| 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 | -22.00K | -37.00K | -33.00K | -32.00K | -41.00K | -36.00K |
| EBITDA | -30.17M | -41.47M | -38.24M | -37.71M | -30.00M | -23.34M |
| Net Income | -37.30M | -47.05M | -41.07M | -38.78M | -30.53M | -23.46M |
Balance Sheet | ||||||
| Total Assets | 12.87M | 17.50M | 28.20M | 21.29M | 41.83M | 29.60M |
| Cash, Cash Equivalents and Short-Term Investments | 11.53M | 15.12M | 25.66M | 18.59M | 39.65M | 27.14M |
| Total Debt | 122.31M | 106.25M | 71.81M | 39.87M | 29.06M | 44.00K |
| Total Liabilities | 138.17M | 120.56M | 88.44M | 53.48M | 39.21M | 5.41M |
| Stockholders Equity | -125.30M | -103.07M | -60.24M | -32.19M | 2.62M | 24.19M |
Cash Flow | ||||||
| Free Cash Flow | -30.62M | -41.77M | -32.97M | -31.06M | -24.31M | -20.60M |
| Operating Cash Flow | -30.62M | -41.77M | -32.97M | -31.06M | -24.31M | -20.60M |
| Investing Cash Flow | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Financing Cash Flow | 15.09M | 31.23M | 40.03M | 10.00M | 36.81M | 263.00K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
55 Neutral | $401.65M | -5.57 | -32.21% | ― | ― | 60.40% | |
55 Neutral | $609.56M | -1.17 | -50.23% | 14.68% | ― | 89.16% | |
52 Neutral | $953.61M | -6.67 | ― | ― | ― | 12.32% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
46 Neutral | $225.74M | -1.87 | -46.09% | ― | -80.88% | -388.61% | |
44 Neutral | $206.33M | -5.41 | ― | ― | ― | 18.82% | |
44 Neutral | $167.14M | -0.98 | -96.44% | ― | ― | 46.68% |
On December 19, 2025, Galectin Therapeutics reported that the U.S. Food and Drug Administration provided a written response to the company’s Type C meeting request on the development program for belapectin, leading the company to believe there is regulatory alignment on the proposed patient population for a future registration trial in MASH cirrhosis. The company plans a follow-up Type C meeting to finalize remaining trial design details and to present new biomarker data, viewing this interaction as a key step toward a pivotal Phase 3 study and an opportunity to integrate input from external key opinion leaders, which it sees as important for advancing belapectin’s clinical strategy. Separately on December 19, 2025, Galectin Therapeutics entered into a new unsecured, convertible line of credit of up to $10 million with its chairman, Richard E. Uihlein, and extended the maturity of all his existing convertible credit lines and notes to June 30, 2027, a move that, together with existing cash, is expected to fund operations through at least March 2027 and underscores continued insider financial support as the company progresses its late-stage liver disease program.
The most recent analyst rating on (GALT) stock is a Buy with a $11.00 price target. To see the full list of analyst forecasts on Galectin Therapeutics stock, see the GALT Stock Forecast page.
At the 2025 Annual Meeting of Stockholders on December 3, 2025, Galectin Therapeutics‘ stockholders elected the nominated directors and approved a non-binding advisory resolution on executive compensation. They also ratified Cherry Bekaert LLP as the independent registered public accounting firm for the year ending December 31, 2025. The board decided to conduct advisory votes on executive compensation every three years.
The most recent analyst rating on (GALT) stock is a Buy with a $6.00 price target. To see the full list of analyst forecasts on Galectin Therapeutics stock, see the GALT Stock Forecast page.
On December 3, 2025, Galectin Therapeutics presented compelling results from its NAVIGATE trial at its Annual Meeting of Stockholders. The trial focused on belapectin’s efficacy in treating MASH cirrhosis and portal hypertension, showing significant benefits in reducing liver stiffness and varices compared to placebo. The company highlighted the trial’s adaptive design and the decision to unblind data in 2024, which led to extensive data analysis throughout 2025. Key findings included belapectin’s impact on fibrosis and inflammation markers, with no drug-related serious adverse events reported. The results reinforce belapectin’s potential to change the treatment landscape for patients with no FDA-approved therapy, and Galectin is anticipating FDA feedback and exploring strategic opportunities to maximize program value.
The most recent analyst rating on (GALT) stock is a Buy with a $6.00 price target. To see the full list of analyst forecasts on Galectin Therapeutics stock, see the GALT Stock Forecast page.
On November 10, 2025, Galectin Therapeutics announced the presentation of its NAVIGATE trial results at the AASLD 2025 Annual Meeting. The Phase 2b trial evaluated belapectin, a galectin-3 inhibitor, in patients with compensated MASH cirrhosis and portal hypertension. The results demonstrated belapectin’s potential as a disease-modifying therapy, showing significant antifibrotic effects and a reduction in the incidence of new varices compared to placebo. These findings suggest a promising therapeutic option for patients with limited treatment choices, and the company is focused on advancing regulatory discussions and strategic partnerships to further develop belapectin.
The most recent analyst rating on (GALT) stock is a Buy with a $6.00 price target. To see the full list of analyst forecasts on Galectin Therapeutics stock, see the GALT Stock Forecast page.