Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 646.00K | 486.00K | 1.06M | -227.00K | 1.11M | 1.09M |
Gross Profit | 477.00K | 486.00K | 1.06M | -227.00K | 1.11M | 1.09M |
EBITDA | -58.28M | -55.34M | -32.45M | -58.74M | -47.05M | -17.44M |
Net Income | -55.78M | -51.42M | -29.36M | -59.25M | -47.76M | -17.93M |
Balance Sheet | ||||||
Total Assets | 68.92M | 84.34M | 123.65M | 21.09M | 74.64M | 108.28M |
Cash, Cash Equivalents and Short-Term Investments | 63.18M | 80.48M | 119.17M | 16.64M | 68.14M | 103.11M |
Total Debt | 2.36M | 1.51M | 2.12M | 2.72M | 3.04M | 3.72M |
Total Liabilities | 12.16M | 13.95M | 9.37M | 9.01M | 9.93M | 16.30M |
Stockholders Equity | 56.77M | 70.39M | 114.29M | 12.08M | 64.72M | 91.98M |
Cash Flow | ||||||
Free Cash Flow | -50.12M | -42.29M | -25.87M | -49.93M | -45.46M | -12.35M |
Operating Cash Flow | -50.07M | -42.10M | -25.81M | -49.72M | -45.26M | -12.07M |
Investing Cash Flow | -8.47M | -13.15M | -61.00K | -740.30K | -200.40K | -275.40K |
Financing Cash Flow | 4.61M | 3.21M | 128.40M | -1.04M | 10.48M | 114.10M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
61 Neutral | $99.71M | ― | -46.28% | ― | -33.00% | 54.91% | |
43 Neutral | 100.48M | -0.81 | 0.00% | ― | 0.00% | -553.86% | |
42 Neutral | 18.89M | -0.66 | 88.41% | ― | -44.63% | 26.79% | |
38 Underperform | 67.18M | -6.74 | 0.00% | ― | -98.30% | 54.90% | |
35 Underperform | 37.87M | -0.39 | 0.00% | ― | 0.00% | -17.96% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On August 7, 2025, Vistagen reported its fiscal year 2026 first-quarter financial results and provided a corporate update. The company highlighted the progress of its lead program, fasedienol, for treating social anxiety disorder, with key trial results expected in late 2025 and early 2026. Vistagen is optimistic about the potential impact of fasedienol, as there is currently no FDA-approved acute treatment for social anxiety disorder. The company is also advancing other intranasal pherine product candidates for major depressive disorder and women’s health conditions. Financially, Vistagen reported increased R&D expenses due to its ongoing trials and a net loss of $15.1 million for the quarter ended June 30, 2025.
On June 25, 2025, Vistagen Therapeutics announced the appointment of Elissa Cote as Chief Corporate Development Officer, effective June 23, 2025. Ms. Cote, with nearly 30 years of experience in biopharmaceuticals, will lead strategic opportunities to advance Vistagen’s pherine platform and cultivate partnerships. Her appointment is seen as pivotal for Vistagen’s growth, as she brings expertise in business development and strategic transactions, which are crucial for the company’s future commercial launches and partnerships.
On June 17, 2025, Vistagen announced a prospectus supplement filed with the SEC to offer and sell shares of its common stock, aiming to raise up to $175 million. The company also reported its fiscal year 2025 financial results, highlighting significant progress in its clinical-stage pipeline, including the PALISADE program for fasedienol in social anxiety disorder. Vistagen’s ongoing trials and development efforts, such as the PALISADE-3 and PALISADE-4 trials, aim to address unmet needs in mental health and women’s health, with potential implications for future FDA submissions and market positioning.