Denali Therapeutics Surges on FDA Approval of Tividenofusp Alfa for Rare Genetic Disease Hunter Syndrome

miércoles, 25 de marzo de 2026, 9:15 am ET1 min de lectura
DNLI--

Denali Therapeutics (DNLI) gained 9% in premarket trading after the FDA approved its lead asset, tividenofusp alfa, for the treatment of Hunter syndrome, a rare genetic disease.

Denali Therapeutics Surges on FDA Approval of Tividenofusp Alfa for Rare Genetic Disease Hunter Syndrome

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