drugset / Trial / NCT02963506

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

NCT02963506 ↗

Phase 2 Completed 303 enrolled UCB Biopharma S.P.R.L.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a study to evaluate the efficacy and safety of different doses of bimekizumab in subjects with active Ankylosing Spondylitis (AS).

Timeline

Start
2016-10
Primary completion
2017-10
Completion
2018-08

Outcome

Met primary endpoint

paper At week 12, significantly more bimekizumab-treated patients achieved ASAS40 vs placebo (NRI: 29.5%-46.7% vs 13.3%; p<0.05 all comparisons; PMID 32253184 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 16 mg Subcutaneous
Subject Bimekizumab Monoclonal antibody 64 mg Subcutaneous
Subject Bimekizumab Monoclonal antibody 160 mg Subcutaneous
Subject Bimekizumab Monoclonal antibody 320 mg Subcutaneous