| Breakdown | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 67.00M | 28.57M | 20.20M | 80.07M | 765.00K |
| Gross Profit | 66.70M | 28.22M | 19.95M | 79.91M | 563.00K |
| EBITDA | 8.35M | -22.24M | -25.80M | 34.91M | -73.03M |
| Net Income | 1.51M | -28.89M | -23.72M | 67.26M | -101.22M |
Balance Sheet | |||||
| Total Assets | 151.42M | 173.87M | 215.54M | 281.72M | 198.61M |
| Cash, Cash Equivalents and Short-Term Investments | 81.79M | 77.79M | 140.55M | 258.76M | 171.03M |
| Total Debt | 62.13M | 70.18M | 75.28M | 74.23M | 185.69M |
| Total Liabilities | 82.20M | 105.92M | 121.01M | 162.62M | 214.78M |
| Stockholders Equity | 69.22M | 67.95M | 94.53M | 119.10M | -16.16M |
Cash Flow | |||||
| Free Cash Flow | 14.22M | -57.92M | -72.64M | 99.38M | -97.27M |
| Operating Cash Flow | 15.20M | -55.43M | -72.64M | 99.92M | -96.37M |
| Investing Cash Flow | -1.04M | 2.23M | -46.27M | -3.38M | -966.00K |
| Financing Cash Flow | -10.57M | -5.10M | -3.79M | -8.92M | -8.26M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
58 Neutral | $490.84M | ― | -38.87% | ― | ― | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $206.09M | -4.79 | -51.06% | ― | -44.94% | -274.42% | |
42 Neutral | $324.56M | ― | -43.95% | ― | ― | ― | |
40 Underperform | $475.71M | ― | ― | ― | ― | 10.15% | |
39 Underperform | $708.83M | -2.01 | -77.83% | ― | ― | 43.16% |
On October 30, 2025, GENFIT announced its decision to voluntarily delist its American Depositary Shares (ADSs) from the Nasdaq Global Select Market, effective before November 20, 2025. This strategic move aims to simplify the company’s corporate structure and enhance operational efficiency, while maintaining its primary listing on Euronext Paris. The delisting will not affect GENFIT’s commitment to high standards of corporate governance and transparency, nor will it impact its accounting standards. The company will continue to comply with French and European financial regulations, and the delisting process involves filing necessary forms with the U.S. Securities and Exchange Commission.
On October 28, 2025, GENFIT announced its participation in the upcoming AASLD The Liver Meeting® 2025, where it will present new data on its ACLF pipeline, including the lead program G1090N, and other programs like SRT-015 and CLM-022. The company will also present real-world evidence and biomarker insights in cirrhosis. Ipsen, a partner of GENFIT, will present data on Iqirvo® in rare cholestatic liver diseases, highlighting its potential to address disease progression and symptom burden. These presentations underscore GENFIT’s commitment to advancing treatments for liver diseases and enhancing its industry positioning.
On September 22, 2025, GENFIT S.A. released its Half-Year Business and Financial Report for the period ending June 30, 2025. The report details the company’s ongoing R&D programs, including developments in their ACLF franchise and other serious diseases. The report also highlights the company’s strategic outlook and financial performance, providing insights into GENFIT’s industry positioning and potential implications for stakeholders.
On September 22, 2025, GENFIT announced its first-half 2025 financial results, highlighting a cash position of €107.5 million as of June 30, 2025, and significant revenue from milestone payments related to its drug Iqirvo® (elafibranor) in Europe. The company decided to discontinue its VS-01 program for ACLF due to safety concerns but remains committed to other ACLF-related programs and continues to explore new therapeutic avenues. The withdrawal of a key competitor from the U.S. market is expected to benefit Iqirvo® sales. GENFIT’s strategic moves, including the acquisition of full rights for GNS561 and a royalty financing agreement, have extended its cash runway beyond 2028, providing financial stability and opportunities for further development initiatives.
On September 19, 2025, GENFIT announced the discontinuation of its VS-01 program for Acute-on-Chronic Liver Failure (ACLF) due to safety concerns, specifically a serious adverse event in the UNVEIL-IT® clinical trial. The company will refocus VS-01 development on Urea Cycle Disorder (UCD), a condition with significant unmet medical needs. This strategic shift is expected to reduce operating expenses and extend GENFIT’s cash runway beyond 2028, while allowing the company to explore new approaches in ACLF care. GENFIT remains committed to its other ACLF programs and aims to deliver positive results from its pipeline, including safety data for G1090N by year-end.