FDA Expands Indication for Hemlibra to Include Non-Factor VIII Inhibitors
Prophylactic treatment reduced bleed rates in adults and children
By Nikki Kean
The FDA has expanded the indication for emicizumab-kxwh injection (Hemlibra, Genentech) to include adults and children with hemophilia A without factor VIII (FVIII) inhibitors. Hemlibra was first approved in 2017 for patients with hemophilia A with FVIII inhibitors.
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