INCB018424-325 Enrolling

Hidradenitis Suppurativa Study (approximately 60 Weeks)


Treatment: Topical Age: 12 Years


Who Can Participate?
Anybody aged 12 and above with HS may participate.

Inclusion Criteria
• have a diagnosis of HS for at least 6 months
• not have body areas to be treated exceed 20% of the total Body surface area

Participant Information
• Participate and receive study treatment at no cost
• Regular visits with study doctors who specialise in treating hidradenitis suppurativa (16 visits)
• Will receive an investigative topical treatment (study drug)
• Reimbursement for study-related expenses may be provided

How Long Will The Study Last?
• Approximately 60 weeks


Participating Locations

COUNTRY
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Canada

Participating Experts

No Doctors Found

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The following information is from ClinicalTrials.gov

Last Update Posted: August 12, 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

NCT06958211

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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Hidradenitis Suppurativa

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