drugset / Trial / NCT03926169

A Global Study Comparing Risankizumab to Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa

NCT03926169

Phase 2 Completed 243 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to assess the safety and efficacy of risankizumab 180 mg and 360 mg versus placebo for the treatment of signs and symptoms of moderate to severe hidradenitis suppurativa (HS) in adult participants diagnosed for at least one year before the Baseline visit.

Timeline

Start
2019-06-03
Primary completion
2021-02-02
Completion
2021-08-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody 180 mg Subcutaneous
Subject Risankizumab Monoclonal antibody 360 mg Subcutaneous