drugset / Trial / NCT02684357

BI 655066 Versus Placebo & Active Comparator (Ustekinumab) in Patients With Moderate to Severe Chronic Plaque Psoriasis

NCT02684357

Phase 3 Completed 577 enrolled AbbVie Boehringer Ingelheim · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a randomized double blind, double dummy, placebo and active comparator controlled, parallel design study that is being performed to assess the safety and efficacy of risankizumab (BI 655066) to support registration for the treatment of moderate to severe chronic plaque psoriasis in adult patients.

Timeline

Start
2016-03
Primary completion
2016-12
Completion
2017-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody 150 mg Subcutaneous
Comparator Ustekinumab Monoclonal antibody 45 mg Subcutaneous
Comparator Ustekinumab Monoclonal antibody 90 mg Subcutaneous

Indications