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

Outcome

Met primary endpoint

paper At week 16, significantly more patients receiving bimekizumab (189 [44%] of 431) reached ACR50 response versus placebo PMID 36493791 ↗

registry Placebo vs BKZ 160 mg Q4W; p <0.001; Odds Ratio (OR) 7.082 (95% CI 4.583 to 10.943) NCT03895203 ↗

release “The BE OPTIMAL study met the primary endpoint and all ranked secondary endpoints with statistical significance” ucb.com ↗

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

Publications

Drugs

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

Indications