drugset / Trial / NCT02969525

A Study to Evaluate the Dose Response Based on the Efficacy, Safety and Tolerability of Bimekizumab in Subjects With Active Psoriatic Arthritis Which is a Type of Inflammatory Arthritis

NCT02969525 ↗

Phase 2 Completed 206 enrolled UCB Biopharma S.P.R.L.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a study to evaluate the dose response based on the efficacy, safety and tolerability of bimekizumab in subjects with active psoriatic arthritis.

Timeline

Start
2016-10
Primary completion
2017-11
Completion
2018-07

Outcome

Met primary endpoint

registry analysis (other test); Placebo (FAS) vs BKZ 160 mg (FAS); p =0.001; Odds Ratio (OR) 8.1 (95% CI 2.28 to 28.74); NCT02969525 ↗

Drugs

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

Indications