drugset / Trial / NCT02786732

Study to Evaluate Broadlumab vs Placebo and Ustekinumab

NCT02786732

Phase 3 Terminated 15 enrolled MedDerm Associates
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the efficacy and safety of Induction and Maintenance Regimens of Brodalumab compared with Placebo and Ustekinumab in subjects with moderate to severe plaque psoriasis.

Timeline

Start
2012-08
Primary completion
2017-06
Completion
2017-10

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