drugset / Trial / NCT03248531

A Study to Test the Efficacy, Safety and Pharmacokinetics of Bimekizumab in Subjects With Moderate to Severe Hidradenitis Suppurativa.

NCT03248531 ↗

Phase 2 Completed 90 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Hidradenitis suppurativa (HS) is a painful, long-term skin condition that causes abscesses and scarring on the skin.

Timeline

Start
2017-09-22
Primary completion
2018-11-23
Completion
2019-02-21

Outcome

Met primary endpoint

paper Bimekizumab demonstrated a higher HiSCR rate vs placebo at week 12 (57.3% vs 26.1%; posterior probability of superiority equaled 0.998, calculated using bayesian analysis). PMID 34406364 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody 40 mg —
Subject Bimekizumab Monoclonal antibody 320 mg —