| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | 0.00 | -83.00K | -31.00K | -35.00K | -42.00K | -39.00K |
| EBITDA | -7.09M | -7.42M | -6.87M | -17.62M | -32.84M | -30.17M |
| Net Income | -8.70M | -7.52M | -6.91M | -18.57M | -31.95M | -27.61M |
Balance Sheet | ||||||
| Total Assets | 21.58M | 18.50M | 16.63M | 16.56M | 36.60M | 52.38M |
| Cash, Cash Equivalents and Short-Term Investments | 19.05M | 15.33M | 12.64M | 13.79M | 34.81M | 50.89M |
| Total Debt | 0.00 | 0.00 | 41.00K | 44.00K | 229.00K | 216.00K |
| Total Liabilities | 2.47M | 2.17M | 2.75M | 3.14M | 6.11M | 8.23M |
| Stockholders Equity | 19.11M | 16.33M | 13.88M | 13.42M | 30.50M | 44.15M |
Cash Flow | ||||||
| Free Cash Flow | -6.34M | -5.88M | -6.14M | -18.50M | -32.90M | -26.33M |
| Operating Cash Flow | -6.34M | -5.88M | -6.14M | -18.50M | -32.89M | -26.29M |
| Investing Cash Flow | -8.35M | -1.11M | 800.00K | 17.56M | 11.46M | 16.54M |
| Financing Cash Flow | 8.29M | 8.79M | 6.18M | 70.00K | 17.37M | 768.00K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
52 Neutral | $7.18M | -0.02 | -655.85% | ― | ― | -228.89% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
44 Neutral | $4.56M | -0.24 | -46.34% | ― | ― | 70.71% | |
44 Neutral | $8.24M | -0.13 | ― | ― | ― | 87.42% | |
41 Neutral | $3.92M | -0.02 | -370.95% | ― | 12.45% | -544.23% | |
40 Underperform | $3.79M | -0.06 | ― | ― | -41.05% | 57.35% |
On December 8, 2025, Galmed Pharmaceuticals announced the acceptance of a late-breaking abstract for its lead drug candidate, Aramchol, to be presented at the HEP-DART 2025 meeting. The abstract highlights the potential of Aramchol in combination with regorafenib to enhance treatment efficacy in hepatocellular carcinoma and other gastrointestinal cancers. This development has led to the initiation of a Phase 1/2 clinical trial by VCU Massey Comprehensive Cancer Center, with enrollment planned for 2026. The successful presentation and subsequent clinical trial could significantly expand Galmed’s oncology pipeline and create value for stakeholders.
On December 4, 2025, Galmed Pharmaceuticals announced the grant of a new use patent in South Korea for a combination therapy involving its lead compound, Aramchol, and Madrigal Pharmaceuticals’ Rezdiffra (Resmetirom) for treating non-alcoholic steatohepatitis (MASH) and liver fibrosis. This patent, which extends Aramchol’s protection worldwide until July 2042, marks a significant step in the company’s strategy to lead in the NASH/MASH combination therapy market. The announcement underscores the industry’s shift towards combination therapies to address complex diseases like MASH, highlighting Aramchol’s excellent safety and tolerability as a key advantage.
On December 1, 2025, Galmed Pharmaceuticals issued a CEO letter to shareholders highlighting the company’s recent achievements and future plans. The company has expanded its therapeutic focus beyond liver disease, generating new data supporting Aramchol’s broader clinical development path in oncology and cardiometabolic indications. Galmed maintains a strong cash position with $19.2 million and minimal debt, allowing it to continue its development plans without aggressive capital raises. The company is advancing Aramchol in combination therapies for MASH and gastrointestinal oncology, with plans for further clinical trials. These developments position Galmed for significant growth opportunities and potential FDA approval, enhancing its market presence and stakeholder value.
Galmed Pharmaceuticals announced its financial results for the third quarter of 2025, highlighting a net loss of approximately $2.0 million, an increase in research and development expenses, and a decrease in general and administrative expenses compared to the same period in 2024. The company also reported significant progress in its research collaborations, including promising results from a study on Aramchol’s effectiveness in combating drug resistance in gastrointestinal cancers, and a successful Phase 1 study of Aramchol Meglumine, which could enhance its market positioning and stakeholder confidence.
On November 18, 2025, Galmed Pharmaceuticals announced significant top-line results from its AM-001 Phase 1 Bioavailability Study of Aramchol meglumine. The study revealed that Aramchol meglumine granules have a considerably higher bioavailability compared to Aramchol free acid tablets, with potential implications for improved patient adherence and reduced drug costs. These findings support the advancement of Aramchol meglumine into Phase 2 oncology studies planned for the first half of 2026, marking a pivotal step in the drug’s development and commercialization strategy.
Galmed Pharmaceuticals announced on November 17, 2025, the top-line results of their oncology mechanism of action studies involving a three-drug combination of Aramchol, Stivarga®, and Metformin, which demonstrated significant enhancement in killing gastrointestinal tumor cells both in vivo and in vitro. This combination has the potential to serve as a new fixed-dose treatment and a life-cycle IP strategy for Bayer’s Stivarga® as its patents near expiration, with plans to enter Phase 1b clinical trials in early 2026, potentially expanding Galmed’s pipeline and creating value for stakeholders.
On October 29, 2025, Galmed Pharmaceuticals Ltd. held its Annual General Meeting of Shareholders, where all proposals presented were approved by the requisite majority in accordance with Israeli law. This approval signifies continued shareholder support for the company’s strategic direction and operational plans, potentially impacting its market position and stakeholder confidence positively.
On October 28, 2025, Galmed Pharmaceuticals Ltd. held its Annual General Meeting of Shareholders, which was adjourned due to a lack of quorum. The meeting is scheduled to reconvene on October 29, 2025, at the same location. This adjournment may impact the company’s ability to address shareholder concerns and make timely decisions, potentially affecting its strategic direction and stakeholder confidence.