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BioCryst Pharmaceuticals Inc

BioCryst Pharmaceuticals, Inc., a biotechnology company, developing and commercializing medicines for hereditary angioedema (HAE) and other rare diseases. The company markets peramivir injection, an intravenous neuraminidase inhibitor for the treatment of acute uncomplicated and seasonal influenza under the RAPIVAB, RAPIACTA, and PERAMIFLU names; and ORLADEYO, an oral serine protease inhibitor to treat HAE. It is also developing BCX17725, a protein therapeutic for netherton syndrome which is in phase 1; Avoralstat, an ocular plasma kallikrein inhibitor for diabetic macular edema that is in Phase 1; Navenibart, a monoclonal antibody plasma kallikrein inhibitor for HAE which is in Phase 3; BCX17725, an investigational protein therapeutic KLK5 inhibitor for the treatment of netherton syndrome that is in phase 1 clinical trial; STAR-0310, a monoclonal antibody OX40 antagonist for the treatment of atopic dermatitis which is in Phase 1a trial. The company has collaborations and in-license relationships with the Torii Pharmaceutical Co., Ltd., Shionogi & Co., Ltd., and Green Cross Corporation; National Institute of Allergy and Infectious Diseases; Biomedical Advanced Research and Development Authority; the U.S. Department of Health and Human Services; and Albert Einstein College of Medicine of Yeshiva University and Industrial Research, Ltd. BioCryst Pharmaceuticals, Inc. was founded in 1986 and is headquartered in Durham, North Carolina.

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Biotech & Genomic Medicine

BioCryst Q2 2026 Earnings Call Transcript

BioCryst Pharmaceuticals reported second quarter 2026 results, with ORLADEYO revenue of $158.2 million, up 10% year-over-year on a comparable basis, and total revenue up 45% year-over-year excluding the European divestiture. The company completed enrollment of its pivotal ALPHA-ORBIT trial for navenibart ahead of schedule, with top-line data expected in the third quarter of 2027. BioCryst also announced it has discontinued internal discovery programs and will close its Birmingham research facility by year-end, shifting to an external innovation model, and raised its full-year total revenue guidance to $690 million to $715 million while maintaining ORLADEYO revenue guidance of $625 million to $645 million. The company ended the quarter with just over $350 million in cash, cash equivalents, and investments, and posted a non-GAAP operating profit of $113.2 million.
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Biotech & Genomic Medicine

BioCryst's First Profitable Year Fuels Takeover Speculation, Takeda Tops Buyer List

BioCryst Pharmaceuticals achieved its first full year of profitability in 2025, with second-quarter 2026 revenue rising 34 percent to 218 million dollars, intensifying acquisition speculation. Takeda ranks as the most plausible acquirer because its HAE injectable Takhzyro is directly threatened by BioCryst's pipeline asset navenibart, while AstraZeneca places second through its Alexion rare-disease platform. The company's oral HAE drug Orladeyo generated 158.2 million dollars in quarterly revenue and carries full-year guidance of 625 million to 645 million dollars, and navenibart's pivotal trial data is expected in the third quarter of 2027. BioCryst closed at 9.84 dollars on August 10, 2026, giving it a market capitalization of roughly 2.5 billion dollars, and analysts hold a consensus price target of 20.82 dollars. No deal talks have been confirmed, and private equity interest is seen as secondary to strategic buyers.
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BCRX2

BioCryst raises 2026 total revenue guidance to $690 million to $715 million

BioCryst Pharmaceuticals raised its full-year 2026 total revenue guidance to a range of $690 million to $715 million, driven by the closing of a navenibart European license agreement. The company maintained its ORLADEYO revenue guidance of $625 million to $645 million and reduced its non-GAAP operating cost guidance to $420 million to $440 million from a prior range of $450 million to $470 million. Second-quarter ORLADEYO revenue reached $158.2 million, contributing to a non-GAAP operating profit of $113.2 million. The company also began shipping ORLADEYO oral pellets for pediatric patients and reported 47 prescriptions through July 31, ahead of full-year expectations. BioCryst ended the quarter with over $350 million in cash, cash equivalents, and investments, and generated positive cash flow even excluding upfront proceeds from the license agreement.
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Biotech & Genomic Medicine

BioCryst Stock Appears Undervalued Despite 54.7% Three-Year Return

BioCryst Pharmaceuticals stock has returned 54.7% over three years yet still screens as undervalued on valuation metrics. The company trades at a price-to-sales ratio of about 3.2 times, well below the biotech industry average of roughly 12.4 times and a peer group average near 12.1 times. Simply Wall St's fair P/S ratio for BioCryst is about 4.9 times, suggesting the market is pricing in cautious expectations. The shift toward external innovation and partnerships supports a focused rare disease pipeline, but closing the Birmingham facility and ending internal discovery programs add execution risk. The key debate is whether the discount reflects genuine mispricing or a fair response to risks around its concentrated pipeline.
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Biotech & Genomic Medicine2

BioCryst Pharmaceuticals Ends Internal Discovery, Closes Birmingham Facility

BioCryst Pharmaceuticals is ending its internal discovery programs and closing its Birmingham, Alabama facility. The company plans to pivot toward external innovation in rare diseases, focusing on partnered or acquired assets. This corporate shift follows renewed M&A discussion in biotech after a large sector acquisition. The decision reshapes how future drug candidates may enter the pipeline, with a heavier tilt toward collaborations and in-licensing. For investors, the change raises questions around future deal activity, research productivity, and capital allocation.
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