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.

January 4, 2019: BioCryst Appoints Steve Aselage to Board of Directors
January 2, 2019: BioCryst Initiates Phase 1 Clinical Trial of Galidesivir
January 2, 2019: BioCryst to Present at 37th Annual J.P. Morgan Healthcare Conference

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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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