| Breakdown | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 0.00 | 0.00 | 2.00M | 0.00 | 0.00 |
| Gross Profit | 0.00 | 0.00 | 2.00M | 0.00 | 0.00 |
| EBITDA | -56.89M | -45.57M | -30.74M | -31.05M | -23.72M |
| Net Income | -51.04M | -45.57M | -27.88M | -30.50M | -24.44M |
Balance Sheet | |||||
| Total Assets | 116.48M | 160.26M | 96.72M | 33.03M | 59.03M |
| Cash, Cash Equivalents and Short-Term Investments | 113.12M | 151.25M | 94.90M | 32.34M | 56.73M |
| Total Debt | 78.00K | 78.00K | 65.00K | 211.00K | 348.00K |
| Total Liabilities | 5.10M | 4.45M | 5.65M | 219.98M | 217.29M |
| Stockholders Equity | 111.38M | 155.81M | 91.06M | -186.95M | -158.26M |
Cash Flow | |||||
| Free Cash Flow | -45.65M | -42.44M | -23.77M | -24.49M | -21.71M |
| Operating Cash Flow | -45.65M | -42.44M | -23.77M | -24.49M | -21.71M |
| Investing Cash Flow | 4.56M | -61.68M | 12.58M | -32.01M | 0.00 |
| Financing Cash Flow | 275.00K | 104.82M | 86.17M | -73.00K | 9.74M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
59 Neutral | $120.79M | -6.32 | 17.78% | ― | ― | ― | |
57 Neutral | $486.00M | -1.84 | -46.34% | ― | ― | 14.33% | |
55 Neutral | $485.83M | -2.96 | -39.83% | ― | -71.42% | -248.91% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $161.52M | -3.75 | -40.85% | ― | ― | -38.23% | |
50 Neutral | $146.30M | -3.23 | -114.26% | ― | -17.87% | 14.42% | |
50 Neutral | $294.57M | -1.33 | -107.14% | ― | ― | -17.21% |
Sagimet Biosciences reported its fourth-quarter and full-year 2025 results on March 11, 2026, highlighting clinical progress across its MASH and acne portfolios and solid liquidity of $113.1 million in cash, cash equivalents and marketable securities at year-end. The company completed a Phase 1 pharmacokinetic trial of denifanstat combined with thyroid hormone receptor beta agonist resmetirom with no safety signals and plans to advance this combination into a Phase 2 proof-of-concept trial in F4 MASH in the second half of 2026, while continuing a Phase 1 trial of acne-targeted FASN inhibitor TVB-3567.
In parallel, Sagimet strengthened its combination strategy via a global, exclusive license to innovative resmetirom active pharmaceutical ingredient forms from TAPI and benefited from partner Ascletis’ positive 52-week Phase 3 acne data and China NMPA acceptance of a New Drug Application for denifanstat in moderate to severe acne. Financially, 2025 research and development expenses were $39.1 million and net loss widened to $51.0 million, reflecting an intensified development program that could enhance the company’s position in high-need liver and dermatology markets if upcoming Phase 2 trials and regulatory pathways progress as planned.
The most recent analyst rating on (SGMT) stock is a Buy with a $37.00 price target. To see the full list of analyst forecasts on Sagimet Biosciences, Inc. Class A stock, see the SGMT Stock Forecast page.
On February 2, 2026, Sagimet Biosciences reported that its Chinese license partner Ascletis Pharma released positive topline data from a 52-week Phase 3 program of denifanstat (ASC40) in patients with moderate to severe acne, including an open-label extension trial evaluating long-term safety. In the multi-center ASC40-304 study, 240 patients who had completed a prior 12-week randomized Phase 3 trial received once-daily oral denifanstat 50 mg for up to 40 additional weeks; treatment was generally well tolerated, with only mild to moderate treatment-related adverse events, low rates of common side effects such as dry eye and dry skin, no denifanstat-related serious adverse events, and no permanent discontinuations attributed to the drug. Patients experienced further improvements across all key efficacy measures—including Investigator’s Global Assessment response rates and reductions in total and inflammatory lesion counts—beyond those seen at 12 weeks, strengthening the clinical case for FASN inhibition as a novel mechanism in acne and supporting Sagimet’s broader strategy to advance denifanstat and next-generation FASN inhibitors across dermatologic and metabolic indications.
The most recent analyst rating on (SGMT) stock is a Buy with a $26.00 price target. To see the full list of analyst forecasts on Sagimet Biosciences, Inc. Class A stock, see the SGMT Stock Forecast page.
On 18 December 2025, Sagimet Biosciences updated its investor presentation and issued a press release reporting positive results from a Phase 1 pharmacokinetic trial evaluating a combination of its FASN inhibitor denifanstat with the thyroid hormone receptor beta agonist resmetirom, a pairing supported by preclinical evidence of synergistic effects in MASH. The refreshed materials highlight denifanstat’s progress in MASH, where a Phase 2b trial previously met histology primary and multiple secondary endpoints and the program has FDA Breakthrough Therapy designation with Phase 3 readiness, as well as the completion of a Phase 1 hepatic impairment study and the new Phase 1 combination PK data that pave the way for a planned Phase 2 trial in MASH cirrhosis (F4) in the second half of 2026. The company also underscores growing momentum in dermatology, with licensee Ascletis having reported that a Phase 3 acne trial of denifanstat in China met all primary and secondary endpoints and that a new drug application for moderate to severe acne was accepted by China’s NMPA in December 2025, while Sagimet advances TVB-3567 in a first-in-human Phase 1 acne study, collectively strengthening its clinical pipeline and reinforcing its strategic positioning in metabolic and inflammatory diseases.
The most recent analyst rating on (SGMT) stock is a Buy with a $26.00 price target. To see the full list of analyst forecasts on Sagimet Biosciences, Inc. Class A stock, see the SGMT Stock Forecast page.
Sagimet Biosciences Inc. announced its entrance into a license agreement with TAPI Technology & API Services, a subsidiary of Teva Pharmaceutical Industries Ltd., on December 17, 2025. This collaboration grants Sagimet a global, exclusive license to TAPI’s innovative resmetirom active pharmaceutical ingredient (API), supporting the development of a fixed-dose combination (FDC) product featuring denifanstat and resmetirom. The program aims to address critical unmet needs for cirrhosis patients affected by F4-stage MASH. This move marks a significant step forward for Sagimet’s research and development efforts as it aligns with preclinical data showing synergy in treating liver diseases, positioning Sagimet for further advancement in the field.
The most recent analyst rating on (SGMT) stock is a Buy with a $26.00 price target. To see the full list of analyst forecasts on Sagimet Biosciences, Inc. Class A stock, see the SGMT Stock Forecast page.