Grifols Receives FDA Approval for Fesilty, Plans US Launch in 2026

viernes, 19 de diciembre de 2025, 11:26 am ET1 min de lectura
GRFS--

Grifols, a parent company of Biotest AG, has received FDA approval for Fesilty, a human fibrinogen product for treating acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency. The company plans to launch the product in the US in the first half of 2026.

Grifols Receives FDA Approval for Fesilty, Plans US Launch in 2026

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