I.R.S. Employer Identification No.) | |
222 Langmuir Laboratories, | 14850 | |
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(Address of principal executive offices) | Zip Code | |
Issuer's telephone number: (607) 257-4224 -------------------------------------------------------------------- | ||
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Check whether the issuer (1) filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act during the past 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. Yes [ ] No [ X ] There were 23,929,388 shares of Common Stock outstanding at February 1, 2002
(PAGE 1) Paracelsian, Inc. and Subsidiary Index | |
Page | |
PART I. - FINANCIAL INFORMATION Item 1. Financial Statements | |
Consolidated Balance Sheet as of December 31, 2001 (Unaudited) | 3 |
Consolidated Statements of Operations for the three months ended December 31, 2001 | 4 |
Consolidated Statements of Cash Flows for the three months ended December 31, 2001 and 2000 and the cumulative period from inception to December 31, 2001 (Unaudited) | 5 |
Notes to Consolidated Financial Statements (Unaudited) | 6 |
Item. 2 — Management’s Discussion and Analysis of Financial Condition and Results of Operations | 9 |
PART II — OTHER INFORMATION | |
Item 1 — Legal Proceedings | 10 |
Item 6 — Exhibits and Reports of Form 8-K | 11 |
Signatures | 11 |
Paracelsian, Inc. and Subsidiary |
December 31, 2001 | ||||
Assets | ||||
Current Assets: | ||||
Cash and cash equivalents | $ | 17,338 | ||
Prepaid expenses | 38,350 | |||
Other current assets | 41,769 | |||
| Total current assets | 97,457 | ||
Equipment, net | 49,616 | |||
Interest Receivable, net of reserve of $62,465 | - | |||
Note Receivable, net of reserve of $148,750 | - | |||
Other Assets: | ||||
Patents and trademarks, net | 74,611 | |||
124,227 | ||||
$ | 221,684 | |||
Liabilities and Stockholders' Deficit | ||||
Current Liabilities: | ||||
Accounts payable | $ | 335,395 | ||
Accrued expenses | 637,639 | |||
Current portion of capital lease obligation | 1,074 | |||
Current portion of notes payable | 137,068 | |||
Current portion of deferred revenue | 29,976 | |||
Advances from related party | 310,677 | |||
Total current liabilities | 1,451,829 | |||
Long-term portion of capital lease obligation | 346 | |||
Long-term portion of notes payable | 2,029 | |||
Long-term portion of deferred revenue | 211,780 | |||
Other long-term liabilities | 215,000 | |||
| Total current and long-term liabilities | 1,880,984 | ||
Stockholders' Deficit | ||||
Common Stock, $.01 par value; 35,000,000 shares authorized; 23,929,388 shares outstanding | 239,294 | |||
Additional paid-in-capital | 25,624,347 | |||
Deficit accumulated during the development stage | (26,180,426) | |||
Treasury stock, at cost; 265,478 shares | (1,342,515) | |||
Total stockholders' deficit | (1,659,300) | |||
$ | 221,684 | |||
See accompanying notes to consolidated financial statements. |
(PAGE 3)
Paracelsian, Inc. and Subsidiary (A Development Stage Company) Consolidated Statements of Operations For the three months ended December 31, 2001 and 2000, and the cumulative period from inception to December 31, 2001 (Unaudited) | ||||||||
Three Months Ended | Cumulative Period from Inception to | |||||||
2001 | 2000 | 2001 | ||||||
Revenues: | ||||||||
Marketing rights - Ah-IMMUNOASSAY® | 92,103 | 63,255 | 1,084,069 | |||||
Products | 1,582 | 4,198 | 260,801 | |||||
Product testing | - | - | 169,977 | |||||
Product royalties | - | - | 1,246 | |||||
Subscription revenue | - | - | 31,625 | |||||
| Total Revenues | 93,685 | 67,453 | 1,547,718 | ||||
Operating expenses: | ||||||||
Research and product engineering | (37,788) | 122,945 | 9,416,290 | |||||
General and administrative | 180,525 | 257,646 | 16,021,267 | |||||
Product launch costs | - | - | 300,544 | |||||
Cost of products sold | 9,131 | 1,395 | 325,720 | |||||
Total Operating expenses | 151,868 | 381,986 | 26,063,821 | |||||
Loss from operations during the development stage | (58,183) | (314,533) | (24,516,103) | |||||
Other income | 9,000 | 9,000 | ||||||
Interest income (expenses) net | (11,215) | (186) | 428,801 | |||||
Gain on sale of assets | 1,348 | - | 25,876 | |||||
Net loss during the development stage | (59,050) | (314,719) | (24,052,426) | |||||
Basic and diluted net loss per share of common stock | (0.00) | (0.01) | ||||||
Weighted average number of Common Shares outstanding | 23,676,588 | 22,060,316 | ||||||
See accompanying notes to consolidated financial statements. |
(PAGE 4)
Paracelsian, Inc. and Subsidiary (A Development Stage Company) Consolidated Statements of Cash Flows For the three months ended December 31, 2001 and 2000, and the cumulative period from inception to December 31, 2001 (Unaudited) | ||||||||||
Cumulative | ||||||||||
Period from | ||||||||||
Three Months Ended | Inception to | |||||||||
December 31 , | December 31 , | |||||||||
2001 | 2000 | 2001 | ||||||||
Cash flows from operating activities: | ||||||||||
Net loss | (59,050) | (314,719) | (24,052,426) | |||||||
Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||||
Loss (gain) on the sale of assets | (1,348) | - | (25,876) | |||||||
Non-cash compensation expense | - | - | 1,619,657 | |||||||
Other non-cash expenses | (72,741) | - | 1,954,756 | |||||||
Depreciation and amortization | 10,253 | 20,774 | 2,420,601 | |||||||
Write-off of patents and trademarks | - | - | 160,363 | |||||||
Contributed capital | - | - | 80,000 | |||||||
Write-off of note and interest receivable | - | - | 359,965 | |||||||
Changes in assets and liabilities: | ||||||||||
Interest receivable | - | (9,845) | (62,465) | |||||||
Inventories | - | 926 | - | |||||||
Prepaid expenses and other current assets | (43,959) | (47,530) | (80,119) | |||||||
Accounts payable | (18,323) | 53,465 | 335,395 | |||||||
Deferred revenue and other long-term liabilities | 32,508 | - | 456,756 | |||||||
Accrued expenses | 17,389 | 71,369 | 710,380 | |||||||
Net cash used in operating activities: | (135,271) | (225,560) | (16,195,754) | |||||||
Cash flows from investing activities: | ||||||||||
Purchase of equipment | (1,464) | (3,805) | (742,182) | |||||||
Proceeds from sale of equipment | 1,348 | - | 39,176 | |||||||
Acquisition of licensed technology | - | - | (53,656) | |||||||
Acquisition of patents and trademarks | (16,615) | (3,282) | (524,099) | |||||||
Acquisition of New Century Nutrition newsletter | - | - | (350,000) | |||||||
Acquisition of option for East West Herbs, Ltd. and related acquisition costs | - | - | (92,866) | |||||||
Loan to East West Herbs, Ltd. | - | - | (340,000) | |||||||
Proceeds from loan to East West Herbs, Ltd. | - | - | 42,500 | |||||||
Net cash used in investing activities | (16,731) | (7,087) | (2,021,127) | |||||||
Cash flows from financing activities: | ||||||||||
Sale of common stock, initial public offering, net of costs | - | - | 5,124,014 | |||||||
Sale of common and preferred stock, net of costs | - | - | 11,776,088 | |||||||
Proceeds from the sale of common stock | - | - | 500,000 | |||||||
Proceeds from the exercise of warrants | - | - | 1,219,640 | |||||||
Proceeds from the exercise of options | - | - | 68,900 | |||||||
Purchase of treasury stock | - | - | (1,342,515) | |||||||
Cost of warrant dividend | - | - | (63,102) | |||||||
Increase in capital lease obligations and notes payable | - | - | 31,212 | |||||||
Payment on capital lease obligations | (96) | (4,240) | (29,792) | |||||||
Proceeds from advances from related party | - | - | 916,150 | |||||||
Payments on advances from related party | - | - | (105,473) | |||||||
Increase in notes payable | 6,490 | 44,791 | 139,097 | |||||||
Net cash provided by financing activities | 6,394 | 40,551 | 18,234,219 | |||||||
Net increase (decrease) in cash and cash equivalents | (145,608) | (192,096) | 17,338 | |||||||
Cash and cash equivalents, beginning of period | 162,946 | 227,123 | - | |||||||
Cash and cash equivalents, end of period | $ | 17,338 | 35,027 | 17,338 | ||||||
Supplemental disclosures: | ||||||||||
Cash paid during the period for interest | $ | 3,214 | 11,174 | 102,654 | ||||||
Supplemental disclosure of non-cash investing & financing activities: | ||||||||||
Fair value of assets acquired, net of cash acquired | $ | - | - | 1,733,212 | ||||||
Less - liabilities assumed | - | - | 83,212 | |||||||
Less - issuance of common stock | - | - | 1,644,000 | |||||||
Net cash paid | - | - | 6,000 | |||||||
Warrant dividend | - | - | 500,000 | |||||||
Issuance of common stock/warrants for services and to reduce liabilities | - | - | 1,599,788 | |||||||
Purchase of equipment | - | - | 90,950 | |||||||
Purchase of officer stock subscription receivable | - | - | 89,850 | |||||||
Issuance of common stock for licensing and technology rights | - | - | 3,338 | |||||||
See accompanying notes to consolidated financial statements |
(PAGE 5)
Paracelsian, Inc. and Subsidiary NOTES TO CONSOLIDATED FINANCIAL STATEMENTS 1. BASIS OF PRESENTATION: The unaudited consolidated financial statements included herein have been prepared in accordance with accounting principles generally accepted in the United States of America, pursuant to the rules and regulations of the Securities and Exchange Commission applicable to quarterly reporting on Form 10-QSB and reflect, in the opinion of the Company, all adjustments necessary to present fairly the financial position and results of operations for Paracelsian, Inc. and its consolidated subsidiary. All such adjustments are of a normal and recurring nature. The results of operations for the three month period ended December 31, 2001 are not necessarily indicative of the results to be expected for the full year. Certain information and footnote disclosures normally included in financial statements, prepared in accordance with unaudited accounting principles generally accepted in the United States of America, have been condensed or omitted as permitted by such regulations. These unaudited consolidated financial statements and related notes should be read in conjunction with the consolidated financial statements and related notes included in the Company's Annual Report on Form 10-KSB for the fiscal year ended September 30, 2001. (PAGE 6) 2. ORGANIZATION, BUSINESS, AND RISK FACTORS: Paracelsian is a development stage company, which develops and applies bioassays to monitor environmental toxins, to determine the quality of herbal products, and to identify therapeutic compounds from herbal sources (www.paracelsian.com). The Company has developed a highly sensitive, user friendly, cost effective testing system for the detection and quantification of highly toxic environmental chemicals generally known as dioxin and dioxin-like compounds. It is called the Ah-IMMUNOASSAY® Kit (AH-1 Method). Since the discovery of the dioxin compounds, during the late 1950’s, extensive research has been undertaken into their chemical and biological properties. And as more information becomes available, it is now clear that the original and narrowly defined group of ‘dioxins’ is becoming more expansive to include many other highly toxic, chemically similar compounds. Dioxin, although singular in name, is actually comprised of at least 17 chemical variants or congeners of a larger dioxin family. These chemicals are highly toxic, with the most active congener (TCDD) being the most toxic chemical ever discovered. The number of chemicals with dioxin-like activity is even much larger still than the 17 original polychlorodibenzo-p-dioxin (PCDD) families, such as the polychlorodibenzofurans (PCDF), the polychlorinated biphenyls (PCBs), the polybrominated biphenyls (PBBs), the polycyclic aromatic hydrocarbons (PAHs), the heterocyclic amines (HAs), among others. Probably no other group of chemicals has invoked more public health concern and received more media attention than these dioxin and dioxin-like substances, both because of their widespread distribution and their capability for serious toxicity (e.g., cancer, birth defects, diabetes, hormone disruption, immunologic dysfunction, etc.). The Environmental Protection Agency (EPA) of the United States has concluded, for example, that more than 100 of these dioxins and dioxin-like chemicals are likely human carcinogens. Waste incineration is a major source of these chemicals. Paper mill bleaching and varied industrial syntheses also add significant amounts to the environment. Following release into the air, perhaps also into waste water or sludge, these chemicals then settle on plant material, soil, and water where they are likely to persist for very long periods of time. As a consequence, they tend to accumulate either onto particulate matter (such as found at the bottom of bodies of water), or into body fat reservoirs of animals and fishes which feed on the plants. And because of their stability and persistence, these chemicals accumulate to relatively high levels in animal based foods. Investigating the distribution and toxicities of these chemicals has been challenging, both because of the ever-growing number of chemicals with dioxin-like activity and the difficulty of predicting toxicities. Because of these complexities, analysis of these chemicals has been very expensive, with the results being difficult to interpret. More recently, simpler analytical methods have been developed, such as the AH-1 Method, based on the use of biologically based concepts. Dioxins and dioxin-like chemicals (also called ligands), enter the cell and bind to a protein in the cytoplasm called Ah receptor (AhR), thus giving a ligand-AhR complex. This complex, by dropping and adding some smaller proteins (e.g., AhR translocator or ARNT, hsp-90 protein) is said to be ‘transformed’, thus enabling it to enter the nucleus to bind to a specific ‘dioxin receptor element’ (or enhancer) (DRE) of DNA. This interaction with DNA occurs ‘upstream’ of genes which then are activated to produce certain enzymes, some of which are highly correlated with the subsequent toxicity. The AH-I Method takes advantage of these facts. It is generally acknowledged, for example, that AhR binding appears to be essential for the development of toxicity by these chemicals. It is as if ligand binding of AhR is the main traffic intersection through which these chemicals pass on their way to produce their respective toxicities. In the AH-I Method, where an excess of AhR protein is provided, the amount of AhR-ligand complex that transforms is dependent on the amount of dioxin ligand present in the sample being assayed. The amount of the transformed complex is detected by using an antibody specific for the Ah-I protein component of the complex, thus giving the ‘Immunoassay’ name to the method. (For the scientifically minded reader, there really are two antibodies: the first interacts with the ARNT protein in the complex while the second, containing an enzyme that catalyzes the formation of the color reaction, binds to the first antibody. The color being produced in the reaction shows how much of the complex is present.). Dioxin is a toxic chemical group of widespread public health concern, and more information is needed, especially on the distribution of this material in the environment. More survey data are needed not only to identify potential ‘hot spots’ but also to allay unwarranted concerns. Until now, such survey work has been prohibitively expensive, but with the introduction of simpler and much more cost effective bioassay methods, such as the AH-1 Method, it is now possible to gather far more information in order to make wiser decisions. The herbal supplement market presents the opportunity to commercialize a quality assurance program that identifies the bioactivity present in herbal products, which are complex mixtures of substances. This product is a significant advance versus current practices for verifying the quality and the bioactivity of herbal products. This is the Company’s BioFIT™ Quality Assurance Certification Program. Typically, the Company will investigate the effect of a compound or mixture of compounds on a disease (such as cancer) or a symptom (such as depression). The Company scientists conduct in depth research of the scientific literature and review the results of successful clinical trials to establish the best scientific explanation for the positive results seen in such trials. Based on their review, they identify the biological mechanism which, if activated, would best explain the positive clinical results. By defining such mechanisms of action associated with a wide variety of biological effects the Company scientists can then test a wide variety of natural materials in "in vitro" models which demonstrate these effects for the purpose of either discovering or confirming these biological activities. Such discovery or confirmation provides the Company with the basis for its BioFIT™ Program. The Company is continuing to work with its Chinese colleagues, during the appropriate market conditions, to expand the scope of the BioFIT™ program to the rest of the world. The Company is engaged in an internet-based health exchange between the US and China and currently maintains the website www.newcenturynutrition.com. The Company has excellent relations with recognized health authorities and organizations within the People’s Republic of China. This website serves to provide a forum for the exchange of nutrition, health and related information. At its core is the New Century Nutrition website where renowned researchers, teachers and physicians from both countries can discuss their philosophies, research findings and health advice. Other components of the site include an herbal resource center featuring herbal databases from China, a nutrition resource center featuring healthy recipes and a technology center featuring the Ah-IMMUNOASSAY® Kit and the BioFIT™ Program. Our goal is to combine the best of Chinese medical practice with the best of Western practice creating new opportunities for information on health and disease prevention. The Company has a 10 year agreement with Kubota Corporation (Kubota) of Japan that establishes Kubota as the exclusive marketing and distribution agent for Paracelsian's Ah-IMMUNOASSAY® Environmental Certification program in Japan. For the period ended December 31, 2001, the Company recognized approximately $7,500 in license revenue under this agreement. The Company has a License Revocation Agreement with Dow Chemical Company (DOW) that modified the entirety of the License Agreement dated January 19, 1995. Under the agreement the Company agreed to pay DOW 10% of all sublicense fees of the proprietary information which formed the basis of the License Agreement and 10% of any sales of any products derived from the proprietary information which are the subject of the License Agreement. The maximum total value for any and all such payments shall not exceed $250,000. As of December 31, 2001, $66,675 has been accrued as payments under this agreement. The Company has signed an Exclusive License Agreement with the Cornell Research Foundation, Inc. (CRF) for the exclusive license to make, have made, use or sell Licensed Products throughout the world. This agreement pertains to the manufacture and sales of Paracelsian's Ah-IMMUNOASSAY® Kits. This agreement stipulates that Paracelsian will pay to CRF a royalty of 3% of any sales of the Kits. As of December 31, 2001, $15,502 has been accrued as royalty payments. The Agreement also states that the Company shall reimburse CRF for any patent costs incurred by CRF associated with the Licensed Products. The Company has accrued $64,928 for patent expenses. Development Stage Company and Risk Factors The Company is considered to be a development stage company as defined in Statement of Financial Accounting Standards No. 7, "Accounting and Reporting by Development Stage Enterprises." Since inception, the Company has been primarily engaged in research, product engineering and raising capital. The Company, as a development stage enterprise, has yet to generate significant revenues and has no assurance of substantial future revenues. The Company is subject to a number of risks that may affect its ability to become an operating enterprise or impact its ability to remain in existence, including risks related to successful development and marketing of its products, patent protection of proprietary technology, government regulation, competition from substitute products (including technologies that may not yet have been developed), dependence on key employees and the need to obtain additional funds that may not be available to it. As shown in the accompanying financial statements, the Company incurred a net loss of approximately $59,000 for the three months ended December 31, 2001 and had a working capital deficit of approximately $1,354,000. Operating expenses decreased by approximately $230,000 (73%) from the prior year first quarter as a result of decreases in a variety of expenses including salaries, office expense, consultant fees and depreciation and amortization, as part of the company’s program to control costs and optimize the use of its resources and due to a change in accounting estimate of approximately $73,000 related to reimbursement of patent costs by Cornell Research Foundation, Inc. Management believes that revenues from its Ah-IMMUNOASSAY® will increase throughout the year and will enable the Company to achieve positive cash flow. In December 2001, the Company made an offer to acquire the assets of East West Herbs (USA) in exchange for the note receivable and accrued interest owed to the Company. The offer was accepted and the parties are in the process of preparing an Asset Purchase Agreement. Management is seeking an investment of at least $1 million to strengthen its working capital position, and active discussions with interested parties are continuing. Current monthly cash requirements in order to sustain meaningful operations are approximately $80,000. Management will continue to evaluate the most cost effective means of raising any needed capital. Although management is confident of its ability to raise the capital, there can be no assurance that additional financing will be available on acceptable terms or at all. ITEM 2. Management's Discussion and Analysis of Financial Condition and Results of Operations As a development stage enterprise, the Company, since inception, has been primarily engaged in research, product engineering, and capital formation. As such, the Company has not generated significant revenues to date on a recurring basis. The Company signed a final Licensing Agreement on January 21, 2000 with Kubota Corporation for the sale of Paracelsian’s Ah-IMMUNOASSAY® in the Japanese market and began manufacturing and selling kits to Kubota. This 'bioassay' based kit is rugged, user-friendly, portable, analytically sensitive, and low cost when compared with the existing methodology. The agreement with Kubota will provide revenues from the sale of kits and royalties. On June 15, 2000 the Company announced that in accordance with the License Agreement, Kubota agreed to pay the initial $150,000 License Fee. The License Agreement also calls for a second payment of $150,000 within (30) days of the third anniversary of the Agreement. Kubota after using and evaluating the Ah-IMMUNOASSAY® Kits concluded that the methodology is effective for their purposes, and Kubota paid the $150,000 on August 8, 2001, seventeen months sooner. On October 1, 2001 Kubota and the Company announced an agreement where Kubota will pay the Company $350,000, earmarked for upgrading the Ah-IMMUNOASSAY® Kits. The first payment of $175,000 was made in September 2001 and the second payment of $40,000 was made in December 2001. The third payment of $90,000 will be made in March 2002 and the fourth and final payment of $45,000 will be made in September 2002. Under the terms of the agreement, the Company is required to compensate Kubota beginning in January 2003 based on sales of the Ah-IMMUNOASSAY® Kits. The Company has accounted for the proceeds under the agreement as other long-term liabilities. Results of Operations The Company's net loss for the first quarter of fiscal 2002 was approximately $59,000 compared to approximately $315,000 in the first quarter of fiscal 2001. Revenues for the three-month period were approximately approximately $94,000 in 2002 as compared to approximately 67,000 in 2001. The $27,000 increase in revenues is attributable to revenues for the Ah-IMMUNOASSAY® Kits. Operating expenses for the three-month period were approximately $152,000 compared to approximately $382,000 for the first fiscal quarter of the prior year. The decrease of approximately $230,000 (60%) is due to a decrease in a number of expense categories including payroll, office expense, consultant fees, depreciation and amortization and a change in accounting estimate of approximately $73,000. The management team is continuing to operate with modest staff levels and has been focusing on continuing to optimize its resources, increasing its customer base and generating revenues. (PAGE 9) Liquidity & Capital Resources As of December 31, 2001, the Company had cash of $17,338 and a net working capital deficit of $1,354,000. Management believes that it can continue to raise additional capital to support its operations until such time as the revenue stream is sufficient to realize positive cash flow. Management believes that the additional financing coupled with its expected revenues from the Ah-IMMUNOASSAY® will enable the Company to increase sales, to further improve its operating efficiency and to continue its operations into the future. In January and February 2001 the Company issued three Convertible Promissory Agreements in the amounts of $50,000, $30,000 and $10,000. The Agreements mature in one year from the issuance date and each holder may convert the Agreement into shares of Restricted Common Stock of the Company at any time up to and including the maturity date but not thereafter. The $50,000 Agreement expired on February 15, 2002 and was extended to August 15, 2002. The $30,000 Agreement expired on January 10, 2002 and was extended to July 10, 2002 and the $10,000 Agreement expired on January 9, 2002 and was extended to July 9, 2002. In December 2001, the Company made an offer to acquire the assets of East West Herbs (USA) in exchange for the note receivable and accrued interest owed to the Company. The offer was accepted and the parties are in the process of preparing an Asset Purchase Agreement. Management is seeking an investment of at least $1 million to strengthen its working capital position, and active discussions with interested parties are continuing. Current monthly cash requirements in order to sustain meaningful operations are approximately $80,000. Management will continue to evaluate the most cost effective means of raising any needed capital. Although management is confident of its ability to raise the capital, there can be no assurance that additional financing will be available on acceptable terms or at all. Management and The Board The management of the Company will be focusing their efforts on growing its customer base, producing ongoing revenues and controlling expenses. On November 13, 2001 Mac Shaibe resigned from the Board. The Board is pursuing a replacement for Mr. Shaibe. Short-Term Advances BioSignia, Inc., the Company's largest shareholder, has advanced interim funds to the Company for working capital purposes. The Company agrees to repay the funds, together with quarterly interest at an annual rate of prime plus 2% and its obligation to satisfy the indebtedness matures on September 1, 2002. Through December 31, 2001 $348,885 has been advanced, including accrued interest. Forward Looking Statements Certain statements in this Form 10-QSB "Management's Discussion and Analysis of Financial Condition and Results of Operations" constitute "forward looking statements" within the meaning of the Private Securities Litigation Reform act of 1995. Such forward looking statements involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of the Company to be materially different from any future results, performance or achievements expressed or implied by such forward looking statements. Such factors include, among others, the following: success of operating initiative, advertising and promotional efforts, acceptance of new product offerings, availability, changes in business strategy or development plan, availability and terms of capital, labor and employee benefit costs, and other factors specifically referred to in this 10-QSB. PART II OTHER INFORMATION Item 1. Legal Proceedings Hadyk, et al. V. John G. Babish, et al. In addition to routine litigation that is incidental to its business, the Company is a party to the following litigation: (PAGE 10) Hadyk, et al. V. John G. Babish, et al.: This case was commenced in New York State Supreme Court (Onondaga County) in June 1993 by certain persons, individually and doing business as In Vitro Bioanalytic Systems, against the Company, Dr. John G. Babish, a former officer and director of the Company, and Edward Heslop, a founding shareholder of the Company, primarily as an action for money damages and injunctive relief against the Company for alleged misappropriation of proprietary information and unfair competition. The plaintiffs allege, among other things, that in 1990, prior to the Company's incorporation, a partnership has been formed with Messrs. Babish and Heslop to commercialize products that the Company was developing. Damages, an accounting and an injunction are being sought against the Company. By decision dated September 14, 1994, the Court dismissed certain of the plaintiff’s claims against the Company while permitting a claim alleging unfair competition to proceed. Discovery has been temporarily stayed pending resolution of a motion for summary judgment brought by certain of the Company's co-defendants. That motion was successfully and fully resolved, and the Judge, on March 7, 2001 signed an order dismissing all of the plaintiff’s refining claims against the Company. In December 2001, the plaintiffs filed an appeal. The Company intends to be fully responsive to the appeal and is confident of the summary judgment motion being upheld. Item 6(a) Exhibits None Item 6(b) Reports on Form 8-K None SIGNATURES In accordance with Section 13 or 15 (d) of the Securities and Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized. Date February 15, 2002 PARACELSIAN, INC.
PARACELSIAN, INC. By:/s/ NoriYoshi Inoue By/s/ GARY G. CHABOT
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