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To Assess the Efficacy and Safety of INCB054707 in Participants With Hidradenitis Suppurativa
To evaluate the efficacy and safety of INCB054707 in participants with hidradenitis suppurativa over a 16-week placebo-controlled treatment period followed by a 36-week open-label extension period. All eligible participants will be invited to continue treatment for an additional 48-week Long-term extension period (also open label).
Details
| Lead sponsor | Incyte Corporation |
|---|---|
| Phase | PHASE2 |
| Status | COMPLETED |
| Enrolment | 209 |
| Start date | Tue Aug 25 2020 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Wed Aug 16 2023 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Hidradenitis Suppurativa
- Acne Inversa
Interventions
- INCB054707
- Placebo
Countries
France, Germany, Poland, Canada, United States, Spain