OREANDA-NEWS. August 10, 2016. Fortress Biotech, Inc. (NASDAQ:FBIO) (Fortress), a biopharmaceutical company dedicated to acquiring, developing and commercializing novel pharmaceutical and biotechnology products, today announced its financial results and recent corporate highlights for the quarter ended June 30, 2016.

Dr. Lindsay A. Rosenwald, Chairman, President and CEO of Fortress, said, During the second quarter of 2016, we attained several milestones, including the commercialization of our first two products from Journey Medical Corporations (Journey) dermatology franchise: Luxamend Wound Cream and Ceracade Skin Barrier Emulsion.

Our subsidiary Checkpoint Therapeutics, Inc. (Checkpoint Therapeutics) also acquired an exclusive, worldwide license to BRD4-inhibiting (from the Bromodomain and Extra-Terminal motif (BET) inhibitor class of anti-cancer proteins) compounds for solid tumors from Jubilant Biosys Limited (Jubilant).  In addition, Checkpoint Therapeutics entered a sublicense agreement with TG Therapeutics, Inc., a related party (TG Therapeutics), to develop and commercialize the BRD4-inhibiting compounds for hematological malignancies, while Checkpoint Therapeutics retains the right to develop and commercialize these compounds for solid tumors. We believe clinical and corporate developments such as these will help position us to diversify our pipeline during the second half of 2016.

Financial Results:

  • At June 30, 2016, Fortress consolidated cash and cash equivalents totaled \\$71.3 million compared to \\$81.4 million at March 31, 2016 and \\$98.2 million as of December 31, 2015, a decrease of \\$10.1 million for the quarter, of which \\$6.6 million relates to our subsidiaries, and \\$26.9 million year-to-date, of which \\$16.1 million relates to our subsidiaries. These totals exclude restricted cash of \\$14.6 million.
  • Total revenue for the second quarter of 2016 was \\$2.2 million consisting of \\$1.0 million of net product revenue from our subsidiary Journey and \\$1.2 million of collaboration revenue from a related party, compared with no revenue reported during last years second quarter. \\$2.9 million in total revenue was reported for the first six months of 2016 consisting of \\$1.4 million of net product sales from Journey and \\$1.5 million of collaboration revenue from a related party, compared with \\$0.5 million of collaboration revenue from a related party reported for the first six months of 2015. 
  • Research and development expenses were \\$6.3 million, of which \\$4.0 million relates to our subsidiaries for the second quarter of 2016 and \\$14.1 million, of which \\$9.0 million relates to our subsidiaries for the first six months of 2016. This compares with \\$2.4 million, of which \\$1.1 million relates to our subsidiaries for the second quarter of 2015 and \\$4.1 million, of which \\$1.2 million relates to our subsidiaries for the first six months of 2015. Noncash stock-based compensation expense included in research and development for the second quarter of 2016 was \\$1.1 million, compared to \\$0.6 million for the second quarter of 2015, and \\$2.4 million for the first six months of 2016, compared with \\$0.9 million for the first six months of 2015.
  • Research and development licenses acquired expenses were \\$2.0 million for the second quarter of 2016 and \\$2.1 million for the first six months of 2016, compared to \\$1.5 million for the second quarter 2015 and  \\$9.0 million for the first six months of 2015.
  • General and administrative expenses were \\$8.6 million, of which \\$3.7 million relates to our subsidiaries for the second quarter of 2016 and \\$16.6 million, of which \\$6.6 million relates to our subsidiaries for the first six months of 2016, compared to \\$3.8 million, of which \\$0.3 million relates to our subsidiaries for the second quarter of 2015 and \\$7.3 million, of which \\$1.6 million relates to our subsidiaries for the first six months of 2015. Noncash stock-based compensation expense included in general and administrative for the second quarter of 2016 was \\$1.9 million, compared to \\$1.3 million for the second quarter of 2015, and \\$3.5 million for the first six months of 2016, compared with \\$2.5 million for the first six months of 2015.
  • Net loss was \\$12.5 million, or \\$0.31 per share, for the second quarter of 2016, compared to a net loss of \\$6.2 million, or \\$0.16 per share, for the second quarter of 2015.  For the first six months of 2016, net loss was \\$24.7 million or \\$0.62 per share, compared with \\$18.2 million or \\$0.47 per share in the first six months of 2015.

Recent Corporate Highlights:

Avenue Therapeutics

  • Avenue completed an End-of-Phase 2 (EOP2) meeting with the FDA and, based on the outcome of the EOP2 meeting, Avenue anticipates that its Phase 3 program will consist of three studies: an efficacy and safety study in an orthopedic model, an efficacy and safety study in a soft tissue model, and an open label safety study.

Checkpoint Therapeutics

  • In May 2016, Jubilant and Checkpoint Therapeutics announced the signing of an exclusive, worldwide license agreement under which Jubilant out-licensed to Checkpoint Therapeutics a family of patents covering compounds that inhibit BRD4, a member of the BET domain for cancer treatment. In connection with the license agreement with Jubilant, Checkpoint Therapeutics entered into a sublicense agreement with TG Therapeutics to develop and commercialize the licensed compounds for hematological malignancies, while Checkpoint Therapeutics retains the right to develop and commercialize these compounds for solid tumors.

Journey Medical Corporation

  • In June 2016, sales began for Luxamend Wound Cream and Ceracade Skin Barrier Emulsion, the first two products in Journeys dermatology franchise. Both products were showcased at the 2016 American Academy of Dermatology (AAD) Summer Meeting in July 2016.
  • In July 2016, Journey received FDA approval for the manufacturing of a product for the treatment of acne, for which it had entered into a license and supply agreement in 2015. Journey expects sales of this product to begin in the fourth quarter of 2016.

Mustang Bio, Inc.

  • In April 2016, Mustang announced that two abstracts pertaining to MB-101 (IL13R?2?specific CAR-T cells) for the treatment of glioblastoma were selected for presentation at the American Society of Gene and Cell Therapys 19th Annual Meeting (ASGCT). Pre-clinical and preliminary Phase I data were presented at ASGCT.
  • In May 2016, an oral presentation related to MB-101 (IL13R?2?specific CAR-T cells) was presented by City of Hope investigators at the ASGCT at the Marriott Wardman Park Hotel in Washington, DC.

 Fortress Biotech

  • On June 10, 2016, CB Pharma Acquisition Corp (CB Pharma) held an extraordinary general meeting of its shareholders. At such meeting, the shareholders approved each of the following items: (i) an amendment to the CB Pharmas Amended and Restated Memorandum and Articles of Association (the Charter) to extend the date by which CB Pharma has to consummate a business combination from June 12, 2016 to December 12, 2016 (the Extension), (ii) an amendment to the Charter to allow the holders of the CB Pharmas ordinary shares issued in the initial public offering to elect to convert their shares into their pro rata portion of the funds held in trust, if the Extension is approved, and (iii) the change of CB Pharmas name from CB Pharma Acquisition Corp. to Origo Acquisition Corporation (Origo). In connection with the meeting, Fortress transferred 1,050,000 of its CB Pharma ordinary shares to Origo, retaining a holding of 265,000 Origo shares.
  • In May 2016, positive data from the Phase 1/2 study of CNDO-109-Activated Allogeneic Natural Killer (NK) Cells in patients with acute myeloid leukemia were presented in an oral session at the Innate Killer Summit 2016 in San Diego, CA.
  • In July 2016 Fortress stock was added to the Russell 2000 Index.

About Fortress Biotech

Fortress Biotech, Inc. (Fortress) is a biopharmaceutical company dedicated to acquiring, developing and commercializing novel pharmaceutical and biotechnology products. Fortress plans to develop and commercialize products both within Fortress and through subsidiary companies, also known as Fortress Companies.  Fortress intends to leverage its biopharmaceutical business expertise and drug development capabilities to help the Fortress Companies achieve their goals. Additionally, Fortress intends to provide funding and management services to each of the Fortress Companies and, from time to time, Fortress and the Fortress Companies will seek licensing, acquisitions, partnerships, joint ventures and/or public and private financings to accelerate and provide additional funding to support their research and development programs. For more information, visit www.fortressbiotech.com.

Forward-Looking Statements

This press release may contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Such statements include, but are not limited to, any statements relating to our growth strategy, potential acquisitions, product development programs and any other statements that are not historical facts. Forward-looking statements are based on managements current expectations and are subject to risks and uncertainties that could negatively affect our business, operating results, financial condition and stock price. Factors that could cause actual results to differ materially from those currently anticipated are: risks related to our growth strategy; our ability to continue to commercialize products; our ability to identify, acquire, close and integrate product candidates and companies successfully and on a timely basis; our need for substantial additional funds; our ability to obtain, perform under and maintain financing and strategic agreements and relationships; risks relating to the results of research and development activities; uncertainties relating to preclinical and clinical testing; our dependence on third-party suppliers; our ability to attract, integrate, and retain key personnel; the early stage of products under development; government regulation; patent and intellectual property matters; competition; and other risks described in our SEC filings. We expressly disclaim any obligation or undertaking to release publicly any updates or revisions to any forward looking statements contained herein to reflect any change in our expectations or any changes in events, conditions or circumstances on which any such statement is based, except as required by law.

 

FORTRESS BIOTECH, INC. AND SUBSIDIARIES 
Condensed Consolidated Balance Sheets 
(\\$ in thousands except for share and per share amounts) 
      
  June 30, December 31, 
   2016   2015  
  (Unaudited)   
 ASSETS    
 Current assets    
 Cash and cash equivalents\\$  71,336  \\$  98,182  
 Accounts receivable   967     -  
 Inventory   100     -  
 Other receivables - related party   2,570     156  
 Prepaid expenses and other current assets   1,579     1,599  
 Total current assets   76,552     99,937  
      
 Property and equipment, net   4,535     309  
 Restricted cash   14,586     14,586  
 Long-term investments, at fair value   766     2,485  
 Intangible asset - license   1,579     1,250  
 Other assets   44     43  
 Total assets\\$   98,062   \\$  118,610   
      
 LIABILITIES AND STOCKHOLDERS' EQUITY    
 Current liabilities    
 Accounts payable \\$  5,126  \\$  1,868  
 Accrued expenses    8,883     8,570  
 Interest payable   26     27  
 Derivative liabilities   302     114  
 Total current liabilities   14,337     10,579  
      
 Notes payable, long-term (net of debt discount of \\$412 and \\$835 at June 30, 2016 and December 31, 2015, respectively)   20,805    23,174  
 Convertible note, at fair value   1,000     -  
 Other long-term liabilities   3,706     584  
 Total liabilities   39,848      34,337   
      
 Commitments and contingencies    
      
 Stockholders' equity    
 Convertible Preferred stock, \\$.001 par value, 129,767 Series C shares authorized, 0 shares issued and outstanding as of June 30, 2016 and December 31, 2015, respectively   -     -  
 Common Stock, \\$.001 par value, 100,000,000 shares authorized, 48,668,630 and 47,147,032 shares issued and outstanding as of June 30, 2016 and December 31, 2015, respectively   49     47  
 Additional paid-in-capital  250,127   246,955  
 Accumulated deficit  (214,839)   (190,156) 
 Total stockholders' equity attributed to the Company   35,337     56,846  
      
 Non-controlling interests   22,877     27,427  
 Total stockholders' equity   58,214     84,273  
 Total liabilities and stockholders' equity\\$   98,062   \\$  118,610   
      

 

FORTRESS BIOTECH, INC. AND SUBSIDIARIES 
Condensed Consolidated Statements of Operations 
(\\$ in thousands except for share and per share amounts) 
(Unaudited) 
           
   For the Three Months Ended June 30, For the Six Months Ended June 30, 
    2016   2015   2016   2015  
 Product revenue, net \\$  981  \\$  -  \\$  1,364  \\$  -  
 Revenue - from a related party    1,249     -     1,526     500  
 Total revenue    2,230     -     2,890     500  
           
 Cost of goods sold - product revenue    324     -     324     -  
 Gross margin    1,906     -     2,566     500  
           
 Operating expenses         
 Research and development    6,347     2,411     14,100     4,066  
 Research and development licenses acquired    2,060     1,548     2,143     8,987  
 General and administrative    8,635     3,803     16,550     7,280  
 Total operating expenses    17,042     7,762     32,793     20,333  
 Loss from operations    (15,136)    (7,762)    (30,227)    (19,833) 
           
 Other income (expenses)         
 Interest income    77     74     152     156  
 Interest expense and financing fee    (529)    (352)    (1,149)    (683) 
 Change in fair value of derivative liabilities    -     -     (89)    -  
 Change in fair value of investments    (801)    1,622     (1,719)    1,407  
 Total other income (expenses)    (1,253)    1,344     (2,805)    880  
 Net loss    (16,389)    (6,418)    (33,032)    (18,953) 
           
 Less: net loss attributable to non-controlling interests    3,911     243     8,349     722  
 Net loss attributable to common stockholders \\$   (12,478) \\$   (6,175) \\$   (24,683) \\$   (18,231) 
           
 Basic and diluted net loss per common share \\$  (0.31) \\$  (0.16) \\$  (0.62) \\$  (0.47) 
           
 Weighted average common shares outstandingbasic and diluted    39,867,724     39,119,606     39,762,956     38,848,660