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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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