drugset / Trial / NCT02203851

Extension Trial Assessing the Safety and Efficacy of BI 655066/ABBV-066/Risankizumab in Patients With Moderate to Severe Chronic Plaque Psoriasis

NCT02203851

Phase 2 Completed 110 enrolled AbbVie Boehringer Ingelheim · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of Study M16-009 was to investigate the safety of risankizumab in participants with moderate to severe chronic plaque psoriasis who were receiving long-term treatment. Additional study objectives were to further investigate the long-term efficacy, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of risankizumab.

Timeline

Start
2014-11-20
Primary completion
2018-09-04
Completion
2018-09-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody 90 mg Subcutaneous
Subject Risankizumab Monoclonal antibody 180 mg Subcutaneous

Indications