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FDA Accepts Supplemental Biologics License Applications for BIMZELX® (bimekizumab-bkzx) for Moderate to Severe Hidradenitis Suppurativa and Additional

Application in moderate to severe hidradenitis suppurativa based on results from two Phase 3 studies where bimekizumab-bkzx showed clinically meaningful improvements vs. placebo at Week 16 which were sustained to Week 48Application for the additional bimekizumab-bkzx 2mL device presentations aims to provide more opt.

UCB : FDA Accepts Supplemental Biologics License Applications for BIMZELX (bimekizumab-bkzx) for Moderate to Severe Hidradenitis Suppurativa and Additional 2mL Device Presentations -April 04, 2024 at 01:04 am EDT

FDA Accepts Supplemental Biologics License Applications for BIMZELX® (bimekizumab-bkzx) for Moderate-to-Severe Hidradenitis Suppurativa and Additional 2mL Device Presentations

First Presentation of Year 4 BIMZELX® (bimekizumab-bkzx) Data Showed Long-Term Maintenance of Complete Skin Clearance in Moderate-to-Severe Plaque Psoriasis

First Presentation of Year 4 BIMZELX® (bimekizumab-bkzx) Data Showed Long-Term Maintenance of Complete Skin Clearance in Moderate-to-Severe Plaque Psoriasis
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First Presentation Of Year 4 BIMZELX® (Bimekizumab-Bkzx) Data Showed Long-Term Maintenance Of Complete Skin Clearance In Moderate-To-Severe Plaque Pso

First Presentation Of Year 4 BIMZELX® (Bimekizumab-Bkzx) Data Showed Long-Term Maintenance Of Complete Skin Clearance In Moderate-To-Severe Plaque Pso
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