drugset / Trial / NCT03896581

A Study to Evaluate the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis

NCT03896581

Phase 3 Completed 400 enrolled UCB Biopharma SRL
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of tumor necrosis factor alpha-inadequate responders (TNFα-IR) subjects with active Psoriatic Arthritis (PsA).

Timeline

Start
2019-03-28
Primary completion
2021-12-08
Completion
2022-02-14

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 160 mg Subcutaneous

Indications