Biohaven Reports Recent Business Developments and Third Quarter 2026 Financial Results
Biohaven said the FDA accepted its resubmitted new drug application for Vyglxia (troriluzole) in spinocerebellar ataxia, with a user fee goal date in the first quarter of 2027. The company also announced an exclusive global license with SK Biopharmaceuticals.
Why it matters — The update covers a regulatory milestone for Vyglxia and a newly announced licensing agreement relevant to Biohaven's business.