drugset / Trial / NCT04242498

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa

NCT04242498

Phase 3 Completed 509 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the efficacy and safety of bimekizumab in study participants with moderate to severe hidradenitis suppurativa (HS)

Timeline

Start
2020-03-02
Primary completion
2021-11-09
Completion
2022-09-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 320 mg Subcutaneous