Application in moderate-to-severe hidradenitis suppurativa based on results from two Phase 3 studies where BIMZELX® (bimekizumab-bkzx) showed clinically meaningful improvements vs. placebo at Week 16 which were sustained to Week 48 Application for the additional BIMZELX 2mL device…
FDA Accepts Supplemental Biologics License Applications for BIMZELX® (bimekizumab-bkzx) for Moderate-to-Severe Hidradenitis Suppurativa and Additional 2mL Device Presentations
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