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You are here: Industry Insights > Vonvendi

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U.S. Food and Drug Administration Accepts Takeda’s Supplemental Biologics License Application for Adult Prophylactic Use of VONVENDI [von Willebrand factor (Recombinant)] firstwordpharma
June 15, 2021
Takeda Pharmaceutical Company Limited announced today that FDA has accepted for review the sBLA) for VONVENDI® [von Willebrand factor (Recombinant)] for prophylactic treatment to prevent or reduce the frequency of bleeding episodes in adults.

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