Delivering extraordinary. Empowering ordinary.

We’re developing novel oral medicines for rare diseases to help patients take part in the everyday activities they enjoy.

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Structure-guided Drug Design

We combine traditional cell biology with medicinal chemistry to build synthetic compounds that bind to specific protein targets to fight disease.

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We are developing a pipeline of oral drugs for rare diseases, including our next generation kallikrein inhibitor for hereditary angioedema (HAE).

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Stay up to date with the latest discoveries, events, and reports from BioCryst.

July 3, 2019: BioCryst Reports Inducement Grants Under NASDAQ Listing Rule 5635(c)(4)
July 1, 2019: BioCryst Appoints Megan Sniecinski Chief Business Officer
June 27, 2019: Biocryst Begins Enrollment of Phase 1 Trial of BCX9930, an Oral Factor D Inhibitor for Complement-Mediated Diseases

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We are a collection of passionate individuals united by a commitment to scientific excellence and an unwavering focus on the needs of patients.

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