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Study to Evaluate the Maximal Use of Ruxolitinib Cream in Adult and Adolescent Participants With Hidradenitis Suppurativa

RecruitingPhase 1

A Maximal Use Trial of Ruxolitinib Cream in Adult and Adolescent Participants With Hidradenitis Suppurativa

Who can join

Ages 12 to 75 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Diagnosis of HS for at least 6 months before screening visit.
* Diagnosis of HS (Hurley Stage I, II, III) with a total abscess and inflammatory nodule count of at least 4 and affecting at least 3 distinct anatomical areas at screening and Day 1 visits.
* Total estimated treatment BSA \> 20% at screening and baseline.
* Agreement to not use topical or systemic antibiotics for treatment of HS during the Maximal Use Treatment Period.
* Willingness to avoid pregnancy or fathering children based on the criteria defined in the protocol.
* Further inclusion criteria apply.

Exclusion Criteria:

* Current or history of skin condition(s) other than HS that might confound the evaluation of HS; clinically uncontrolled cardiovascular disease; thrombosis; certain cancers; certain infections; severe anemia, thrombocytopenia, or neutropenia; other medical conditions at the discretion of the investigator.
* Laboratory values outside of the protocol-defined ranges.
* Further exclusion criteria apply.

About the study

The purpose of this study is to evaluate the maximal use of ruxolitinib cream in adult and adolescent participants with hidradenitis suppurativa.

What is being tested

Sponsor: Incyte Corporation · Participants: 24 · Started: Nov 3, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07049575

Locations in the U.S.

ArizonaSaguaro Dermatology, Phoenix
CaliforniaAmicis Research Center Valencia, Northridge
Children'S Hospital of Orange County, Orange
Clinical Trials Research Institute, Thousand Oaks
FloridaInternational Clinical Research Tennessee Llc, Sanford
Lenus Research Medical Group, Llc, Sweetwater
Trueblue Clinical Research, Tampa
GeorgiaLane Dermatology and Dermatologic Surgery, Columbus
IndianaOptions Research Group, Llc, West Lafayette
KentuckyEquity Medical, Llc, Bowling Green
LouisianaDelricht Research, Baton Rouge
MissouriRed River Research Partners, Bolivar
New YorkDr Bobby Buka, Md Greenwich Village, New York
Equity Medical, Llc, New York
North DakotaRed River Research Partners, Fargo
OklahomaUnity Clinical Research, Oklahoma City
PennsylvaniaPaddington Testing Co Inc, Philadelphia

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.