drugset / Trial / NCT03895203

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

NCT03895203

Phase 3 Completed 852 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 subjects with active Psoriatic Arthritis (PsA).

Timeline

Start
2019-04-03
Primary completion
2021-08-17
Completion
2022-07-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject Bimekizumab Monoclonal antibody 160 mg Subcutaneous

Indications