INCB018424-324 Enrolling

Mild to Moderate Hidradenitis Suppurativa Research Trial (60 Weeks)


Treatment: Topical Age: 12 Years


Who Can Participate?
Adolescents and adults aged 12 years or older with hidradenitis suppurativa (HS), may be eligible.

Inclusion Criteria:
• Diagnosis of HS for at least 6 months
• At least 4 painful lumps under the skin (abscess and/or inflammatory nodules), with no draining tunnels, and affecting
at least 2 different body areas

Participant Info:
• No cost to participate or receive study treatment
• Regular visits with study doctors who are familiar with hidradenitis suppurativa
• Will receive investigational topical medication (active study drug) or placebo
• Reimbursement for study-related expenses may be provided

How Long Will The Study Last?
• Participation will last about 60 weeks and involve about 17 visits to the study research site


Participating Locations

Participating Experts

No Doctors Found

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The following information is from ClinicalTrials.gov

Last Update Posted: August 13, 2025

Official Title

A Phase 3, Double-Blind, Randomized, Vehicle-Controlled, Efficacy and Safety Study of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa

ClinicalTrials.gov ID

NCT06959225

Sponsor

Incyte Corporation

Study Description

  • Brief Summary:

    The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in participants with hidradenitis suppurativa.

  • Condition or Disease:

    Hidradenitis Suppurativa

  • Intervention/Treatment:

    Drug: Ruxolitinib Cream Drug: Vehicle Cream
  • Phase:

    PHASE3

  • Ages Eligible for Study:

    12 Years and older (CHILD,ADULT,OLDER_ADULT)

  • Sexes Eligible for Study:

    ALL


Terms and Conditions – ClinicalTrials.gov
Purpose of ClinicalTrials.gov Database. The U.S. National Institutes of Health, Department of Health and Human Services, through its National Library of Medicine, has developed ClinicalTrials.gov to provide patients, family members, and members of the public current information about clinical research studies.



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