drugset / Trial / NCT03926169
A Global Study Comparing Risankizumab to Placebo in Adult Participants With Moderate to Severe Hidradenitis Suppurativa
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Risankizumab | Monoclonal antibody | 180 mg | Subcutaneous |
| Subject | Risankizumab | Monoclonal antibody | 360 mg | Subcutaneous |