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Kerecis to Provide Multiple Updates on its Medical-Fish-Skin Technology at the European Wound Management Association Meeting

Kerecis to Provide Multiple Updates on its Medical-Fish-Skin Technology at the European Wound Management Association Meeting
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FDA Accepts Supplemental Biologics License Applications for BIMZELX® (bimekizumab-bkzx) for Moderate-to-Severe Hidradenitis Suppurativa and Additional 2mL Device Presentations

/PRNewswire/ UCB, a global biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the.

Bruxelles capitaleErica puntelAntje witteHidradenitis suppurativaEmmanuel caeymaexGroup of companiesDrug administrationUcb incImmunology solutionsUs communicationsBiologics license applicationExecutive vice presidentImportant safety informationUnited statesHerpes simplex infectionsEuronext brussels

FDA Accepts sBLA for Bimekizumab-bkzx in Hidradenitis Suppurativa Treatment

Bimekizumab-bkzx (Bimzelx; Union Chimique Belge) is a humanized monoclonal immunoglobulin G1 antibody that inhibits interleukin (IL)-17A and IL-17F.

Study participants with moderateSevere hidradenitis suppurativa

FDA Accepts sBLA For Bimekizumab-Bkzx in 3 New Spondyloarthritides Indications

The 3 bimekizumab indications include psoriatic arthritis, non-radiographic axial spondyloarthritis, and ankylosing spondylitis.

Emmanuel caeymaexHidradenitis suppurativaUnion chimique belgeImmunology solutionsInternational hidradenitis suppurativa severity score systemStudy participants with moderateSevere hidradenitis suppurativaEuropean hidradenitis suppurativa

Lutikizumab Showed Positive Results in a Phase 2 Trial of Adults with Moderate to Severe Hidradenitis Suppurativa as Program Advances to Phase 3

Phase 2 data in adults with hidradenitis suppurativa (HS) who had previously failed anti-TNF therapy who received lutikizumab (ABT-981) 300 mg weekly or 300 mg every other week showed higher response rates in HiSCR 50 at week 16 than those treated.

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