| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 6.61M | 566.00K | 392.00K | 1.50M | 208.38M | 12.62M |
| Gross Profit | 6.59M | 566.00K | 392.00K | 1.50M | 208.38M | 12.62M |
| EBITDA | -40.29M | -57.77M | -57.01M | -54.17M | 124.45M | -81.12M |
| Net Income | -36.33M | -26.43M | -52.34M | -54.17M | 122.83M | -81.04M |
Balance Sheet | ||||||
| Total Assets | 63.85M | 92.17M | 144.03M | 155.27M | 194.54M | 75.93M |
| Cash, Cash Equivalents and Short-Term Investments | 25.60M | 53.08M | 105.83M | 129.00M | 187.80M | 72.03M |
| Total Debt | 13.76M | 14.76M | 16.00M | 16.54M | 0.00 | 0.00 |
| Total Liabilities | 19.15M | 23.94M | 56.23M | 22.99M | 14.80M | 32.29M |
| Stockholders Equity | 44.70M | 68.23M | 87.80M | 132.27M | 179.75M | 43.63M |
Cash Flow | ||||||
| Free Cash Flow | -37.96M | -56.03M | -45.92M | -56.65M | 118.43M | -51.97M |
| Operating Cash Flow | -37.93M | -55.96M | -45.78M | -55.23M | 118.61M | -51.58M |
| Investing Cash Flow | 43.50M | 54.59M | -2.58M | -87.88M | -1.82M | 34.65M |
| Financing Cash Flow | 28.00K | 622.00K | 30.54M | 180.66K | 904.08K | 47.07M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
52 Neutral | $104.68M | -2.88 | -60.06% | ― | 946.61% | -11.30% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
46 Neutral | $101.15M | -0.67 | -49.18% | ― | -33.76% | 17.54% | |
46 Neutral | $208.58M | -3.02 | -131.71% | ― | -100.00% | 79.01% | |
44 Neutral | $137.93M | -1.16 | -338.75% | ― | 74.60% | -58.14% | |
43 Neutral | $186.51M | -1.00 | ― | ― | -63.96% | -28.50% | |
35 Underperform | $98.99M | -0.59 | -209.00% | ― | ― | 40.22% |
On December 18, 2025, Ovid Therapeutics reported Phase 1 results for OV350, the first known direct activator of the potassium-chloride cotransporter 2 (KCC2) to be dosed in humans, showing a favorable safety and tolerability profile with no treatment-related serious adverse events, predictable pharmacokinetics, and exploratory qEEG data consistent with central KCC2 modulation. The intravenous “tool” program achieved pharmacologically active exposure levels and provided key human safety and mechanistic data that underpin Ovid’s decision to halt further IV development of OV350 while accelerating its more potent, oral KCC2 activators, particularly OV4071, which is slated to enter Phase 1/1b testing in 2026 for psychosis associated with Parkinson’s disease and Lewy body dementia and potentially other neuropsychiatric conditions, bolstering the company’s positioning in first-in-class therapies targeting neural hyperexcitability.
On December 11, 2025, Ovid Therapeutics held a special meeting where stockholders approved three key proposals. The first proposal increased the authorized shares of common stock from 125 million to 315 million. The second proposal allowed the conversion of Series B Preferred Stock and the exercise of Series A and B Warrants, while the third approved the issuance of securities to CEO Jeremy Levin. These approvals are significant for the company’s capital structure and compliance with Nasdaq rules.
On October 2, 2025, Ovid Therapeutics entered into a Securities Purchase Agreement to issue and sell Series B convertible preferred stock and warrants in a private placement, potentially raising up to $175.1 million. The proceeds will be used for research and development, corporate expenses, and working capital. Additionally, Ovid announced positive results from a Phase 1 study of OV329, a GABA-aminotransferase inhibitor for drug-resistant epilepsies, showing strong inhibitory activity and a favorable safety profile, with plans to advance to Phase 2a trials.