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

Drugs

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

Indications