Galmed Pharmaceuticals Reports Full Year 2015 Financial Results and Provides Business Update

TEL AVIV, Israel, March 22, 2016 /PRNewswire/ -- Galmed Pharmaceuticals Ltd. (Nasdaq: GLMD) ("Galmed" or the "Company"), a clinical-stage biopharmaceutical company focused on the development of a once-daily, oral therapy for the treatment of liver diseases, today reported financial results for the three and twelve months ended December 31, 2015.  The Company will host a conference call and webcast today to discuss the financial results and to provide an update on current developments with respect to its clinical programs for Aramchol™.

Financial Summary – Full Year 2015 vs. Full Year 2014; 4Q15 vs. 4Q14:

• Net loss of $10.6 million, or $0.96 per share, for the twelve months ended December 31, 2015, compared with a net loss of $9.1 million, or $0.88 per share, for the twelve months ended December 31, 2014. During 2015, total R&D expenses increased $965 thousand, or 14% to $7.6 million, and total G&A expenses increased $768 thousand, or 31% to $3.2 million. In addition, 2015's net loss included $970 thousand of non-cash, stock-based compensation expense versus $601 thousand of non-cash stock-based compensation expense incurred during the corresponding period in 2014.
• For the quarter ended December 31, 2015, the net loss was $3.2 million, or $0.29 per share, which compares with $2.0 million, or $0.17 per share, for the same period in 2014. During the fourth quarter of 2015, total R&D expenses increased $1.7 million to $2.8 million, and total G&A expenses decreased $359 thousand to $569 thousand. This quarter's net loss included $160 thousand of non-cash, stock-based compensation income versus $131 thousand of non-cash stock-based compensation expense incurred during the corresponding period in 2014.
• Research and development expenses of $7.6 million for the twelve months ended December 31, 2015, compared with $6.7 million for the twelve months ended December 31, 2014. The increase primarily resulted from an increase in expenses related to the ARREST Study as the trial continues to progress, offset by a decrease in chemistry and formulation studies, due to the fact that, during 2014, the Company manufactured sufficient quantities of Aramchol™ for the ARREST Study.
• For the quarter ended December 31, 2015, research and development expenses totaled $2.8 million, which compares with $1.1 million for the same period in 2014. The increase primarily resulted from an increase in expenses related to the ARREST Study as the trial continues to progress.
• General and administrative expenses of $3.2 million for the twelve months ended December 31, 2015, compared with $2.5 million for the twelve months ended December 31, 2014. The increase primarily resulted from an increase in stock-based compensation expenses, salaries, benefits as well an increase in professional services and investor relations and business development expenses.
• For the quarter ended December 31, 2015, general and administrative expenses totaled $569 thousand, which compares with $928 thousand for the same period in 2014. The decrease primarily resulted from a decrease in stock-based compensation expenses and a decrease in investor relations and business development expenses.
• Total current assets totaled $23.4 million as of December 31, 2015, compared with $32.2 million as of December 31, 2014. The decrease in 2015 primarily resulted from our spend on ongoing clinical studies and operating activities. Galmed continues to expect that its cash balance will be sufficient to maintain its current operations into the second half of 2017.

"The Company's main focus remains the advancement of the ARREST Study, which is progressing generally as planned," stated Allen Baharaff, Galmed's President and Chief Executive Officer.  "At December 31, 2015, we had a total of 42 sites activated.  In the first quarter of 2016, we added another 5 sites; 3 in the US and 2 in Mexico, both high-screening countries.  During the second quarter 2016, we expect to activate another 30 sites, which include 13 sites in Italy, and 6 sites in Germany."

Mr. Baharaff continued, "Importantly, worldwide, we have now screened over 400 subjects for the ARREST Study.  As of March 20th, 2016, we had randomized 75 patients and have another 15 subjects that are eligible to be randomized.  In addition, 68 subjects are currently within the screening process, which normally takes between 6-8 weeks.  We expect the 120th patient to be randomized by the end of the second quarter, 2016, and the 240^th patient by the end of 2016.  Based on the current rate of screening and enrollment, we now expect results from the Interim Analysis to be available by December 2016, or early first-quarter 2017, and top-line data for the complete study by the first quarter, 2018, inclusive of the three-month follow-up period.  Now that we have six months of active global screening in the ARREST Study behind us, we feel very comfortable with our estimates."

"We also announced a couple weeks ago that we have now begun patient randomization in the ARRIVE Study, which is a proof-of-concept Investigator Initiated Trial to evaluate the safety and efficacy of Aramchol in up to 50 patients with HIV-associated lipodystrophy and NAFLD."

Mr. Baharaff concluded, "Continued execution on the ARREST Study, as well as fortifying our pipeline, are our clear priorities for this year."

Conference Call & Webcast:
Tuesday, March 22nd, 2016, 8:30 am Eastern Time / 5:30 am Pacific Time
Participant Dial-In Numbers:
Toll-Free:                              +1-888-430-8691
Toll/International:                   +1-719-325-2491
Conference ID:                       7194562
Webcast:                              http://galmedpharma.investorroom.com/events

Replay, available until April 5, 2016
Replay Dial-In Numbers:
Toll-Free:                              +1-877-870-5176
Toll/International:                   +1-858-384-5517
Passcode:                            7194562

About Galmed Pharmaceuticals Ltd.:
Galmed is a clinical-stage biopharmaceutical company focused on the development of a novel, once-daily, oral therapy for the treatment of liver diseases utilizing its proprietary first-in-class family of synthetic fatty-acid/bile-acid conjugates, or FABACs.  Galmed believes that its product candidate, Aramchol™, has the potential to be a disease modifying treatment for fatty liver disorders, including NASH, which is a chronic disease that Galmed believes constitutes a large unmet medical need.  Galmed is currently conducting the ARREST Study, a multicenter, randomized, double blind, placebo-controlled Phase IIb clinical study designed to evaluate the efficacy and safety of Aramchol™ in subjects with NASH, who are overweight or obese, and who are pre-diabetic or type-II-diabetic.  More information about the ARREST Study may be found on ClinicalTrials.gov identifier: NCT02279524.

Forward-Looking Statements:
This press release may include forward-looking statements.  Forward-looking statements may include, but are not limited to, statements relating to Galmed's objectives, plans and strategies, as well as statements, other than historical facts, that address activities, events or developments that Galmed intends, expects, projects, believes or anticipates will or may occur in the future.  These statements are often characterized by terminology such as "believes," "hopes," "may," "anticipates," "should," "intends," "plans," "will," "expects," "estimates," "projects," "positioned," "strategy" and similar expressions and are based on assumptions and assessments made in light of management's experience and perception of historical trends, current conditions, expected future developments and other factors believed to be appropriate.  Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statements.  Applicable risks and uncertainties include those identified under the heading "Risk Factors" included in Galmed's most recent Annual Report on Form 20-F filed with the Securities and Exchange Commission, or the SEC, on March 22, 2016, and in other filings that Galmed has made and may make with the SEC in the future.  The forward-looking statements contained in this press release are made as of the date of this press release and reflect Galmed's current views with respect to future events, and Galmed does not undertake and specifically disclaims any obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

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SOURCE Galmed Pharmaceuticals Ltd.

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