drugset / Trial / NCT02905006

Study to Evaluate Safety and Efficacy of Different Doses of Bimekizumab in Patients With Chronic Plaque Psoriasis

NCT02905006 ↗

Phase 2 Completed 250 enrolled UCB Biopharma S.P.R.L. Parexel · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2b, multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose ranging study to investigate the safety, efficacy, pharmacokinetics (PK), and pharmacodynamics (PD) of Bimekizumab compared with placebo in adult subjects with moderate to severe chronic plaque psoriasis in order to guide the selection of doses and clinical indices in the Phase 3 development program.

Timeline

Start
2016-08
Primary completion
2017-06
Completion
2017-07

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo (FAS) vs Bimekizumab 64 mg Q4W (FAS); p <0.0001; Regression, Logistic; NCT02905006 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody — —

Indications