| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 599.82M | 450.71M | 331.41M | 270.83M | 157.17M | 17.81M |
| Gross Profit | 583.80M | 438.23M | 326.75M | 264.23M | 149.91M | 16.14M |
| EBITDA | 83.87M | 12.81M | -116.33M | -143.85M | -121.74M | -167.56M |
| Net Income | -8.78M | -88.88M | -226.54M | -247.12M | -184.06M | -182.81M |
Balance Sheet | ||||||
| Total Assets | 446.42M | 490.42M | 516.96M | 550.00M | 588.15M | 334.71M |
| Cash, Cash Equivalents and Short-Term Investments | 212.87M | 321.06M | 388.99M | 424.31M | 507.60M | 300.37M |
| Total Debt | 683.11M | 841.42M | 825.15M | 741.45M | 593.24M | 279.50M |
| Total Liabilities | 834.31M | 966.35M | 972.49M | 844.60M | 695.14M | 353.98M |
| Stockholders Equity | -387.89M | -475.93M | -455.53M | -294.60M | -106.99M | -19.26M |
Cash Flow | ||||||
| Free Cash Flow | 47.34M | -53.14M | -97.31M | -163.20M | -144.54M | -137.73M |
| Operating Cash Flow | 49.68M | -52.02M | -95.14M | -161.85M | -142.16M | -137.22M |
| Investing Cash Flow | 87.59M | 52.59M | -131.50M | -128.24M | 15.80M | -6.86M |
| Financing Cash Flow | -135.48M | -5.76M | 32.48M | 88.03M | 359.67M | 302.70M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
79 Outperform | $2.09B | 28.14 | 20.65% | ― | 20.62% | ― | |
71 Outperform | $1.80B | 151.16 | 4.52% | ― | 14.05% | 241.86% | |
60 Neutral | $6.92B | -18.70 | -68.70% | ― | -100.00% | 53.89% | |
55 Neutral | $1.57B | ― | ― | ― | 45.38% | 92.85% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $2.34B | -7.31 | -21.37% | ― | 47.15% | -311.26% | |
41 Neutral | $1.77B | -7.62 | -32.44% | ― | -73.94% | -31.70% |
On December 12, 2025, BioCryst Pharmaceuticals announced the FDA approval of its new drug application for an oral pellet formulation of ORLADEYO® (berotralstat) for prophylactic therapy in pediatric patients with hereditary angioedema (HAE) aged 2 to less than 12 years. This approval marks a significant milestone as it introduces the first and only oral prophylactic treatment for this age group, offering a more convenient administration method compared to previous intravenous or subcutaneous options. The approval was supported by positive interim data from the APeX-P clinical trial, which demonstrated early and sustained reductions in monthly attack rates. The new formulation aims to alleviate the treatment burden for young patients and their caregivers, potentially transforming the management of HAE in children.
On December 9, 2025, Nancy J. Hutson, Ph.D. announced her intention to retire from BioCryst Pharmaceuticals’ Board of Directors, effective by the earlier of the company’s 2026 annual meeting or the closing of its proposed acquisition of Astria Therapeutics. Dr. Hutson, who has served as Chair of the Board and various committees, cited no disagreements with the company. In response, the Board elected Vincent J. Milano as the next Chair, effective upon her retirement.
On December 3, 2025, BioCryst Pharmaceuticals announced the early termination of the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act for its proposed acquisition of Astria Therapeutics. This development satisfies one of the conditions for the merger, which is expected to close in the first quarter of 2026, pending other customary closing conditions. The merger is anticipated to enhance BioCryst’s market position, although it carries risks such as potential integration challenges and financial implications.
In the third quarter of 2025, BioCryst Pharmaceuticals reported significant financial growth, with ORLADEYO net revenue reaching $159.1 million, a 37% increase year-over-year. The company completed the sale of its European ORLADEYO business, using proceeds to retire Pharmakon term debt, and announced a definitive agreement to acquire Astria Therapeutics, expected to close in the first quarter of 2026. These strategic moves are expected to enhance BioCryst’s market position and financial stability, with the company raising its full-year revenue guidance and lowering its operating expense outlook for 2025.
On October 14, 2025, BioCryst Pharmaceuticals announced a merger agreement with Astria Therapeutics, which will see Astria become a wholly owned subsidiary of BioCryst. The merger, expected to close in the first quarter of 2026, involves an exchange of shares and cash, with Astria’s stock to be delisted from Nasdaq. The merger aims to enhance BioCryst’s market position and operational capabilities, with financing commitments secured from Blackstone to support the transaction. The merger agreement includes various conditions and provisions, such as stockholder approval and regulatory clearances, with potential termination fees if the agreement is not fulfilled.
On October 1, 2025, BioCryst Pharmaceuticals completed the sale of its European ORLADEYO business to Neopharmed Gentili for $250 million, with potential future milestones of up to $14 million. This transaction allows BioCryst to focus on its U.S. operations, improve its operating margin, and retire a significant portion of its debt, positioning the company for future strategic activities. Neopharmed Gentili will handle the commercialization of ORLADEYO in Europe, ensuring continuity for the brand and patients.