drugset / Trial / NCT06624228

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Study Participants With Active Psoriatic Arthritis

NCT06624228

Phase 3 Completed 684 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to compare the efficacy of bimekizumab versus risankizumab after 16 weeks of treatment in study participants with active psoriatic arthritis (PsA).

Timeline

Start
2024-10-21
Primary completion
2026-02-06
Completion
2026-06-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody
Comparator Risankizumab Monoclonal antibody

Indications