| Breakdown | TTM | Dec 2025 | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 64.81M | ― | 65.32M | 67.64M | 79.20M | 86.16M |
| Gross Profit | 64.81M | ― | 65.32M | 67.64M | 79.20M | 86.16M |
| EBITDA | -82.41M | ― | -70.78M | -104.51M | -123.48M | -119.22M |
| Net Income | -92.01M | ― | -81.89M | -116.05M | -133.82M | -121.75M |
Balance Sheet | ||||||
| Total Assets | 301.03M | ― | 280.73M | 376.65M | 462.27M | 380.59M |
| Cash, Cash Equivalents and Short-Term Investments | 204.11M | ― | 188.86M | 248.19M | 369.91M | 249.23M |
| Total Debt | 207.10M | ― | 201.06M | 226.06M | 222.44M | 26.69M |
| Total Liabilities | 221.75M | ― | 216.01M | 247.84M | 245.54M | 59.26M |
| Stockholders Equity | 79.28M | ― | 64.72M | 128.81M | 216.74M | 321.33M |
Cash Flow | ||||||
| Free Cash Flow | -43.57M | ― | -32.17M | -96.71M | -112.21M | -86.91M |
| Operating Cash Flow | -23.18M | ― | -19.27M | -78.76M | -103.15M | -84.78M |
| Investing Cash Flow | 57.12M | ― | 40.35M | 58.23M | -53.58M | 54.90M |
| Financing Cash Flow | -25.51M | ― | -26.62M | -27.63M | 198.13M | 20.03M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
55 Neutral | $453.43M | -4.09 | -84.63% | ― | -3.42% | 30.03% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $305.63M | -1.39 | -54.43% | ― | -100.00% | 37.10% | |
50 Neutral | $287.21M | 4.55 | 75.90% | ― | ― | ― | |
42 Neutral | $398.84M | -5.53 | -32.21% | ― | ― | 60.40% | |
39 Underperform | $752.17M | -1.44 | -50.23% | 14.68% | ― | 89.16% | |
33 Underperform | $292.41M | -1.20 | -104.35% | ― | ― | 20.71% |
On September 30, 2025, Enanta Pharmaceuticals announced a public offering of 6,500,000 shares of its common stock at $10.00 per share, with an option for underwriters to purchase an additional 975,000 shares. The expected net proceeds of approximately $60.6 million will support the company’s operations, with the offering set to close on October 2, 2025, subject to customary conditions.
On September 29, 2025, Enanta Pharmaceuticals announced positive topline results from its Phase 2b study of zelicapavir in high-risk adults for the treatment of respiratory syncytial virus (RSV). The study demonstrated a clinically meaningful reduction in symptom duration, supporting further development towards a Phase 3 trial. This advancement positions Enanta strategically in the RSV treatment market, potentially addressing significant unmet needs for high-risk populations, including older adults and those with chronic heart or lung diseases.
On September 29, 2025, Enanta Pharmaceuticals announced positive topline data from its Phase 2b study of zelicapavir for treating respiratory syncytial virus (RSV) in high-risk adults. The study showed that zelicapavir, a novel N-protein inhibitor, significantly improved the time to complete resolution of RSV symptoms and demonstrated a favorable safety profile. The results suggest potential for zelicapavir as a first-in-class RSV treatment, reducing symptom duration and hospitalization rates in high-risk adults.