SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

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

For the quarterly period ended JuneSeptember 30, 2014

OR

oTRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from               to

Commission file number:  000-55158

COCRYSTAL PHARMA, INC.
(Exact Name of Registrant as Specified in Its Charter)

Delaware 20-578559
(State or Other Jurisdiction of Incorporation or Organization) (I.R.S. Employer Identification No.)
   
19805 North Creek Parkway  
Bothell, Washington 98011
(Address of Principal Executive Offices) (Zip Code)

(425) 398-7178
(Registrant’s Telephone Number, Including Area Code)
 
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. Yes  x   No  o
 
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).  Yes  x   No  o

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act. (Check one):

Large accelerated filer   oAccelerated filer  o
    
Non-accelerated filer   oSmaller reporting company  x
(Do not check if a smaller reporting company)   

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes  o  No  x

As of August 8,November 14, 2014, the number of outstanding shares of the registrant’s common stock, par value $0.001 per share, was 121,959,404.122,493,690. 




 
 




COCRYSTAL PHARMA, INC.
 
FORM 10-Q FOR THE QUARTER ENDED JUNESEPTEMBER 30, 2014

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-i-


PaPart Irt I – FINANCIAL INFORMATION
Cocrystal Pharma, Inc.
CONDENSED CONSOLIDATED BALANCBALANCE SHEETSE SHEETS
(in thousands)
 
  
June 30,
2014
  
December 31,
2013
 
  (unaudited)    
Assets      
Current assets:      
Cash and cash equivalents $4,074  $1,034 
Marketable securities  5,719   - 
Prepaid and other current assets  156   139 
Mortgage note receivable, current portion  148   - 
Total current assets  10,097   1,173 
         
Property and equipment, net  361   469 
Deposits  31   19 
Mortgage note receivable, long-term portion  2,478   - 
Total assets $12,967  $1,661 
         
Liabilities and stockholders' equity (deficit)        
Current liabilities:        
Accounts payable  180   224 
Accrued expenses  281   139 
Derivative liabilities  6,450   23 
Total current liabilities  6,911   386 
Total liabilities  6,911   386 
         
Commitments and contingencies        
Series A convertible preferred stock, $0.001 par value; 7,150 shares authorized; 0 and 7,046 shares issued and outstanding at June 30, 2014 and December 31, 2013, respectively; liquidation preference of $14,000 as of December 31, 2013  -   10,108 
         
Stockholders' equity (deficit):        
Series B convertible preferred stock, $.001 par value; 5,000 shares authorized; 1,000 and 279 shares issued and outstanding at June 30, 2014 and December 31, 2013, respectively  1   - 
Common stock, $.001 par value; 200,000 and 262,186 shares authorized, 121,885 and 0 shares issued and outstanding as of June 30, 2014 and December 31, 2013, respectively  122   - 
Additional paid-in capital  12,084   3,502 
Accumulated other comprehensive income  1,827   - 
Accumulated deficit  (7,978)  (12,335
Total stockholders' equity (deficit)  6,056   (8,833)
         
Total liabilities and stockholders' equity (deficit) $12,967  $1,661 

  September 30, 2014  December 31, 2013 
  (unaudited)    
Assets      
Current assets:      
Cash and cash equivalents $3,006  $1,034 
Marketable securities  2,500   - 
Prepaid and other current assets  116   139 
Mortgage note receivable, current portion  181   - 
Total current assets  5,803   1,173 
         
Property and equipment, net  314   469 
Marketable securities, long-term portion  3,043     
Deposits  22   19 
Mortgage note receivable, long-term portion  2,453   - 
Total assets $11,635  $1,661 
         
Liabilities and stockholders' equity (deficit)        
Current liabilities:        
Accounts payable  125   224 
Accrued expenses  290   139 
Derivative liabilities  7,242   23 
Total current liabilities  7,657   386 
Total liabilities  7,657   386 
         
Commitments and contingencies        
Series A convertible preferred stock, $0.001 par value; 7,150 shares authorized; 0 and 7,046 shares issued and outstanding at September 30, 2014 and December 31, 2013, respectively; liquidation preference of $14,000 as of December 31, 2013  -   10,108 
         
Stockholders' equity (deficit):        
Series B convertible preferred stock, $.001 par value; 5,000 shares authorized; 1,000 and 279 shares issued and outstanding at September 30, 2014 and December 31, 2013, respectively  1   - 
Common stock, $.001 par value; 200,000 and 262,186 shares authorized, 122,494 and 0 shares issued and outstanding as of September 30, 2014 and December 31, 2013, respectively  123   - 
Additional paid-in capital  12,146   3,502 
Accumulated other comprehensive income  2,235   - 
Accumulated deficit  (10,527)  (12,335)
Total stockholders' equity (deficit)  3,978   (8,833)
         
Total liabilities and stockholders' equity (deficit) $11,635  $1,661 
 
F-1


 
Cocrystal Pharma, Inc.
CONDENSED CONSOLIDATED STATEMENTSSTATEMENTS OF COMPREHENSIVE INCOME (LOSS)
(unaudited)
(in thousands)
 
 Three months ended June 30,  Six months ended June 30,  
Three months ended
September 30,
  
Nine months ended
September 30,
 
 2014  2013  2014  2013  2014  2013  2014  2013 
                        
Operating expenses                        
Research and development $888  $980  $1,853  $1,986  $866  $950  $2,722  $2,936 
General and administrative  499   51   1,066   104   353   55   1,417   159 
Total operating expenses  1,387   1,031   2,919   2,090   1,219   1,005   4,139   3,095 
                                
Loss from operations  (1,387)  (1,031)  (2,919)  (2,090)  (1,219)  (1,005)  (4,139)  (3,095)
                                
Interest income  -   1   -   2   50   -   50   2 
Realized gain on sale of marketable securities  480   -   480   -   -   -   480   - 
Other expense  (2)  -   (2)  -   (4)  -   (5)  - 
Fair value of warrant liabilities in excess of proceeds from financing  -   -   (946)  -   -   -   (946)  - 
Loss on return of escrowed shares, net  (584)  -   (584)  - 
Change in fair value of derivative liabilities  5,639   -   7,744   -   (792)  -   6,952   - 
Total other income, net  6,117   1   7,276   2 
Total other income (expense), net  (1,330)  -   5,947   2 
                                
Income (loss) before income taxes  4,730   (1,030)  4,357   (2,088)  (2,549)  (1,005)  1,808   (3,093)
                                
Income taxes  -   -   -   -   -   -   -   - 
                                
Net income (loss) $4,730  $(1,030) $4,357  $(2,088) $(2,549) $(1,005) $1,808  $(3,093)
                                
Comprehensive income (loss):                                
Net income (loss) $4,730  $(1,030) $4,357  $(2,088) $(2,549) $(1,005) $1,808  $(3,093)
Unrealized gain on marketable securities  3,354   -   1,827   -   408   -   2,235   - 
Total comprehensive income (loss) $8,084  $(1,030) $6,184  $(2,088) $(2,141) $(1,005) $4,043  $(3,093)
                                
Net income (loss) per common share:                                
Basic income (loss) per share $0.01  $(0.02) $0.01  $(0.04)
Weighted average common shares outstanding, basic  326,760   57,255   326,160   57,255 
Diluted loss per share $(0.00) $(0.02) $(0.01) $(0.04)
Weighted average common shares outstanding, diluted  326,760   57,255   326,160   57,255 
Net income (loss) per share, basic $(0.01) $(0.02) $0.01  $(0.05)
Net loss per share, diluted $(0.01) $(0.02 $(0.02 $(0.05
Weighted average common shares outstanding, basic and diluted  327,209   57,255   326,534   57,255 

 
F-2



Cocrystal Pharma, Inc.
CONDENSED CONSOLIDATED STATEMENTS OF CONVERTIBLE PREFERRED PREFERRED STOCK AND STOCKHOLDERS' EQUITY (DEFICIT)
(unaudited)
(in thousands)
 
 Series A Convertible Preferred Stock  Series B Convertible Preferred Stock  Common Stock  Additional Paid-in Capital  Accumulated other comprehensive income  Accumulated deficit  Total Stockholders' Equity (Deficit)  Series A Convertible Preferred Stock  Series B Convertible Preferred Stock  Common Stock  Additional Paid-in Capital  Accumulated other comprehensive income  Accumulated deficit  Total Stockholders' Equity (Deficit) 
 Shares  Amount  Shares  Amount  Shares  Amount              Shares  Amount  Shares  Amount  Shares  Amount             
Balance as of December 31, 2013  7,046  $10,108   279  $-     $-  $3,502  $-  $(12,335) $(8,833)  7,046  $10,108   279  $-   -  $-  $3,502  $-  $(12,335) $(8,833)
Conversion of series A convertible stock  (7,046)  (10,108)  721   1   -   -   10,107   -   -   10,108   (7,046)  (10,108)  721   1   -   -   10,107   -   -   10,108 
Merger between Biozone Pharmaceuticals, Inc. and Cocrystal Discovery, Inc.  -   -   -   -   115,907   116   (1,596)  -   -   (1,480)  -   -   -   -   115,907   116   (1,596)  -   -   (1,480)
Exercise of common stock options  -   -   -   -   478   -   57   -   -   57   -   -   -   -   1,087   1   114   -   -   115 
Stock-based compensation  -   -   -   -   -   -   20   -   -   20   -   -   -   -   -   -   25   -   -   25 
Issuance of common stock and warrants in January 2014  -   -   -       5,500   6   (6)  -   -   -   -   -   -   -   5,500   6   (6)  -   -   - 
Unrealized gain on marketable securities  -   -   -   -   -   -   -   1,827   -   1,827   -   -   -   -   -   -   -   2,235   -   2,235 
Net income  -   -   -   -   -   -   -   -   4,357   4,357   -   -   -   -   -   -   -   -   1,808   1,808 
                                                                                
Balance as of June 30, 2014  -  $-   1,000  $1   121,885  $122  $12,084  $1,827  $(7,978) $6,056 
Balance as of September 30, 2014  -  $-   1,000  $1   122,494  $123  $12,146  $2,235  $(10,527) $3,978 


 
F-3


Cocrystal Pharma, Inc.
CONDENSED CONSOLIDATED STATEMENTS STATEMENTS OF CASH FLOWS
(unaudited)
(in thousands)
 
 Nine months ended September 30, 
 Six months ended June,  2014  2013 
 2014  2013       
Operating activities:            
Net income (loss) $4,357  $(2,088) $1,808  $(3,093)
Adjustments to reconcile net income (loss) to net cash used in operating activities:        Adjustments to reconcile net income (loss) to net cash used in operating activities:     
Depreciation  107   119   154   178 
Stock-based compensation  20   31   25   43 
Fair value of warrant liabilities in excess of proceeds from financing  946   -   946   - 
Change in fair value of derivative liabilities  (7,744)  -   (6,952)  - 
Loss on return of escrowed shares, net  584   - 
Realized gain on sale of marketable securities  (480)  -   (480)  - 
Loss on sale of equipment  2   -   6   - 
Interest receivable  (16)    
Changes in operating assets and liabilities, net of effects of reverse merger with Biozone Pharmaceuticals, Inc.:        Changes in operating assets and liabilities, net of effects of reverse merger with Biozone Pharmaceuticals, Inc.: 
Prepaid expenses and other current assets  (14)  41   26   39 
Accounts payable and accrued expenses  (312)  (33)  (358)  (45)
Net cash used in operating activities  (3,118)  (1,930)  (4,257)  (2,878)
                
Investment activities:                
Cash acquired in reverse merger with Biozone Pharmaceuticals, Inc.  589   - 
Cash acquired in acquisition of Biozone Pharmaceuticals, Inc.  589   - 
Purchase of fixed assets  (4)  (1)
Long term deposits  (12)  -   (3)  - 
Proceeds from sale of marketable securities  5,400   -   5,400   - 
Investment in mortgage note receivable  (2,626)  -   (2,626)  - 
Net cash provided by investing activities  3,351   - 
Principal payments received on mortgage note receivable  8   - 
Net cash provided by (used in) investing activities  3,364   (1)
                
Financing activities        
Financing activitities        
Proceeds from exercise of stock options  57   5   115   5 
Proceeds from issuance of common stock and warrants  2,750   -   2,750   - 
Net cash provided by financing activities  2,807   5   2,865   5 
                
Net increase (decrease) in cash and cash equivalents  3,040   (1,925)  1,972   (2,874)
Cash and cash equivalents at beginning of period  1,034   4,717   1,034   4,717 
Cash and cash equivalents at end of period $4,074  $2,792  $3,006  $1,843 
                
SUPPLEMENTAL DISCLOSURE OF NON-CASH INVESTING AND FINANCING ACTIVITIES:SUPPLEMENTAL DISCLOSURE OF NON-CASH INVESTING AND FINANCING ACTIVITIES:     SUPPLEMENTAL DISCLOSURE OF NON-CASH INVESTING AND FINANCING ACTIVITIES:    
Unrealized gain on marketable securities $1,827  $-  $2,235  $- 
Fair value of assets acquired and liabilities assumed in reverse merger with Biozone Pharmaceuticals, Inc.        Fair value of assets acquired and liabilities assumed in reverse merger with Biozone Pharmaceuticals, Inc. 
Prepaid expenses and other current assets $3  $-  $3  $- 
Marketable securities  8,811   -   8,811   - 
Accounts payable and accrued expenses  410   -   410   - 
Derivative liabilities  10,475   -   10,475   - 


 
F-4


 Cocrystal Pharma, Inc.
Notes to the Condensed ConsolidatedConsolidated Financial Statements
JuneSeptember 30, 2014
(unaudited)

Note 1- Organization and Significant Accounting Policies

Overview
 
On January 2, 2014, Biozone Pharmaceuticals, Inc. merged with Cocrystal Discovery, Inc (as further described below).  The Company was previously incorporated in Nevada under the name Biozone Pharmaceuticals, Inc. ("Biozone"). On March 18, 2014, the Company reincorporated in Delaware under the name Cocrystal Pharma, Inc. ("we", the "Company", or "Cocrystal").
 
Our primary business going forward is to develop novel medicines for use in the treatment of human viral diseases.  Cocrystal has been developing novel technologies and approaches to create first-in-class and best-in-class antiviral drug candidates since its initial funding in 2008. Subsequent funding was provided to Cocrystal Discovery, Inc. ("Cocrystal Discovery") by Teva Pharmaceuticals Industries, Ltd., or Teva, in 2011.  Our focus is to pursue the development and commercialization of broad-spectrum antiviral drug candidates that will transform the treatment and prophylaxis of viral diseases in humans. By concentrating our research and development efforts on viral replication inhibitors, we plan to leverage our infrastructure and expertise in these areas.
 
Effective January 2, 2014, Biozone, Biozone Acquisitions Co., Inc., a wholly-owned subsidiary of Biozone (the “Merger Sub”), and Cocrystal Discovery entered into and closed an Agreement and Plan of Merger (the “Merger Agreement”). Pursuant to the Merger Agreement, Merger Sub merged with and into Cocrystal Discovery (the “Merger”), with Cocrystal Discovery continuing as the surviving corporation and a wholly-owned subsidiary of Biozone. Cocrystal Discovery is considered the accounting acquirer as its shareholders own 60% of the combined entity after the Merger. In connection with the Merger agreement, all of the Company’s shares of Series A preferred stock were first converted to common stock, and Biozone then issued to Cocrystal Discovery’s security holders a total of 1,000,000 shares of the Company’s Series B Convertible Preferred Stock (“Series B”) (at a ratio of 0.07454 Series B stock for each common share of Cocrystal Discovery). The Series B shares: (i) automatically convert into shares of the Company’s common stock at a rate of 205.08308640 shares for each share of Series B at such time that the Company has sufficient authorized capital, (ii) are entitled to vote on all matters submitted to shareholders of the Company and vote on an as converted basis and (iii) have a nominal liquidation preference. Additionally, the Company assumed all of the outstanding stock options under the Cocrystal Discovery 2007 Equity Incentive Plan. Subsequent to the Merger, Biozone changed its name to Cocrystal Pharma, Inc.
 
The Merger is being treated as a reverse merger and recapitalization effected by a share exchange for financial accounting and reporting purposes since substantially all of Biozone’s operations were disposed of immediately prior to the consummation of the Merger as reported on a Form 8-K filed by Biozone on January 2, 2014. Cocrystal Discovery is treated as the accounting acquirer as its shareholders control the Company after the Merger, even though Biozone was the legal acquirer. As a result, the assets and liabilities and the historical operations that are reflected in these financial statements are those of Cocrystal Discovery as if Cocrystal Discovery had always been the reporting company and, on the Merger date, changed its name and reorganized its capital stock. Since Biozone had no operations upon the Merger taking place, the transaction was treated as a recapitalization for accounting purposes and no goodwill or other intangible assets were recorded by the Company as a result of the Merger.  Historical common stock amounts and additional paid-in capital have been retroactively adjusted using the exchange ratio of 0.07454 Series B shares for each one common share of Cocrystal Discovery.
 
The Company’s activities since inception have consisted principally of acquiring product and technology rights, raising capital, and performing research and development. Successful completion of the Company’s development programs and, ultimately, the attainment of profitable operations are dependent on future events, including, among other things, its ability to access potential markets; secure financing; develop a customer base; attract, retain and motivate qualified personnel; and develop strategic alliances. Through JuneSeptember 30, 2014, the Company has funded its operations through equity offerings, private placements of convertible debt and debt financings.

 
F-5


As of JuneSeptember 30, 2014, the Company had an accumulated deficit of $8.0$10.5 million. During the three month period ended JuneSeptember 30, 2014, the Company had a loss from operations of $1.4$1.2 million. During the sixnine month period ended JuneSeptember 30, 2014, the Company had a loss from operations of $2.9$4.1 million. Cash used in operating activities was approximately $3.1$4.2 million for the sixnine months ended JuneSeptember 30, 2014. The Company expects to continue to incur substantial operating losses and negative cash flows from operations over the next several years during its clinical development phase.
 
F-5

In addition to the Company’s cash balance of $4,074,000$3,006,000 as of JuneSeptember 30, 2014, the Company owns 600,000510,000 shares of MusclePharm, Inc. (“MusclePharm”) common stock, as further discussed in Note 7. The 510,000 shares were part of 600,000 shares areoriginally issued to the Company related to the Company’s sale of assets to MusclePharm that were required to be held in escrow until October 2014 to satisfy any breaches of representations under the Merger Agreement.  On September 29, 2014, the Company signed a Memo of Understanding in which it agreed to release 90,000 shares of MusclePharm stock out of the original balance of 600,000 shares held in escrow in exchange for a release from all claims which MusclePharm had made concerning assets which it acquired in its purchase of assets from the Company in January 2014. The Company is uncertain whetherrecognized a net loss on the return of these MusclePharm shares of $584,000 in the three months ended September 30, 2014.  MusclePharm did not withdraw the portion of its claim that relates to the pending eviction proceedingproceedings described in Note 11 below and will be used bycontinue to hold in escrow 260,000 shares of its stock pending such time as MusclePharm to delay delivery of the shares from escrow. Unlessand the Company is ablecan reach a mutually agreeable arrangement with respect to sell the MusclePharm lease.  In October 2014, MusclePharm exercised its right to repurchase 250,000 shares of MusclePharm shares at $10.00 per share.  Based on the $3,006,000 cash on hand and the receipt of the $2,500,000 from MusclePharm from the repurchase of its shares subsequent to September 30, 2014, the Company believes that it does not havehas sufficient cash to fund its current operating plan for at least the next 12 months.  As the Company continues to incur losses, achieving profitability is dependent upon the successful development, approval and commercialization of its product candidates, which is a number of years in the future. Once that occurs, it will have to achieve a level of revenues adequate to support its cost structure. The Company may never achieve profitability, and unless and until it does, it will continue to need to raise additional capital. The Company intends to fund future operations through additional private or public debt or equity offerings, and may seek additional capital through arrangements with strategic partners or from other sources. In addition it may, if appropriate or necessary, sell the MusclePharm common stock, if released from escrow. There can be no assurances, however, that additional funding will be available on terms acceptable to the Company, or at all.  Failure to generate revenue or raise additional capital would adversely affect the Company’s ability to achieve its intended business objectives.

Basis of Presentation and Significant Accounting Policies

The accompanying condensed consolidated financial statements have been prepared pursuant to the rules of the Securities and Exchange Commission ("SEC"). Certain information and footnote disclosures, normally included in annual financial statements prepared in accordance with U.S. generally accepted accounting principles ("GAAP"), have been condensed or omitted pursuant to those rules and regulations. We believe disclosures made are adequate to make the information presented not misleading. In the opinion of management, all adjustments, consisting only of normal recurring adjustments necessary to fairly state the financial position, results of operations and cash flows with respect to the interim condensed consolidated financial statements have been included.  The results of operations for the interim periods are not necessarily indicative of the results of operations for the entire fiscal year. All intercompany accounts and transactions have been eliminated in consolidation. Reference is made to the audited annual financial statements of Cocrystal Discovery, Inc. included in our Form 8-K/A filed with the SEC on March 20, 2014 (“Form 8-K/A”) and the Annual Report on Form 10-K/A for the year ended December 31, 2013 of Biozone Pharmaceuticals, Inc. filed on April 4, 2014 (“Annual Report”) which contain information useful to understanding the Company's businesses and financial statement presentations. The Condensed Consolidated Balance Sheet as of December 31, 2013 was derived from the Company's most recent audited financial statements, but does not include all disclosures required by GAAP for a year-end balance sheet. Our significant accounting policies and practices are presented in Note 2 to the financial statements included in the Form 10-Q/10-K/A.
 
Use of Estimates
 
The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting period. Actual results could differ from those estimates.
 
F-6


Recent Accounting Pronouncements

In June 2014, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) No. 2014-10, Development Stage Entities: Elimination of Certain Financial Reporting Requirements, Including an Amendment to Variable Interest Entities Guidance in Topic 810, Consolidation, which eliminates the concept of a development stage entity, or DSE, in its entirety from GAAP. Under previous guidance, DSEs were required to report incremental information, including inception-to-date financial information, in their financial statements. A DSE is an entity devoting substantially all of its efforts to establishing a new business and for which either planned principal operations have not yet commenced or have commenced but there has been no significant revenues generated from that business. Entities classified as DSEs are no longer subject to these incremental reporting requirements after adopting ASU No. 2014-10. ASU No. 2014-10 is effective for fiscal years beginning after December 15, 2014, with early adoption permitted. Prior to the issuance of ASU No. 2014-10, the Company had met the definition of a DSE since its inception. The Company elected to adopt this ASU early, and therefore it has eliminated the incremental disclosures previously required of DSEs, starting with this Quarterly Report on Form 10-Q.DSEs.
F-6


In August 2014, the FASB issued ASU No. 2014-15, Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern (ASU 2014-15). ASU 2014-15 requires management to determine whether substantial doubt exists regarding the entity’s going concern presumption, which generally refers to an entity’s ability to meet its obligations as they become due. If substantial doubt exists but is not alleviated by management’s plan, the footnotes must specifically state that “there is substantial doubt about the entity’s ability to continue as a going concern within one year after the financial statements are issued”. In addition, if substantial doubt exists, regardless of whether such doubt was alleviated, entities must disclose (a) principal conditions or events that raise substantial doubt about the entity’s ability to continue as a going concern (before consideration of management’s plans, if any); (b) management’s evaluation of the significance of those conditions or events in relation to the entity’s ability to meet its obligations; and (c) management’s plans that are intended to mitigate the conditions or events that raise substantial doubt, or that did alleviate substantial doubt, about the entity’s ability to continue as a going concern. If substantial doubt has not been alleviated, these disclosures should become more extensive in subsequent reporting periods as additional information becomes available. In the period that substantial doubt no longer exists (before or after considering management’s plans), management should disclose how the principal conditions and events that originally gave rise to substantial doubt have been resolved. The ASU applies prospectively to all entities for annual periods ending after December 15, 2016, and to annual and interim periods thereafter. Early adoption is permitted. The Company has not adopted the provisions of this ASU.
Note 2 – Fair Value Measurements

The companyCompany follows FASB Accounting Standards Codification (“ASC”) 820, “Fair Value Measurements and Disclosures,” (“ASC 820”) for the company’sCompany’s financial assets and liabilities that are re-measured and reported at fair value at each reporting period, and are re-measured and reported at fair value at least annually using a fair value hierarchy that is broken down into three levels. Level inputs are as defined as follows:
 
Level 1 — quoted prices in active markets for identical assets or liabilities.
Level 2 — other significant observable inputs for the assets or liabilities through corroboration with market data at the measurement date.
Level 3 — significant unobservable inputs that reflect management’s best estimate of what market participants would use to price the assets or liabilities at the measurement date.
 
The companyCompany categorized its cash equivalents as Level 1 fair value measurements. As further discussed in Note 87 below, certain of the Company’s marketable securities are subject to restrictions on sale and an option for the issuer to repurchase those shares from the Company as of JuneSeptember 30, 2014. The fair value of these marketable securities is therefore considered to be a Level 2 fair value measurement. The valuation for Level 1 financial instruments was determined based on a “market approach” using quoted prices in active markets for identical assets. Valuations of these assets do not require a significant degree of judgment. The valuation for the 260,000 marketable securities categorized as Level 2 was based on applying a discount for lack of marketability to the quoted market price of the issuer’s unrestricted securities. The valuation for the 250,000 marketable securities categorized as Level 2 was based on the price that MusclePharm paid for these shares in October 2014. The Company categorized its warrants potentially settleable in cash and its options issued to Teva Pharmaceuticals, Inc. as Level 3 fair value measurements. The warrants potentially settleable in cash are measured at fair value on a recurring basis and are being marked to fair value at each reporting date until they are completely settled or meet the requirements to be accounted for as component of stockholders’ equity. The warrants are valued using the Black-Scholes option-pricing model, using assumptions consistent with our application of ASC 718.

     Quoted Prices in Active Markets Significant Other Observable Inputs Unobservable Inputs 
Description June 30, 2014  (Level 1)  (Level 2)  (Level 3) 
Assets:            
Cash and cash equivalents $4,074  $4,074  $-  $- 
Marketable securities  5,719   -   5,719   - 
Total assets $9,793  $4,074  $5,719  $- 
                 
Liabilities:                
Warrants potentially settleable in cash $6,450  $-  $-  $6,450 
Total liabilities $6,450  $-  $-   6,450 
                 
  December 31, 2013  Quoted Prices in Active Markets Significant Other Observable Inputs Unobservable Inputs 
Description   (Level 1)  (Level 2)  (Level 3) 
Assets:                
Cash and cash equivalents $1,034  $1,034  $-  $- 
Total assets $1,034  $1,034  $-   - 
                 
Liabilities:                
Derivative liability $23  $-  $-  $23 
Total liabilities $23  $-  $-   23 

 
F-7

 
Description September 30, 2014  
Quoted Prices in Active Markets
(Level 1)
  
Significant Other Observable Inputs
(Level 2)
  
Unobservable Inputs
(Level 3)
 
Assets:            
Cash and cash equivalents $3,006  $3,006  $-  $- 
Marketable securities  5,543   -   5,543   - 
Total assets $8,549  $3,006  $5,543  $- 
                 
Liabilities:                
Warrants potentially settleable in cash $7,242  $-  $-  $7,242 
Total liabilities $7,242  $-  $-  $7,242 
            
Description December 31, 2013  
Quoted Prices in Active Markets
(Level 1)
  
Significant Other Observable Inputs
(Level 2)
  
Unobservable Inputs
(Level 3)
 
Assets:                
Cash and cash equivalents $1,034  $1,034  $-  $- 
Total assets $1,034  $1,034  $-  $- 
                 
Liabilities:                
Derivative liability $23  $-  $-  $23 
Total liabilities $23  $-  $-  $23 

The company has not transferred any financial instruments into or out of Level 3 classification during the sixnine months ended JuneSeptember 30, 2014. A reconciliation of the beginning and ending Level 3 liabilities for the sixnine months ended JuneSeptember 30, 2014 is as follows:
 
  Fair Value Measurements Using Significant Unobservable Inputs 
  (Level 3) 
Balance, January 1, 2014 $23 
Change in fair value of Teva option  (23)
Estimated fair value of warrants assumed in merger on January 2, 2014  10,475 
Estimated fair value of warrants issued in January common stock sale  3,696 
Change in fair value of warrants for the period ended September 30, 2014  (6,929)
Balance at September 30, 2014 $7,242 
  Fair Value Measurements Using Significant Unobservable Inputs 
  (Level 3) 
Balance, January 1, 2014 $23 
Change in fair value of Teva option  (23)
Estimated fair value of warrants assumed in merger on January 2, 2014  10,475 
Estimated fair value of warrants issued in January common stock sale  3,696 
Change in fair value of warrants for the period ended June 30, 2014  (7,721)
Balance at June 30, 2014 $6,450 
F-8

Note 3 – Stockholders’ equity (deficit)

Preferred Stock — The Company has authorized up to 5,000,000 shares of preferred stock, $0.001 par value per share, for issuance. The preferred stock will have such rights, preferences, privileges and restrictions, including voting rights, dividend rights, conversion rights, redemption privileges and liquidation preferences, as shall be determined by the Company’s board of directors upon its issuance. In connection with the Merger Agreement, the Company issued to Cocrystal Discovery’s security holders 1,000,000 shares of the Company’s Series B Convertible Preferred Stock (“Series B”). The Series B shares: (i) automatically convert into shares of the Company’s common stock at a rate of 205.08308640 shares for each share of Series B at such time that the Company has sufficient authorized capital, (ii) are entitled to vote on all matters submitted to shareholders of the Company and vote on an as converted basis and (iii) have a nominal liquidation preference.

Common Stock — The Company has authorized up to 200,000,000 shares of common stock, $0.001 par value per share, for issuance. As noted above, the shares of Series B will automatically convert into shares of the Company’s common stock at such time that the Company has sufficient authorized capital. In addition to the 205,083,086 shares issuable upon conversion of the Series B, shares of common stock are reserved for future issuance as follows as of JuneSeptember 30, 2014 (in thousands):

  As of JuneSeptember 30, 2014 
Warrants outstanding  26,669 
Stock options outstanding  3,8483,058 
Options reserved for future issuance under the Company's 2007 Incentive Plan  49,27349,454 
Total reserved for future issuance  79,79079,181 

F-8


Note 4 – Warrants

The following is a summary of activity in the number of warrants outstanding to purchase the Company’s common stock for the sixnine months ended JuneSeptember 30, 2014 (in thousands):

 January 2012 warrants  February 2012 warrants  June 2013 warrants  June 2013 warrants  August 2013 warrants  October 2013 warrants  Series A warrants  January 2014 warrants  Total  January 2012 warrants  February 2012 warrants  June 2013 warrants  June 2013 warrants  August 2013 warrants  October 2013 warrants  Series A warrants  January 2014 warrants  Total 
                                                      
Outstanding, January 1, 2014  -   -   -   -   -   -   -   -   -   -   -   -   -   -   -   -   -   - 
Warrants acquired in merger  650   1,000   455   1,864   10,000   200   7,000   -   21,169   650   1,000   455   1,864   10,000   200   7,000   -   21,169 
Warrants issued  -   -   -   -   -   -   -   5,500   5,500   -   -   -   -   -   -   -   5,500   5,500 
Outstanding, June 30, 2014  650   1,000   455   1,864   10,000   200   7,000   5,500   26,669 
Outstanding, September 30, 2014  650   1,000   455   1,864   10,000   200   7,000   5,500   26,669 

Warrants consist of warrants potentially settleable in cash, which are liability-classified warrants, and equity-classified warrants.

Warrants classified as liabilities

Liability-classified warrants consist of warrants issued in connection with equity financings in February 2012, August 2013, October 2013 and January 2014.  These warrants are potentially settleable in cash and were determined not to be indexed to the Company’s own stock and are therefore accounted for as liabilities.

F-9

The estimated fair value of outstanding warrants accounted for as liabilities is determined at each balance sheet date. Any decrease or increase in the estimated fair value of the warrant liability since the most recent balance sheet date is recorded in the consolidated statement of comprehensive income (loss) as other income (expense).changes in fair value of derivative liabilities. The fair value of the warrants classified as liabilities is estimated using the Black-Scholes option-pricing model with the following inputs as of JuneSeptember 30, 2014:

 February 2012 warrants  August 2013 warrants  October 2013 warrants  October 2013 warrants  January 2014 warrants  February 2012 warrants  August 2013 warrants  October 2013 warrants  October 2013 warrants  January 2014 warrants 
                              
Strike price $0.60  $0.40  $0.50  $0.50  $0.50  $0.60  $0.40  $0.50  $0.50  $0.50 
                                        
Expected term (years)  1.6   9.1   4.3   9.3   9.5   1.4   8.9   4.0   9.0   9.3 
Cumulative volatility %  67%  105%  82%  105%  105%  69%  104%  84%  104%  104%
Risk-free rate %  0.35%  2.42%  1.36%  2.44%  2.47%  0.32%  2.42%  1.44%  2.44%  2.47%

The Company’s expected volatility is based on a combination of implied volatilities of similar publicly traded entities given that the Company has limited history of its own observable stock price. The expected life assumption is based on the remaining contractual terms of the warrants. The risk-free rate is based on the zero coupon rates in effect at the balance sheet date. The dividend yield used in the pricing model is zero, because the Company has no present intention to pay cash dividends.
 
Warrants classified as equity

Warrants other than those in the above table were recorded in equity at fair value upon issuance, and are not reported as liabilities on the balance sheet.
 
F-9


Note 5 – Stock-based compensation

As of December 31, 2013, Cocrystal Discovery had 288,000 stock options outstanding.  As a result of the merger between Cocrystal Discovery and Biozone, these options were converted into 4,402,890 stock options in Biozone based on the exchange ratio of 15.28784681 to one.  No additional options were granted in the sixnine months ended JuneSeptember 30, 2014.

The Company recorded approximately $9,000$6,000 and $20,000$25,000 of stock-based compensation related to employee and non-employee stock options for the three months and sixnine months ended JuneSeptember 30, 2014, respectively. As of JuneSeptember 30, 2014, there was $44,000$26,000 of unrecognized compensation cost related to outstanding options that is expected to be recognized as a component of the Company’s operating expenses over a weighted average period of 1.9 years.

As of JuneSeptember 30, 2014, an aggregate of 53,599,046 shares of common stock were reserved for issuance under the Company’s 2007 Incentive Plan, including 3,848,3933,057,564 shares subject to outstanding common stock options granted under the plan and 49,272,85849,454,401 shares available for future grants. The administrator of the plan determines the times when an option may become exercisable.exercisable at the time of grant. Vesting periods of options granted to date have not exceeded four years.  The options generally will expire, unless previously exercised, no later than ten years from the grant date. The company is using unissued shares for all shares issued for options and restricted share awards.

 
  Total number of shares  Weighted Average Exercise Price  Aggregate Intrinsic Value 
Outstanding options at January 1, 2014  4,402,890   0.11  $937,816 
Granted  -   -   - 
Exercised  (477,795)  0.11   (101,293)
Cancelled  (76,702)  0.11   (16,107)
Outstanding at June 30, 2014  3,848,393  $0.11  $808,163 
             
Options exercisable at June 30, 2014  3,918,139  $0.10  $861,991 
F-10

The following schedule presents activity in the Company’s outstanding stock options for the nine months ended September 30, 2014:

  
Total number
of shares
  Weighted Average Exercise Price  Aggregate Intrinsic Value 
Outstanding options at January 1, 2014  4,402,890  $0.11  $1,113,931 
Granted  -   -   - 
Exercised  (1,087,081)  0.11   (273,944)
Cancelled  (258,245)  0.11   (64,561)
Outstanding at September 30, 2014  3,057,564  $0.11  $764,391 
             
Options exercisable at September 30, 2014  2,831,058  $0.10  $736,075 

The aggregate intrinsic value of outstanding and exercisable options at JuneSeptember 30, 2014 was calculated based on the closing price of the Company’s common stock as reported on the Over-the-Counter Bulletin Board and the OTCQx markets on JuneSeptember 30, 2014 of $0.32$0.36 per share less the exercise price of the options. The aggregate intrinsic value is calculated based on the positive difference between the closing fair market value of the company’sCompany’s common stock and the exercise price of the underlying options.
 
Note 6 – Net Income (Loss)Loss per Share
 
The Company accounts for and discloses net income (loss)loss per common share in accordance with FASB ASC Topic 260, “EarningsEarnings Per Share”Share. Basic net income (loss)loss per common share is computed by dividing net income (loss)loss attributable to common stockholders by the weighted average number of common shares outstanding (which includes the common share equivalents of the outstanding Series B preferred shares). Diluted net loss per common share is computed by dividing net loss attributable to common stockholders by the weighted average number of common shares that would have been outstanding during the period assuming the issuance of common shares for all potential dilutive common shares outstanding. Potential common shares consist of shares issuable upon the exercise of stock options and warrants and the conversion of Series A preferred stock in 2013. Because the inclusion of potential common shares would be anti-dilutive for all 2013 and 2014 periods presented diluted net loss per common share is the same as basic net loss per common share for these periods.
 
The following table sets forth the computation of basic and diluted net income (loss)loss per share.
 
  Three Months Ended June 30,  Six Months Ended June 30, 
  2014  2013  2014  2013 
Numerator:            
Net income/(loss) $4,730  $(1,030) $4,357  $(2,088)
Less change in fair value of derivative liability  5,639   -   7,744   - 
Net loss attributable to shareholders  (909)  (1,030)  (3,387)  (2,088)
                 
Denominator:                
Basic and diluted weighted-average shares outstanding  326,760   57,255   326,160   57,255 
                 
Net income (loss) per share:                
Basic $0.01  $(0.02) $0.01  $(0.04)
Diluted $(0.00) $(0.02) $(0.01) $(0.04)
  
Three Months Ended
September 30,
  
Nine Months Ended
September 30,
 
  2014  2013  2014  2013 
             
Numerator:            
Net income/(loss) $(2,549) $(1,005) $1,808  $(3,093)
Less change in fair value of derivative liability  (792  -   6,952   - 
Net loss attributable to shareholders   (1,757)   (1,005)   (5,144)   (3,093)
                 
Denominator:                
Basic and diluted weighted-average shares outstanding  327,209   57,255   326,534   57,255 
                 
Net income (loss) per share:                
Basic $(0.01) $(0.02) $0.01  $(0.05)
Diluted $(0.01) $(0.02) $(0.02) $(0.05)

 
F-10F-11

 
The following table sets forth the number of potential common shares included forexcluded from the 2014 calculations of net income (loss) per diluted share and excluded from the 2013 calculations of net loss per diluted share because their inclusion would be anti-dilutive (in thousands):

  Three and Six months ended June 30, 
  2014  2013 
Options to purchase common stock  3,848   4,403 
Warrants to purchase common stock  26,669   3,969 
Series A convertible preferred stock  -   9,256 
Total  30,517   17,628 

  Three and nine months ended September 30, 
  2014  2013 
Options to purchase common stock  3,058   4,403 
Warrants to purchase common stock  26,669   13,969 
Series A convertible preferred stock  -   9,256 
Total  29,727   27,628 
Note 7 – Marketable securities held
 
On January 2, 2014, Biozone sold substantially all its operating assets to Musclepharm Corporation (“Musclepharm”),MusclePharm, a public company trading on the OTCBB, in exchange for 1,200,000 shares of MusclepharmMusclePharm common stock. 600,000 shares were placed into escrow for a period of 9 months (the “Escrow Period”) to cover indemnification obligations. Additionally, Musclepharm hasMusclePharm had the option to purchase the shares held in escrow at a purchase price of $10.00 per share during the Escrow Period, which ended on October 2, 2014 (the “Call Option”). The remaining 600,000 non-escrowed shares were issued to Biozone upon closing. This transaction occurred immediately prior to the Merger described in Note 1 above. These 600,000 non-escrowed shares were sold for $9.00 per share in June 2014 in a private sale. The unrealized holding gain of $480,000 on these shares was reclassified to realized gain from accumulated other comprehensive income in June 2014.  On September 29, 2014, the Company signed a Memo of Understanding in which it agreed to release 90,000 shares of MusclePharm stock in exchange for a release from all claims which MusclePharm had made concerning assets which it acquired in its purchase of assets from the Company in January 2014. This agreement resulted in recording a net loss of $584,000 in Other income (expense) based on the original basis of the shares received in January 2014 being released for no consideration.  The net loss of $584,000 is presented based on the fair value of these shares of $1,188,000 as of September 30, 2014 offset by the unrealized gain of $604,000 which was reclassified from accumulated other comprehensive income to realized gain as of September 30, 2014.  As of September 30, 2014, therefore, 510,000 shares remained in escrow. MusclePharm did not withdraw the portion of its claim of $3,037,000 that relates to the pending eviction proceedings described in Note 11 below and will continue to hold in escrow 260,000 shares of its stock pending such time as MusclePharm and the Company can reach a mutually agreeable arrangement. In October 2014, MusclePharm exercised its right to repurchase 250,000 shares of MusclePharm shares at $10.00 per share. As of September 30, 2014, these shares are recorded at $2,500,000. As of October 2, 2014, the right of MusclePharm to repurchase additional shares terminated.
 
The estimated fair value of the MusclepharmMusclePharm escrowed securities is determined at each balance sheet date. Any decrease or increase in the estimated fair value of the securities since the most recent balance sheet date is recorded as a component of other comprehensive income (loss). Since the shares held in escrow are subject to restrictions on the Company’s ability to sell and are also subject tothem freely in the Call Option,open market, the fair value of such shares is estimated by applying a discount for lack of marketability and for the Call Option to the quoted market price of unrestricted shares of Musclepharm.MusclePharm. The fair value of the Call Optiondiscount was estimated to be approximately $1,386,000$363,491 as of JuneSeptember 30, 2014 and the discount for lack of marketability was estimated to be approximately $140,000.2014. As a result, the escrowed Musclepharm260,000 MusclePharm shares which will remain in escrow are recorded on the consolidated balance sheet at their estimated fair value of $5,719,000$3,042,509 as of JuneSeptember 30, 2014 which represents a discount totaling $1,526,000 fromand are recorded as long-term assets based on uncertainty regarding when the Company will be able to sell these shares. The market price of $7,245,000those shares was $3,406,000 as of those shares.September 30, 2014. The 250,000 MusclePharm shares which were repurchased by MusclePharm at $10.00 per share in October 2014 are recorded on the consolidated balance sheet at their estimated fair value of $2,500,000.
 
Note 8 – Financing
 
On January 21, 2014, the Company completed the sale of 5,500,000 shares of its common stock in a private placement in exchange for $2,750,000. 5,500,000 warrants to purchase common stock at an exercise price of $0.50 for a period of ten years were issued in conjunction with this sale. These warrants were recorded as liabilities upon issuance due to potential cash settlement provisions, as discussed in Note 4. The fair value of these warrants was estimated to be $3,696,000 at issuance. As this exceeds total proceeds received of $2,750,000, the excess of $946,000 was expensed during the sixnine months ended JuneSeptember 30, 2014.

F-12

Note 9 - Licenses and Collaborations
 
On September 13, 2011, the Company signed a Share Purchase Agreement with Teva Pharmaceuticals Industries Limited (“Teva”). Under the terms of this agreement, Teva purchased at an initial closing 687,442 shares of the Company’s common stock for $7.5 million and, concurrent with the purchase of the common stock, obtained options to purchase up to an additional $37.5 million of the Company’s common stock. Teva has not exercised any options to purchase additional common stock, and all options have expired.

Contemporaneous with the signing of the Share Purchase Agreement, the Company also signed a Research and Collaboration Agreement and an Exclusive License Option Agreement with Teva. Under the terms of the Research and Collaboration Agreement, the Company carried out a research and development program (“R&D Program”) to develop novel therapeutics for Hepatitis C that target the viral polymerase enzyme involved in replication of the virus. The R&D Program has been concluded. Teva's options to extend the R&D Program or to receive a license to the technology developed by the Company under the R&D Program have expired. The Company retains all rights to the technology.
 
F-11


Accounting Treatment
 
The Company determined that Teva’s options to purchase additional shares of common stock were freestanding instruments that were required to be classified as liabilities and carried at fair value under the provisions of ASC 480-10, Distinguishing Liabilities from Equity. Accordingly, the Company allocated the proceeds from the initial $7.5 million investment between the common stock and the options to purchase additional shares of common stock under the terms outlined in the Share Purchase Agreement. The Company recorded a liability of $4.2 million for the initial fair value of Teva’s options in 2011, and allocated the remainder of the proceeds to common stock issued for $3.1 million, net of transaction costs of $172,000.

The liability representing the fair value of the options was included on the accompanying balance sheets as “Derivative liability” and was required to be remeasured at fair value at each reporting date. The fair value of the options to purchase additional common stock was estimated using a probability-weighted Black-Scholes-Merton model. As of JuneSeptember 30, 2014, all such options had expired and the liability was reduced to zero.

Note 10 – Mortgage Notes and Other Receivable

In June 2014, the Company acquired a mortgage note from a bank for $2,626,290 which is collateralized by, among other things, the underlying real estate and related improvements.  The property subject to the mortgage is owned by Daniel Fisher, one of the founders of Biozone, and is currently under lease to MusclePharm.  At JuneSeptember 30, 2014, the carrying amount of the mortgage note receivable was $2,626,290$2,634,019, which consisted of $2,518,433$2,493,264 of principal, $80,218$113,218 of interest and $27,639$27,158 of fees paid to the selling bank.  The mortgage note has a maturity date of August 1, 2032 and bears an interest rate of 7.24%.  The Company records its mortgage note receivable at the amount advanced to the borrower, which includes the stated principal amount and certain loan origination and commitment fees that are recognized over the term of the mortgage note. Interest income is accrued as earned over the term of the mortgage note. The Company evaluates the collectability of both interest and principal of the note to determine whether it is impaired. The note would be considered to be impaired if, based on current information and events, the Company determined that it was probable that it would be unable to collect all amounts due according to the existing contractual terms. If the note were considered to be impaired, the amount of loss would be calculated by comparing the recorded investment to the value determined by discounting the expected future cash flows at the note’s effective interest rate or to the fair value of the Company’s interest in the underlying collateral, less the cost to sell. No impairment loss has been recognized in connection with the mortgage note receivable.
F-13

Note 11- Contingencies
 
From time to time, we are a party to, or otherwise involved in, legal proceedings arising in the normal course of business.  As of the date of this report, except as described below, we are not aware of any proceedings, threatened or pending, against us which, if determined adversely, would have a material effect on our business, results of operations, cash flows or financial position.
 
The Company is named in two legal proceedings both arising out of thatinvolving Daniel Fisher.
The first proceeding is an action filed in Contra Costa County, California  by the landlord, which is an entity managed by Mr. Fisher, to evict MusclePharm as a tenant from real property located at 580 Garcia Avenue, Pittsburg, California (the “Garcia Property”our now inactive subsidiary, Biozone Laboratories, Inc. (“Biozone Labs”) previously leased. MusclePharm purchased our operating assets from us on January 2, 2014, and we immediately merged with Cocrystal Discovery, Inc. (“Cocrystal Discovery”).  Prior to our sale of our operating assets to MusclePharm, we gave notice of the locationassignment of the lease to MusclePharm and requested that the founder/landlord approve the assignment.  The lease requires landlord approval, said approval not to be unreasonably denied.  The landlord failed to respond to our request, but gave notice to the lender that held a mortgage note on the property of the asset sale and assignment of the lease to MusclePharm. Prior notice and consent of a lease assignment or change of control was also required under the terms of the loan documents related to the property, although no notice was given when we acquired Biozone Labs in 2011.
On March 27, 2014, the landlord filed suit in the Contra Costa County Court against us and Biozone Labs, as well as MusclePharm, alleging the assignment of the lease to MusclePharm was a violation of the lease and its provision requiring the landlord’s consent for a change of control.  As indicated above, the landlord failed to either approve or reject the proposed assignment when requested in December 2013.  Further, the landlord has continued to cash the rent checks from whichMusclePharm (from January 2014 through November 2014), without objection or reservation of its rights. Only upon the lender’s default and acceleration of the note did the landlord express any objection to the assignment.  The Company’s position in the litigation will include that by engaging in the foregoing conduct, the landlord waived its right to assert a default due to the change in control.  
We agreed to indemnify MusclePharm for its expenses if it were evicted as the result of any action taken by the landlord. The costs of any move would be substantial.   As described in Note 7, MusclePharm has made a claim in the amount of $3,037,000 and the Company previously conducted its principal operations.  With respecthas agreed to a Memo of Understanding in which it is agreed that the claim concerningCompany will continue to escrow 260,000 shares of MusclePharm stock shares pending such time as MusclePharm and the loan securedCompany can reach a mutually agreeable arrangement.  There have been no material recent developments, and the proceeding is not presently being actively litigated. We intend to vigorously defend the action to prevent MusclePharm’s eviction.
In the second proceeding, the Company has been named as a party to a lawsuit filed on April 15, 2014 in Contra Costa County, California by the Garcia Property – said loan being guaranteedsame entity managed by oneMr. Fisher. Also named in this action are two of the Company’s subsidiaries BioZone Laboratories –Labs and Cocrystal Discovery.   The action seeks recovery on a promissory note purportedly executed by BioZone Labs in the loan, asprincipal amount of $295,000 in 2007, well before our January 2, 2014 merger with Cocrystal Discovery.   Motions challenging the sufficiency of the allegations in the Complaint were filed in the third quarter, 2014, the motions were granted and plaintiff was given an opportunity to amend the complaint, and plaintiff has filed an amended complaint. The Company intends to vigorously defend the action.
Previously the lender to the Fisher entity which owns the Contra Costa County property had threatened to foreclose, based upon, among other things, the change of control. Mr. Fisher was one of the founders of Biozone Labs and financed the purchase of the property from which Biozone Labs’ principal operations were then conducted.  Biozone Labs was required to guarantee the note and performance under the deed of trust securing repayment of the note (together with the founder, his wife and the other founder). As indicated in Note 10 to the Consolidated Financial Statements, the note and deed of trust was purchased by the Company.

The first proceeding disclosedCompany in June 2014. This removed the immediately preceding Form 10-Q –threat of a lawsuit against Biozone Labs and us for the action by the founder/landlord in Contra Costa County is still pending and its status is unchanged.  However, the Company’s purchaseprincipal of the loan secured by the Garcia Property potentially affords the Companynote and its subsidiaries additional defenses to the claims of the founder/landlord in that action.related charges including legal fees.
 

Finally, the Company has been named as a party to a new lawsuit filed on April 15, 2014 in Contra Costa County by the same founder and former officer of BioZone Laboratories.  Also named in this new action are two of the Company’s subsidiaries – BioZone Laboratories and Cocrystal Discovery.  Filed in the name of the entity controlled by the founder/former officer which currently holds title to the Garcia Property, the action seeks recovery on a promissory note purportedly delivered by BioZone Laboratories in the amount of $295,000.   A motion challenging the sufficiency of the allegations in the Complaint was filed. The Company intends to vigorously defend the action.

ITEM 2.. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

Forward-Looking Statements
 
Except for the historical information contained herein or incorporated by reference, this Annual Report and the information incorporated by reference contains forward-looking statements that involve risks and uncertainties. These statements include projections about our accounting and finances, plans and objectives for the future, future operating and economic performance and other statements regarding future performance. These statements are not guarantees of future performance or events. Our actual results may differ materially from those discussed here. Factors that could cause or contribute to differences in our actual results include those discussed in the following section, and those discussed in Part II, entitled “Management’s Discussion and Analysis of Financial Condition and Results of Operations”.
  
Overview-
 
Cocrystal Pharma, Inc. ("Cocrystal") is a biotechnology company which develops novel medicines for use in the treatment of human viral diseases. Cocrystal has been developing novel technologies and approaches to create first-in-class and best-in-class antiviral drug candidates since its initial funding in 2008. Subsequent funding was provided to Cocrystal Discovery by Teva Pharmaceuticals Industries, Ltd. in 2011. Our focus is to pursue the development and commercialization of broad-spectrum antiviral drug candidates that will transform the treatment and prophylaxis of viral diseases in humans. By concentrating our research and development efforts on viral replication inhibitors, we plan to leverage our infrastructure and expertise in these areas.

Highlights

During the three months ended Juneending on September 30, 2014, the Company, through Cocrystal Discovery, focused on its research and development efforts as it moves toward seeking regulatory approval to commence clinical trials. We expect to file with appropriate regulators as follows:
 
 
Hepatitis C.C. We have selected a lead molecule to advance for IND-enabling studies.studies, and initiated non-GLP and GLP manufacturing of the lead molecule.  Cocrystal’s non-nucleoside lead is highly potent, effective against all HCV genotypes, and shows a favorable pharmacokinetic profile.  We expect to file regulatory submissions to initiate clinical trials in earlythe first half of 2015.   We are also pursuing inhibitors of the HCV NS3 helicase.  Cocrystal’s helicase inhibitor will be a first-in-class drug, and may be combined with an RNA polymerase inhibitor for greater effectiveness and a higher barrier to resistance.

 
Influenza.  We have developed novel inhibitors of the influenza endonuclease enzyme that is essential for viral genome replication.  We expect to file an Investigational New Drug application with the U.S. Food & Drug Administration in December 2015;2015.

On March 18, 2014, we reincorporated in Delaware under the name Cocrystal Pharma, Inc. ("Cocrystal"). We were previously incorporated in Nevada under the name Biozone Pharmaceuticals, Inc ("Biozone"). Our only operating subsidiary is Cocrystal Discovery, Inc., which we merged with on January 2, 2014.  Immediately prior to the Cocrystal Discovery merger, on January 2, 2014, we completed the sale of substantially all of our operating assets to a subsidiary of MusclePharm Corporation ("MusclePharm") in exchange for common stock of MusclePharm. For a description of the assets we retained immediately upon completion of the MusclePharm asset sale, see Note 7. This transaction was accounted for as a reverse merger between Biozone and Cocrystal Discovery.
Dengue Fever, Norovirus, and Rhinovirus.  We have identified novel inhibitors of Dengue virus, Norovirus, and rhinovirus polymerases.  We plan to develop broad-spectrum lead molecules which are inhibitors of the polymerase enzyme.
 
Ebola.We have recently developed a novel high throughput screening technology for inhibitors of an essential Ebola virus gene product. Using the screening assay, we plan to develop lead molecules for treating Ebola infections which we can license to pharmaceutical or biotechnology companies.


Results of Operations for the Three Months and SixNine Months Ended JuneSeptember 30, 2014 and JuneSeptember 30, 2013

The following discussion consists of the results of operations of Cocrystal Discovery combined with ongoing corporate overhead at the Cocrystal or public company level.

As stated above, we are focused on research and development of novel medicines for use in the treatment of human viral diseases. Accordingly, we had no revenue for the three months and sixnine months ended JuneSeptember 30, 2014 and 2013.  For the three months ended JuneSeptember 30, 2014, we had a net loss of approximately $2,549,000 compared to a net loss of approximately $1,005,000 for the same period in 2013. For the nine months ended September 30, 2014, we had net income of approximately $4,730,000$1,808,000 compared to a net loss of approximately $1,030,000 for the same period in 2013. For the six months ended June 30, 2014, we had net income of approximately $4,357,000 compared to a net loss of approximately $2,088,000$3,093,000 for the same period in 2013. We reported net income for the three months and sixnine months ended JuneSeptember 30, 2014 primarily due to the substantial decrease in the fair value of our outstanding warrants, which are accounted for as liabilities.  Under accounting principles generally accepted in the United States, we record other income or expense for the change in fair value of our outstanding warrants that are accounted for as liabilities during each reportreporting period. If the value of the warrants decreases during a period, which occurred during the three and sixnine months ended JuneSeptember 30, 2014, we record other income.  If the fair value of the warrants were to increase during the period, which it did in the three months ended September 30, 2014, we would record other expense.  The fair value of our outstanding warrants is inversely related to the fair value of the underlying common stock; as such, a decrease in the fair value of our common stock during a given period generally results in other income while an increase in the fair value of our common stock generally results in other expense.  This other income or expense is non cash.  We believe investors should focus on our cash flows contained in our unaudited Consolidated Financial Statements and operating loss rather than net income or loss for the periods presented. Other income or (loss) related to the change in fair value of our liability-classified warrants for the three and sixnine months ended JuneSeptember 30, 2014 was $5,639,000($792,000) and $7,744,000,$6,952,000, respectively, and our operating loss for the three months and sixnine months ended JuneSeptember 30, 2014 was $1,387,000$1,219,000 and $2,919,000,$4,139,000, respectively, compared to $1,031,000$1,005,000 and $2,090,000$3,095,000 for the same periods in 2013.

Research and Development Expense

Research and development expense consists primarily of compensation-related costs for our 138 employees dedicated to research and development activities and for our Scientific Advisory Board members, as well as lab supplies, lab services, and facilities and equipment costs. We expect research and development expenses to increase in future periods as we expand our pre-clinical development activities.

Total research and development expenses were approximately $888,000$866,000 for the three months ended JuneSeptember 30, 2014, compared with $980,000$950,000 for the three months ended JuneSeptember 30, 2013. The decrease of $92,000,$84,000, or 9%, was due to a $50,000$28,000 decrease in the personnel costs, a $30,000$36,000 decrease in lab supply and services costs and a $12,000$20,000 decrease in other operatinglegal costs.

Total research and development expenses were approximately $1,853,000$2,722,000 for the sixnine months ended JuneSeptember 30, 2014, compared with $1,986,000$2,936,000 for the sixnine months ended JuneSeptember 30, 2013. The decrease of $133,000,$214,000, or 7%, was due to a $75,000$110,000 decrease in the personnel costs, a $30,000$70,000 decrease in lab supply and services costs, and facilities costs and a $28,000$34,000 decrease in other operating costs.
 
The company did not renew its lease on the Mountain View, California lab facility and has consolidated all operations into its Bothell, Washington headquarters, which will result in a non-material reduction in expenses. 

General and Administrative Expense

General and administrative expense includes compensation-related costs for our employees dedicated to general and administrative activities, legal fees, audit and tax fees, consultants and professional services, and general corporate expenses.

General and administrative expense was $499,000expenses were approximately $353,000 for the three months ended JuneSeptember 30, 2014, compared with $51,000$55,000 for the three months ended JuneSeptember 30, 2013. The increase of $448,000,$298,000, or 878%542%, was due to a $116,000$102,000 increase in compensation-related costs, a $280,000$108,000 increase in accounting, legal and other professional services associated with the merger and financing costs and our status as a public company, and an $88,000 increase in facilities costs due to the additional lease in Princeton, New Jersey.

General and administrative expense was $1,417,000 for the nine months ended September 30, 2014, compared with $159,000 for the nine months ended September 30, 2013. The increase of $1,258,000, or 791%, was due to a $318,000 increase in compensation-related costs, a $761,000 increase in accounting, legal and other professional services associated with the merger and financing costs, and a $52,000$179,000 increase in facilities and other operating costs.

  Future General and administrative expense was $1,066,000 forAdministrative expenses are expected to continue at the six months ended June 30, 2014, compared with $104,000 forcurrent levels other than specific costs related to the six months ended June 30, 2013. The increase of $962,000, or 924%, was due to a $220,000 increase in compensation-related costs, a $660,000 increase in accounting, legal and other professional services associated with the merger and financing costs, and a $82,000 increase in facilities costs.merger.
 

Interest Income/Expense

Interest income (expense)was $50,000 for the three months and nine months ended September 30, 2014, which represents interest earned on the mortgage note we acquired in June 2014.  Interest expense was negligible for each of the three months and sixnine months ended JuneSeptember 30, 2014 and 2013. The key objectives of our investment policy are to preserve principal and ensure sufficient liquidity, so our invested cash may not earn as high a level of income as longer-term or higher risk securities, which generally have less liquidity and more volatility. We expect interest income to increase subsequent to June 30, 2014 as a result of the mortgage note we acquired in June 2014.

Other Income/Expense

Other incomeexpense was $6,117,000 and $7,276,000$1,330,000 for the three months ended September 30, 2014 and sixOther income was $5,947,000 for the nine months ended JuneSeptember 30, 2014, compared with $1,000$0 and $2,000 for the three months and sixnine months ended JuneSeptember 30, 2013.

The increase in the other incomeexpense of $6,116,000 and $7,274,000$1,330,000 in the three months and six months ended JuneSeptember 30, 2014 was all non-cash and was due to an increase in the $792,000 fair value of derivative liabilities as our stock price increased and due to the $584,000 loss on the return of escrowed shares.  The increase of Other income of $5,945,000 in the nine months ended September 30, 2014 was all non-cash and was due to a $ 6,952,000 decrease in the fair value of derivative liabilities as our stock price decreased, offset by expense of $946,000 for the difference between the proceeds received in our January 2014 common stock financing and the fair value of the warrants issued with the common stock.stock and the loss on return of escrowed shares of $584,000.  These derivative liabilities are warrants to acquire the Company’s common stock that are potentially settleable in cash.

Liquidity and Capital Resources

We had cash and cash equivalents and marketable securities of approximately $9.8$3.0 million as of JuneSeptember 30, 2014, compared with $1.0 million as of December 31, 2013. The increase of $8.8$2.0 million in our cash and cash equivalents from December 31, 2013 to JuneSeptember 30, 2014 was attributable primarily to our $2.75 million common stock financing which closed in January 2014, as well as the cash acquired in the reverse merger and the proceeds from sales of certain of the marketable securities acquired in the reverse merger, offset by our operating loss for the period.  In addition to the $3.0 million of cash and cash equivalents, we also held MusclePharm common stock with a fair value of $5.5 million as of September 30, 2014, of which $2.5 million was sold subsequent to September 30, 2014, with the remaining $3.0 million of marketable securities held in escrow pending resolution of the matters discussed further below.

For the sixnine months ended JuneSeptember 30, 2014, net cash used in operating activities was $3,118,000$4,257,000, compared to net cash used in operating activities of $1,930,000$2,878,000 for the same period in 2013. In 2014, net cash used in operating activities was primarily due to the net operating loss of $2,919,000$4,139,000 and cash used to pay down current liabilities of $312,000,$358,000, much of which related to accounts payable acquired in the reverse merger.  For the sixnine months ended JuneSeptember 30, 2014, net cash provided by investmentinvesting activities was $3,351,000$3,348,000 compared to no cash generated for the same period in 2013.  In 2014, net cash generated by investmentinvesting activities was primarily due to the sale of marketable securities for $5,400,000, $589,000 of cash acquired in the acquisition of Biozone Laboratories, Inc. and the investment in a mortgage note receivable of $2,626,000.  For the sixnine months ended JuneSeptember 30, 2014, net cash provided by financing activities was $2,807,000$2,865,000, compared to cash generated of $5,000 for the same period in 2013.  In 2014, net cash generated by financing activities was primarily due to the proceeds from the issuance of common stock and warrants of $2,750,000.
 
Cocrystal has $3,544,000We have $5,292,000 in cash and cash equivalents as of August 7, 2014;November 6, 2014 which includes the $2,500,000 received from MusclePharm; in addition it owns 600,000we own 260,000 shares of MusclePharm, Inc. common stock which had a fair market value of $6,600,000$3,043,000 at August 7,September 30, 2014. The 600,000 shares are heldMusclePharm, Inc. will continue to hold in escrow until October 2014these shares pending such time as MusclePharm and we can reach a mutually agreeable arrangement of MusclePharm’s claim that relates to satisfy any breaches of representations under the Asset Purchase Agreement.   Assuming thatcontingency described in Note 11 to the consolidated financial statements.  As we are able to sell the shares of MusclePharm at current market prices , we  have sufficient cash to fund our current operating plan for at least the next 12 months.  Otherwise we will have to raise capital through the sale of equity and/or debt securities.  As Cocrystal continuescontinue to incur losses, achieving profitability is dependent upon the successful development, approval and commercialization of itsour product candidates, which is a number of years in the future. Once that occurs, we will have to achieve a level of revenues adequate to support Cocrystal’sour cost structure. CocrystalWe may never achieve profitability, and unless and until it does, Cocrystalwe do, we will continue to need to raise additional capital. Over the next 12 months ending JuneSeptember 30, 2015, we estimate negative cash flow of approximately $6.0 million.  Management intends to fund future operations through additional private or public debt or equity offerings, and may seek additional capital through arrangements with strategic partners or from other sources. In addition we may, if appropriate or necessary, sell the MusclePharm common stock onceat such time as they are released from escrow.escrow, which is dependent on resolution of the contingency described in Note 11 to the financial statements. There can be no assurances, however, that additional funding will be available on terms acceptable to Cocrystal,us, or at all.
 

Cautionary Note Regarding Forward-Looking Statements

This report includes forward-looking statements including statements regarding our anticipated regulatory filings, cash flow deficit and liquidity.   The words “believe,” “may,” “estimate,” “continue,” “anticipate,” “intend,” “should,” “plan,” “could,” “target,” “potential,” “is likely,” “will,” “expect” and similar expressions, as they relate to us, are intended to identify forward-looking statements.  We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our financial condition, results of operations, business strategy and financial needs.  
 
The results anticipated by any or all of these forward-looking statements might not occur. Important factors that could cause actual results to differ from those in the forward-looking statements include our ability to raise sufficient capital, unanticipated events which adversely affect the timing and success of our regulatory filings, failure to develop products which are deemed safe and effective and other issues which affect our ability to commercialize our product candidates.  Further information on our risk factors is contained in our filings with the SEC, including our Annual Report on Form 10-K, as amended. We undertake no obligation to publicly update or revise any forward-looking statements, whether as the result of new information, future events or otherwise.
 
Recent Accounting Pronouncements

In June 2014, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) No. 2014-10, Development Stage Entities: Elimination of Certain Financial Reporting Requirements, Including an Amendment to Variable Interest Entities Guidance in Topic 810, Consolidation, which eliminates the concept of a development stage entity, or DSE, in its entirety from GAAP.  Under previous guidance, DSEs were required to report incremental information, including inception-to-date financial information, in their financial statements.  A DSE is an entity devoting substantially all of its efforts to establishing a new business and for which either planned principal operations have not yet commenced or have commenced but there has been no significant revenues generated from that business.  Entities classified as DSEs are no longer subject to these incremental reporting requirements after adopting ASU No. 2014-10.  ASU No. 2014-10 is effective for fiscal years beginning after December 15, 2014, with early adoption permitted.  Prior to the issuance of ASU No. 2014-10, we had met the definition of a DSE since its inception.  We elected to adopt this ASU early, and therefore we have eliminated the incremental disclosures previously required of DSEs, starting withDSEs.

In August 2014, the FASB issued ASU No. 2014-15, Disclosure of Uncertainties about an Entity’s Ability to Continue as a Going Concern (ASU 2014-15). ASU 2014-15 requires management to determine whether substantial doubt exists regarding the entity’s going concern presumption, which generally refers to an entity’s ability to meet its obligations as they become due. If substantial doubt exists but is not alleviated by management’s plan, the footnotes must specifically state that “there is substantial doubt about the entity’s ability to continue as a going concern within one year after the financial statements are issued”.  In addition, if substantial doubt exists, regardless of whether such doubt was alleviated, entities must disclose (a) principal conditions or events that raise substantial doubt about the entity’s ability to continue as a going concern (before consideration of management’s plans, if any); (b) management’s evaluation of the significance of those conditions or events in relation to the entity’s ability to meet its obligations; and (c) management’s plans that are intended to mitigate the conditions or events that raise substantial doubt, or that did alleviate substantial doubt, about the entity’s ability to continue as a going concern.  If substantial doubt has not been alleviated, these disclosures should become more extensive in subsequent reporting periods as additional information becomes available.  In the period that substantial doubt no longer exists (before or after considering management’s plans), management should disclose how the principal conditions and events that originally gave rise to substantial doubt have been resolved.  The ASU applies prospectively to all entities for annual periods ending after December 15, 2016, and to annual and interim periods thereafter.  Early adoption is permitted. We have not adopted the provisions of this Quarterly Report on Form 10-Q.ASU.

Critical Accounting Policies and Estimates

In our Annual Report on Form 10-K/A for the year ended December 31, 2013 and in the 8-K/A filed on March 20, 2014 with the financial statements of Cocrystal Discovery, Inc. for the year ended December 31, 2013, we disclosed our critical accounting policies and estimates upon which our financial statements are derived. There have been no changes to these policies since December 31, 2013. Readers are encouraged to review these disclosures in conjunction with the review of this report.
 
ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.
Not applicable to smaller reporting companies.

ITEMITEM 3 4.. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.
Not applicable to smaller reporting companies.
ITEM 4. CONTROLS AND PROCEDURES

Evaluation of Disclosure Controls and Procedures
 
The Company maintains a set of disclosure controls and procedures designed to ensure that information required to be disclosed by the Company in reports that it files or submits under the Securities Exchange Act of 1934 is recorded, processed, summarized, and reported within the time periods specified in Securities and Exchange Commission’s rules and forms.  Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed by the Company in the reports that it files or submits under the Securities Exchange Act of 1934 is accumulated and communicated to the Company’s management, including its principal executive and principal financial officers, as appropriate, to allow timely decisions regarding required disclosure.  An evaluation was carried out under the supervision and with the participation of the Company’s management, including the Chief Executive Officer and Chief Financial Officer, of the effectiveness of the our disclosure controls and procedures.  Based on that evaluation, the Chief Executive Officer and Chief Financial Officer have concluded that as of JuneSeptember 30, 2014, our disclosure controls and procedures were not effective, due to the material weakness in our internal control over financial reporting as described below, to ensure that information required to be disclosed was accumulated and communicated to management as appropriate to allow timely decisions regarding required disclosure.
  
Material Weakness
 
A material weakness is a deficiency, or a combination of deficiencies, in internal control over financial reporting, such that there is a reasonable possibility that a material misstatement of the Company’s annual or interim financial statements will not be prevented or detected on a timely basis. Based on our assessment using the criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (“COSO”) in Internal Control-Integrated Framework (1992), management concluded that we did not maintain effective internal control over financial reporting as of December 31, 2013, because of a material weakness relating to accounting for complex financial instruments. Specifically, we did not maintain effective controls over the identification and proper accounting treatment of certain terms and conditions in agreements that contained complex financial instruments, including derivatives. This material weakness resulted in a misstatement of our liabilities and non-cash expense relating to the changes in fair value of the derivative instruments, which was identified by our independent auditors in connection with their audit of Cocrystal Discovery’s financial statements as of and for the year ended December 31, 2013.  This material weakness still exists as of JuneSeptember 30, 2014.  This deficiency could result in misstatements of the aforementioned accounts and disclosures that could result in a material misstatement of the consolidated financial statements that would not be prevented or detected.

Remediation Plan
 
Management has been actively engaged in developing a remediation plan to address the material weakness. Implementation of the remediation plan is in process and consists of establishing a formal review process of non-routine and complex transactions, including but not limited to equity transactions and licensing transactions, and to utilize outside consultants as necessary in evaluating the accounting for transactions containing complex financial instruments or derivatives. As of June 30,November 14, 2014, management has not yet completed these remediation efforts.
 
Management believes the foregoing efforts will effectively remediate the material weakness. As the Company continues to evaluate and work to improve its internal control over financial reporting, management may execute additional measures to address potential control deficiencies or modify the remediation plan described above. Management will continue to review and make necessary changes to the overall design of the Company’s internal control.


PARTPART II — OTHER INFORMATION
 
ITEMITEM 1. LEGAL PROCEEDINGS-PROCEEDINGS

From time to time, we are a party to, or otherwise involved in, legal proceedings arising in the normal course of business.  As of the date of this report, except as described below, we are not aware of any proceedings, threatened or pending, against us which, if determined adversely, would have a material effect on our business, results of operations, cash flows or financial position.
 
As disclosed in the Company’s Form 10-Q for the quarterly period ended March 31, 2014, the Company faced one actual and one potential legal proceeding both arising out of that real property located at 580 Garcia Avenue, Pittsburg, California (the “Garcia Property”) – the location from which the Company previously conducted its principal operations.  With respect to the potential claim concerning the loan secured by the Garcia Property – said loan being guaranteed by one of the Company’s subsidiaries, BioZone Laboratories – the loan, as indicated in Note 10 to the Consolidated Financial Statements, was purchased by the Company.  How this will affect the existing default and foreclosure proceedings is uncertain, as the loan now appears to be in monetary default as a result of the non-payment of principal and interest to the Company by the owner of the Garcia Property – an entity controlled by the founder and former President of BioZone Laboratories.

The second proceeding is the action by the founder/landlord in Contra Costa County is still pending and its status is unchanged.  However, the Company’s purchase of the loan secured by the Garcia Property potentially affords the Company and its subsidiaries additional defenses to the claims of the founder/landlord in that action.

Finally, the Company has been named asWe are a party to a newtwo lawsuits which have previously been reported. There were no material developments in either lawsuit filed on April 15,during the quarter ended September 30, 2014. Subsequent to the quarter ended September 30, 2014, in Contra Costa County by the same founder and former officer of BioZone Laboratories.  Also named in this new action are two of the Company’s subsidiaries – BioZone Laboratories and Cocrystal Discovery.  FiledCourt in the name of the entity controlled by the founder/former officer which currently holds titlelawsuit seeking to the Garcia Property, the action seeks recoveryrecover on a promissory2007 $295,000 note purportedly delivered by BioZone Laboratoriesdue in the amount of $295,000.  To date, neither the Company nor BioZone Laboratories have been served with the Complaint.  Cocrystal Discovery has filed a motion challenging the paucity of factual allegations inNovember 2008, dismissed the Complaint since it was acquired by the Companywith leave to amend. The Plaintiff subsequently filed an amendment on January 2,November 10, 2014. Cocrystal Discovery was not a maker or guarantor of the note which was signed a number of years before the January 2, 2014 merger. There is no legal basis for the suit against it.  Once served, the Company intends to vigorously defend the action.

ITEMITEM 1.A RISK FACTORS

Not applicable to smaller reporting companies.

ITEM
ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

None.

ITEMITEM 3. DEFAULTS UPON SENIOR SECURITIES

None

ITEMITEM 4. MINE SAFETY DISCLOSURES

Not Applicable

ITEMITEM 5. OTHER

None
 
ITEMITEM 6. EXHIBITS

The exhibits listed in the accompanying “Index to Exhibits” are filed or incorporated by reference as part of this Form 10-Q.


SIGNATSIGNATURESURES

Pursuant to the requirements 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.


 Cocrystal Pharma, Inc.
  
Dated: AugustNovember 14, 2014By:  
/s/ Gary Wilcox
Gary Wilcox
 
Gary Wilcox
Chief Executive Officer
(Principal Executive Officer)
 
Dated: AugustNovember 14, 2014By:  
/s/ Gerald McGuire
Gerald McGuire
 
Gerald McGuire
Chief Financial Officer
(Principal Financial Officer)




EXHIBIT
EXHIBIT INDEX
 
Exhibit No.
 Exhibit Description Incorporated by Reference 
Filed or
Furnished Herewith
  Form Date Number 
           
10.1Memorandum of UnderstandingFiled
31.1
 
Certification of Principal Executive Officer (302)
       
Filed
31.2
 
Certification of Principal Financial Officer (302)
       
Filed
32.1
 
Certification of Principal Executive and Principal Financial Officer (906)
       
Furnished**
101.INS
 
XBRL Instance Document
       
Filed
101.SCH
 
XBRL Taxonomy Extension Schema Document
       
Filed
101.CAL
 
XBRL Taxonomy Extension Calculation Linkbase Document
       
Filed
101.DEF
 
XBRL Taxonomy Extension Definition Linkbase Document
       
Filed
101.LAB
 
XBRL Taxonomy Extension Label Linkbase Document
       
Filed
101.PRE
 
XBRL Taxonomy Extension Presentation Linkbase Document
       
Filed
 
** This exhibit is being furnished rather than filed and shall not be deemed incorporated by reference into any filing, in accordance with Item 601 of Regulation S-K.
 
Copies of this report (including the financial statements) and any of the exhibits referred to above will be furnished at no cost to our shareholders who make a written request to our Corporate Secretary at Cocrystal Pharma, Inc., 19805 North Creek Parkway, Bothell, Washington, 98011.


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