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BioCryst scraps internal drug discovery programs, leans on partnerships to cut costs

By Thomson Reuters Jun 29, 2026 | 7:21 AM

June 29 (Reuters) – BioCryst Pharmaceuticals said on Monday it would wind down its internal drug discovery programs and close its Alabama ​research facility by the end of 2026, ‌as it pivots to external partnerships to build its rare-disease pipeline and streamline expenses.

Shares of the drugmaker were down nearly 2% in premarket trading.

• The company said it ‌will ​leverage partnerships and its own ⁠commercial infrastructure to ⁠focus on identifying and advancing high-value rare-disease drug candidates.

• BioCryst lowered its 2026 adjusted operating expense forecast to $420 million to $440 million, compared with ​its prior view of $450 million to $470 million.

• The company reaffirmed its 2026 revenue forecast for ⁠Orladeyo at $625 million to $645 million. ⁠Total revenue projection stood at $635 million ​to $660 million.

• BioCryst markets Orladeyo, an oral treatment ​approved for hereditary angioedema, a rare disorder that ‌causes recurrent, unpredictable episodes of severe swelling.

• The company said it resolved a manufacturing delay for Orladeyo oral pellets for children aged 2 to ⁠under 12 years, and expects the product to be available in early August.

• BioCryst said it will focus ⁠on two ‌experimental drugs nearing commercialization: navenibart for ⁠HAE and BCX17725 for Netherton syndrome, ​a ‌rare skin disease.

• The company said ​top-line data ⁠from a late-stage study of navenibart are expected in Q3 2027, while proof-of-concept data for BCX17725 in Netherton syndrome are expected by the end of 2026.

(Reporting by Kunal Das in Bengaluru; Editing by ​Shreya Biswas)