| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 14.97M | 802.00K | 44.70M | 268.00K | 4.82M |
| Gross Profit | 0.00 | 14.97M | 802.00K | 44.70M | 268.00K | -9.57M |
| EBITDA | -69.35M | -55.37M | -71.06M | 5.19M | -47.87M | -16.56M |
| Net Income | -75.88M | -61.07M | -73.35M | 5.34M | -50.87M | -17.71M |
Balance Sheet | ||||||
| Total Assets | 109.20M | 160.33M | 214.51M | 270.20M | 280.71M | 50.67M |
| Cash, Cash Equivalents and Short-Term Investments | 74.27M | 110.66M | 142.09M | 194.38M | 214.05M | 43.27M |
| Total Debt | 11.57M | 12.01M | 12.98M | 8.77M | 7.22M | 46.36M |
| Total Liabilities | 24.64M | 30.19M | 27.51M | 27.00M | 28.15M | 53.81M |
| Stockholders Equity | 84.47M | 130.03M | 186.78M | 242.90M | 252.13M | -3.54M |
Cash Flow | ||||||
| Free Cash Flow | -30.97M | -29.83M | -56.34M | -20.57M | -33.73M | -11.32M |
| Operating Cash Flow | -30.65M | -28.94M | -50.92M | -14.43M | -32.58M | -11.03M |
| Investing Cash Flow | 136.00K | -892.00K | -5.41M | -5.75M | -12.91M | -293.00K |
| Financing Cash Flow | 839.00K | 2.16M | 1.87M | 325.00K | 222.74M | 41.44M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
41 Neutral | $30.17M | ― | -62.30% | ― | -100.00% | -26.30% | |
41 Neutral | $16.54M | -5.87 | -42.29% | ― | ― | -21.99% | |
40 Underperform | $27.31M | -0.44 | -44.88% | ― | ― | -0.50% | |
40 Underperform | $65.72M | -0.54 | -141.82% | ― | -55.88% | 6.14% | |
39 Underperform | $78.62M | -0.72 | -118.95% | ― | ― | 31.98% | |
38 Underperform | $19.33M | -1.49 | -92.74% | ― | 280.77% | 32.82% |
On December 10, 2025, Barinthus Biotherapeutics announced an update on its Phase 1 AVALON clinical trial for VTP-1000, an antigen-specific immunotherapy for celiac disease. The single ascending dose portion of the trial showed that VTP-1000 was well-tolerated with no serious adverse events and demonstrated a dose-dependent pharmacological effect. The ongoing multiple ascending dose portion, which includes a gluten challenge, is expected to provide further insights in the second half of 2026. This development marks a significant step in addressing the unmet needs in celiac disease treatment, potentially positioning Barinthus Bio as a leader in immune tolerance therapies.
On September 29, 2025, Barinthus Biotherapeutics and Clywedog Therapeutics entered into a merger agreement to form a combined entity named Clywedog Therapeutics, Inc. The merger, expected to close in the first half of 2026, will create a company with a diversified pipeline targeting metabolic and autoimmune diseases, including Type 1 and Type 2 diabetes and celiac disease. The transaction will result in Clywedog stockholders owning approximately 66% and Barinthus shareholders owning about 34% of the new company. The combined company will be supported by existing cash and additional investments from OrbiMed and Torrey Pines Investment LLC, and is expected to trade on NASDAQ under the symbol ‘CLYD’.