drugset / Trial / NCT03928743

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Ankylosing Spondylitis

NCT03928743 ↗

Phase 3 Completed 332 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to demonstrate the efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared to placebo in the treatment of subjects with active ankylosing spondylitis (AS).

Timeline

Start
2019-04-25
Primary completion
2021-09-03
Completion
2022-08-08

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo (up to Week 16) vs Bimekizumab 160 mg Q4W (up to Week 16); p <0.001; Odds Ratio (OR) 2.88 (95% CI 1.71 to 4.87); Regression, Logistic NCT03928743 ↗

release “The BE MOBILE 2 study met its primary endpoint” ucb.com ↗

release “The two phase 3 studies, BE MOBILE 1 and BE MOBILE 2, met all primary and ranked secondary endpoints at Week 16.” ucb.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 160 mg Subcutaneous