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Study identifier: NCT07213973 Synced from ClinicalTrials.gov · July 30, 2026
● Recruiting

Pharmacokinetics, Safety, and Efficacy of Povorcitinib in Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa

Condition: Hidradenitis Suppurativa (HS)  ·  Sponsor: Incyte Corporation

PhasePhase 2
Planned participants40
Who can joinAll sexes, 12 Years to 17 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the pharmacokinetics, safety, and efficacy of povorcitinib in adolescent participants with moderate to severe hidradenitis suppurativa over a 54-week open-label treatment period.

This description comes directly from the study's public registry record.

Talk to the study team

Incyte Corporation Call Center (US)  ·  1.855.463.3463  ·  medinfo@incyte.com

Incyte Corporation Call Center (ex-US)  ·  +800 00027423  ·  eumedinfo@incyte.com

Always discuss trial participation with your own doctor first.

Locations (30)

University of Alabama At BirminghamBirmingham, Alabama, United StatesRecruiting
Medical Dermatology Specialists PhoenixPhoenix, Arizona, United StatesRecruiting
Saguaro DermatologyPhoenix, Arizona, United StatesRecruiting
Uconn HealthFarmington, Connecticut, United StatesRecruiting
University of Miami Miller School of MedicineMiami, Florida, United StatesRecruiting
Skin Research of South Florida, LlcMiami, Florida, United StatesRecruiting
Trueblue Clinical ResearchTampa, Florida, United StatesRecruiting
Advanced Medical Research PcSandy Springs, Georgia, United StatesRecruiting
Endeavor Health Medical GroupSkokie, Illinois, United StatesRecruiting
Dermatology Skin Cancer Center LeawoodLeawood, Kansas, United StatesRecruiting
Equity MedicalBowling Green, Kentucky, United StatesRecruiting
Johns Hopkins Univ Schl of MedicineBaltimore, Maryland, United StatesRecruiting

+ 18 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07213973