NORCROSS, Ga., Aug. 13, 2024 (GLOBE NEWSWIRE) -- Galectin Therapeutics, Inc. (NASDAQ: GALT), the leading developer of therapeutics that target galectin proteins, today reported financial results and provided a business update for the quarter ended June 30, 2024.
Joel Lewis, Chief Executive Officer and President of Galectin Therapeutics, said, “We continued to advance the NAVIGATE Phase 2b/3 trial of belapectin in the first half of 2024. We believe that belapectin can potentially offer a new medical treatment option for the increasing number of patients affected with MASH associated liver cirrhosis and portal hypertension that represents a significant unmet medical need, and we are excited for the planned upcoming interim analysis in December 2024.”
Khurram Jamil, M.D., Chief Medical Officer, added, “We were pleased to share the important data from our belapectin program demonstrating that collagen content in liver biopsies of MASH cirrhotic patients does not correlate with portal pressure, which is a key marker of disease progression at the EASL 2024 congress. These insights underscore the importance of truly understanding the overall health of the liver and highlights the effectiveness of endoscopies in determining that.”
Belapectin Program Q2 2024 and Recent Highlights
Belapectin is a complex carbohydrate drug that targets galectin-3, a critical protein in the pathogenesis of MASH and fibrosis.
MASH Cirrhosis
Q2 2024 Financial Highlights
About Galectin Therapeutics
Galectin Therapeutics is dedicated to developing novel therapies to improve the lives of patients with chronic liver disease and cancer. Galectin’s lead drug belapectin is a carbohydrate-based drug that inhibits the galectin-3 protein, which is directly involved in multiple inflammatory, fibrotic, and malignant diseases, for which it has Fast Track designation by the U.S. Food and Drug Administration. The lead development program is in metabolic dysfunction-associated steatohepatitis (MASH, formerly known as nonalcoholic steatohepatitis, or NASH) with cirrhosis, the most advanced form of MASH-related fibrosis. Liver cirrhosis is one of the most pressing medical needs and a significant drug development opportunity. Additional development programs are in treatment of combination immunotherapy for advanced head and neck cancers and other malignancies. Advancement of these additional clinical programs is largely dependent on finding a suitable partner. Galectin seeks to leverage extensive scientific and development expertise as well as established relationships with external sources to achieve cost-effective and efficient development. Additional information is available at www.galectintherapeutics.com.
Forward Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements relate to future events or future financial performance, and use words such as “may,” “estimate,” “could,” “expect,” “look forward,” “believe,” “hope” and others. They are based on management’s current expectations and are subject to factors and uncertainties that could cause actual results to differ materially from those described in the statements. These statements include those regarding the hope that Galectin’s development program for belapectin will lead to the first therapy for the treatment of MASH, formerly known as NASH, with cirrhosis and those regarding the hope that our lead compounds will be successful in cancer immunotherapy and in other therapeutic indications. Factors that could cause actual performance to differ materially from those discussed in the forward-looking statements include, among others, that trial endpoints required by the FDA may not be achieved; Galectin may not be successful in developing effective treatments and/or obtaining the requisite approvals for the use of belapectin or any of its other drugs in development; the Company may not be successful in scaling up manufacturing and meeting requirements related to chemistry, manufacturing and control matters; the Company’s current clinical trial and any future clinical studies may not produce positive results in a timely fashion, if at all, and could require larger and longer trials, which would be time consuming and costly; plans regarding development, approval and marketing of any of Galectin’s drugs are subject to change at any time based on the changing needs of the Company as determined by management and regulatory agencies; regardless of the results of any of its development programs, Galectin may be unsuccessful in developing partnerships with other companies or raising additional capital that would allow it to further develop and/or fund any studies or trials. Galectin has incurred operating losses since inception, and its ability to successfully develop and market drugs may be impacted by its ability to manage costs and finance continuing operations. For a discussion of additional factors impacting Galectin’s business, see the Company’s Annual Report on Form 10-K for the year ended December 31, 2023, and subsequent filings with the SEC. You should not place undue reliance on forward-looking statements. Although subsequent events may cause its views to change, management disclaims any obligation to update forward-looking statements.
Company Contact:
Jack Callicutt, Chief Financial Officer
(678) 620-3186
This email address is being protected from spambots. You need JavaScript enabled to view it.
Investors Relations Contacts:
Kevin Gardner
This email address is being protected from spambots. You need JavaScript enabled to view it.
Chris Calabrese
This email address is being protected from spambots. You need JavaScript enabled to view it.
Galectin Therapeutics and its associated logo is a registered trademark of Galectin Therapeutics Inc. Belapectin is the USAN assigned name for Galectin Therapeutics’ galectin-3 inhibitor belapectin.
Condensed Consolidated Statements of Operations
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||
| 2024 | 2023 | 2024 | 2023 | |||||||||
| (in thousands, except per share data) | ||||||||||||
| Operating expenses: | ||||||||||||
| Research and development | $ | 9,813 | $ | 7,371 | $ | 17,867 | $ | 16,170 | ||||
| General and administrative | 1,478 | 1,632 | 3,072 | 3,175 | ||||||||
| Total operating expenses | 11,291 | 9,003 | 20,939 | 19,345 | ||||||||
| Total operating loss | (11,291) | (9,003) | (20,939) | (19,345) | ||||||||
| Other income (expense): | ||||||||||||
| Interest income | 80 | 50 | 160 | 93 | ||||||||
| Interest expense | (1,269) | (650) | (2,321) | (1,110) | ||||||||
| Change in fair value of derivative | 109 | 489 | (760) | (279) | ||||||||
| Total other income | (1,080) | (111) | (2,921) | (1,296) | ||||||||
| Net loss | $ | (12,371) | $ | (9,114) | $ | (23,860) | $ | (20,641) | ||||
| Preferred stock dividends | (64) | (63) | (72) | (63) | ||||||||
| Warrant modification | ||||||||||||
| Net loss applicable to common stock | $ | (12,435) | $ | (9,177) | $ | (23,932) | $ | (20,704) | ||||
| Basic and diluted net loss per share | $ | (0.20) | $ | (0.15) | $ | (0.38) | $ | (0.35) | ||||
| Shares used in computing basic and diluted net loss per share | 62,233 | 59,582 | 62,192 | 59,531 | ||||||||
Condensed Consolidated Balance Sheet Data
| June 30, 2024 | December 31, 2023 | |||||
| (in thousands) | ||||||
| Cash and cash equivalents | $ | 25,598 | $ | 25,660 | ||
| Total assets | 27,655 | 28,200 | ||||
| Total current liabilities | 14,617 | 15,676 | ||||
| Total liabilities | 109,802 | 88,441 | ||||
| Total redeemable, convertible preferred stock | 1,723 | 1,723 | ||||
| Total stockholders’ equity (deficit) | $ | (83,870) | $ | (61,964) | ||
| Last Trade: | US$2.78 |
| Daily Change: | 0.06 2.21 |
| Daily Volume: | 151,691 |
| Market Cap: | US$173.140M |
November 18, 2024 November 14, 2024 October 15, 2024 September 03, 2024 June 04, 2024 | |
Astria Therapeutics is a biopharmaceutical company, and our mission is to bring life-changing therapies to patients and families affected by rare and niche allergic and immunological diseases. Our lead program, STAR-0215, is a monoclonal antibody inhibitor of plasma kallikrein in clinical development...
CLICK TO LEARN MORE
Terns Pharmaceuticals is a clinical-stage biopharmaceutical company developing a portfolio of small-molecule product candidates to address serious diseases, including oncology and obesity. Terns’ pipeline contains three clinical stage development programs including GLP-1 receptor...
CLICK TO LEARN MORE
