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

Outcome

Met primary endpoint

paper The primary and all hierarchical secondary endpoints were met at week 16. PMID 36495881 ↗

registry analysis (superiority test); Placebo vs Bimekizumab 160mg; p <0.001; Odds Ratio (OR) 11.139 (95% CI 5.402 to 22.969); Regression, Logistic NCT03896581 ↗

release “BE COMPLETE met its primary endpoint, demonstrating that significantly more patients treated with bimekizumab achieved 50 percent or greater improvement” ucb.com ↗

release “Both studies met their primary endpoint of ACR50 at week 16” ucb.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 160 mg Subcutaneous

Indications