| Breakdown | Dec 2025 | Mar 2025 | Mar 2024 | Mar 2023 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| EBITDA | -29.70M | -26.69M | -45.03M | -25.51M | -14.50M |
| Net Income | -28.85B | -24.59M | -56.20M | -25.33M | -14.49M |
Balance Sheet | |||||
| Total Assets | 21.08B | 13.93M | 10.21M | 36.02M | 46.00M |
| Cash, Cash Equivalents and Short-Term Investments | 19.53B | 10.55M | 5.75M | 28.38M | 45.69M |
| Total Debt | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Total Liabilities | 4.23B | 4.62M | 17.96M | 7.70M | 1.51M |
| Stockholders Equity | 16.85B | 9.31M | -7.75M | 28.32M | 44.49M |
Cash Flow | |||||
| Free Cash Flow | -25.62B | -21.89B | -39.97M | -17.31M | -9.13M |
| Operating Cash Flow | -25.62B | -21.89B | -39.97M | -17.31M | -9.13M |
| Investing Cash Flow | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Financing Cash Flow | 34.60B | 26.69B | 17.34M | 4.61K | 46.74M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
58 Neutral | $184.54M | -7.27 | -10.35% | ― | -42.62% | ― | |
54 Neutral | $198.08M | -0.98 | -97.41% | ― | ― | -60.99% | |
53 Neutral | $140.20M | -1.17 | -95.12% | ― | -99.07% | -10347.56% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $66.79M | >-0.01 | -0.68% | ― | ― | 62.84% | |
45 Neutral | $94.79M | -11.27 | -62.18% | ― | -58.26% | -53.20% |
On February 12, 2026, Annovis Bio said an independent Data and Safety Monitoring Board issued a positive safety recommendation at six months for its pivotal Phase 3 Alzheimer’s trial of buntanetap, allowing the U.S. study to continue without modification. The board found no safety concerns and reported that six-month safety data in Alzheimer’s patients were consistent with those previously seen in Parkinson’s patients, with further safety reviews scheduled at 12 and 18 months.
Management noted that alignment of safety outcomes across the Alzheimer’s and Parkinson’s programs has led regulators to indicate they may consider combined safety data in a future new drug application, potentially streamlining buntanetap’s path to market. The Phase 3 Alzheimer’s trial is currently recruiting and reported to be 40% complete, with the first symptomatic efficacy readout expected in early 2027 and a disease-modifying readout anticipated in early 2028, underscoring a long development runway for investors and patients.
The most recent analyst rating on (ANVS) stock is a Hold with a $2.50 price target. To see the full list of analyst forecasts on Annovis Bio stock, see the ANVS Stock Forecast page.
On January 28, 2026, Annovis Bio, Inc. held a webinar, supported by a prepared presentation that was made available to participants and stakeholders. The event signaled an effort by the company to formally communicate information to the market via a structured public forum, though no additional operational or strategic details were disclosed in the announcement.
The most recent analyst rating on (ANVS) stock is a Hold with a $3.00 price target. To see the full list of analyst forecasts on Annovis Bio stock, see the ANVS Stock Forecast page.