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To Assess the Efficacy and Safety of INCB054707 in Participants With Hidradenitis Suppurativa

NCT04476043 PHASE2 COMPLETED Results posted

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 sponsorIncyte Corporation
PhasePHASE2
StatusCOMPLETED
Enrolment209
Start dateTue Aug 25 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionWed Aug 16 2023 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

France, Germany, Poland, Canada, United States, Spain