drugset / Trial / NCT03928704

A Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Nonradiographic Axial Spondyloarthritis

NCT03928704 ↗

Phase 3 Completed 274 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 nonradiographic axial spondyloarthritis (nr-axSpA).

Timeline

Start
2019-04-25
Primary completion
2022-06-29
Completion
2023-04-17

Outcome

Met primary endpoint

paper primary (ASAS40, nr-axSpA: 47.7% bimekizumab vs 21.4% placebo; r-axSpA: 44.8% vs 22.5%; p<0.001) PMID 36649967 ↗

release “The BE MOBILE 1 study met the primary and all ranked secondary endpoints” 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

Indications