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.

April 1, 2019: BioCryst to Present at Upcoming Investor Conferences
March 4, 2019: BioCryst Reports Fourth Quarter and Full Year 2018 Financial Results
March 4, 2019: BioCryst Advancing BCX9930, an Oral Factor D Inhibitor for Complement-Mediated Diseases, into Phase 1 Development

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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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