| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 205.63M | 36.55M | 8.78M | 12.40M | 0.00 | 0.00 |
| Gross Profit | 204.64M | 36.55M | 8.78M | 12.40M | 0.00 | -1.93M |
| EBITDA | 33.10M | -99.19M | -112.30M | -102.81M | -85.09M | -50.32M |
| Net Income | 40.57M | -88.98M | -104.70M | -101.07M | -85.81M | -52.24M |
Balance Sheet | ||||||
| Total Assets | 360.26M | 271.56M | 228.34M | 256.07M | 238.87M | 297.93M |
| Cash, Cash Equivalents and Short-Term Investments | 248.31M | 216.90M | 201.39M | 229.59M | 219.81M | 287.31M |
| Total Debt | 2.91M | 2.32M | 2.06M | 2.36M | 1.51M | 1.07M |
| Total Liabilities | 52.16M | 42.53M | 68.78M | 71.22M | 21.09M | 11.85M |
| Stockholders Equity | 308.11M | 229.02M | 159.56M | 184.85M | 217.78M | 286.08M |
Cash Flow | ||||||
| Free Cash Flow | 52.37M | -87.05M | -82.68M | -35.83M | -68.11M | -43.27M |
| Operating Cash Flow | 52.85M | -86.85M | -81.07M | -31.87M | -66.91M | -42.22M |
| Investing Cash Flow | -124.93M | -107.47M | 105.95M | -45.88M | -76.43M | -1.05M |
| Financing Cash Flow | 5.62M | 131.09M | 53.01M | 46.41M | 1.28M | 108.11M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
65 Neutral | $1.68B | 44.64 | 15.02% | ― | 1128.17% | ― | |
56 Neutral | $1.28B | -10.00 | -23.41% | ― | ― | -37.07% | |
55 Neutral | $1.76B | -5.60 | -129.32% | ― | 597.19% | 0.45% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $1.89B | -26.51 | -28.07% | ― | ― | ― | |
46 Neutral | $1.23B | -71.95 | ― | ― | 42.05% | 76.50% |
On January 11, 2026, Stoke Therapeutics announced updated, accelerated timelines for its Phase 3 EMPEROR study of zorevunersen in Dravet syndrome, now expecting to complete enrollment of 150 patients in the second quarter of 2026 and to deliver a Phase 3 data readout in mid-2027 that is intended to support a rolling New Drug Application to the U.S. Food and Drug Administration starting in the first half of 2027. Following a recent multidisciplinary meeting held as part of zorevunersen’s Breakthrough Therapy Designation, the FDA requested additional information and made no immediate changes to the development program, but discussions continue around potential expedited pathways, while strong enrollment momentum, a global trial footprint, and a cash position of about $391.7 million as of December 31, 2025—together with collaboration proceeds from Biogen, expected to fund operations into 2028—underscore Stoke’s capacity to advance zorevunersen toward potential registration and commercialization in a field that currently lacks disease-modifying therapies for Dravet syndrome.
The most recent analyst rating on (STOK) stock is a Buy with a $39.00 price target. To see the full list of analyst forecasts on Stoke Therapeutics stock, see the STOK Stock Forecast page.
At the 2025 American Epilepsy Society Annual Meeting, Stoke Therapeutics and Biogen presented data supporting the potential of zorevunersen as a disease-modifying treatment for Dravet syndrome. Long-term studies demonstrated significant seizure reductions, cognitive and behavioral improvements, and enhanced quality of life for patients. The findings, including EEG analysis, suggest zorevunersen’s potential to address the underlying causes of Dravet syndrome, offering hope for improved patient outcomes.
The most recent analyst rating on (STOK) stock is a Buy with a $30.00 price target. To see the full list of analyst forecasts on Stoke Therapeutics stock, see the STOK Stock Forecast page.