| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 2.93M | 3.75M | 140.14M | 5.09M | 13.16M | 0.00 |
| Gross Profit | 2.93M | 3.75M | 124.52M | 4.46M | 12.85M | -303.00K |
| EBITDA | 2.15M | -18.58M | 70.89M | -59.91M | -32.91M | -55.65M |
| Net Income | -25.30M | -21.29M | 67.04M | -62.81M | -32.87M | -55.19M |
Balance Sheet | ||||||
| Total Assets | 51.07M | 90.64M | 128.41M | 87.81M | 119.84M | 102.54M |
| Cash, Cash Equivalents and Short-Term Investments | 38.01M | 59.30M | 74.36M | 73.50M | 104.48M | 93.04M |
| Total Debt | 2.28M | 16.27M | 15.08M | 48.60M | 43.63M | 19.84M |
| Total Liabilities | 14.64M | 35.57M | 55.45M | 84.58M | 78.58M | 79.78M |
| Stockholders Equity | 36.43M | 55.08M | 72.96M | 3.23M | 41.26M | 22.76M |
Cash Flow | ||||||
| Free Cash Flow | -33.59M | -24.01M | 60.16M | -79.89M | -55.73M | -49.36M |
| Operating Cash Flow | -33.59M | -24.01M | 60.16M | -79.88M | -54.56M | -49.35M |
| Investing Cash Flow | 33.51M | 6.15M | -34.88M | -27.39M | -1.17M | 6.47M |
| Financing Cash Flow | -14.21M | -139.00K | -36.72M | 48.60M | 67.12M | 94.00M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $39.79M | -12.47 | -13.08% | ― | 12.21% | 69.91% | |
48 Neutral | $21.11M | -0.76 | -50.23% | ― | -15.61% | -68.96% | |
47 Neutral | $13.54M | -29.32 | 0.27% | ― | 75.19% | ― | |
46 Neutral | $26.45M | -1.11 | -53.29% | ― | -65.77% | 38.61% | |
44 Neutral | $36.84M | ― | -16.67% | ― | -23.60% | -179.33% | |
42 Neutral | $9.13M | -2.21 | -93.87% | ― | -0.74% | 81.49% |
On October 14, 2025, SCYNEXIS and GSK signed a binding memorandum of understanding to amend their exclusive license agreement, resolving a prior disagreement over the Phase 3 MARIO study of ibrexafungerp. SCYNEXIS agreed to terminate the MARIO Study and will receive a $22 million payment from GSK, along with an additional $2.3 million for wind-down activities. GSK remains committed to the commercialization of BREXAFEMME® for VVC and rVVC, with plans to engage with the FDA in 2026 for its U.S. market relaunch. The agreement maintains the potential milestones and royalties for SCYNEXIS, excluding those related to the MARIO Study.