FDA approves expanded indication for Vonvendi

8 September 2025

The US Food and Drug Administration (FDA) has approved the supplemental Biologics License Application (sBLA) for Vonvendi [von Willebrand factor (Recombinant)].

Developed by Japanese pharma major Takeda (TYO: 4502), the drug’s use is now expanded to include routine prophylaxis to reduce the frequency of bleeding episodes in adults with von Willebrand Disease (VWD), including those with Type 1 and 2 disease, and on-demand and perioperative management of bleeding in pediatric patients with VWD.

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