drugset / Trial / NCT01708629

Efficacy and Safety of Brodalumab Compared With Placebo and Ustekinumab in Moderate to Severe Plaque Psoriasis Subjects

NCT01708629

Phase 3 Terminated 1881 enrolled Bausch Health Americas, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of brodalumab at two different doses compared with placebo in participants with moderate to severe plaque psoriasis. A second purpose of this study is to assess the safety and efficacy brodalumab at two different doses compared with ustekinumab in participants with moderate to severe plaque psoriasis. A third purpose of this study is to assess the safety and efficacy of 4 maintenance regimens of brodalumab.

Timeline

Start
2012-09
Primary completion
2014-08
Completion
2015-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Brodalumab Monoclonal antibody 140 mg Subcutaneous
Subject Brodalumab Monoclonal antibody 210 mg Subcutaneous
Comparator Ustekinumab Monoclonal antibody 45 mg Subcutaneous
Comparator Ustekinumab Monoclonal antibody 90 mg Subcutaneous

Indications