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UCB announces FDA accepts sBLA for BIMZELX

UCB announces FDA accepts sBLA for BIMZELX

UCB announced that the U.S. FDA has accepted for review the supplemental Biologics License Application for BIMZELX, an IL-17A and IL-17F inhibitor, for the treatment of adults with moderate-to-severe hidradenitis suppurativa. In addition, a second sBLA for the BIMZELX 2mL device presentations has also been accepted.

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