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

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 20 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07049575
Status: 🟢 Enrolling Now
Condition: Hidradenitis Suppurativa
Phase: PHASE1

Where You Can Participate

This study is available at 20 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • Fountain Valley, California
  • • Northridge, California
  • • And 17 more locations

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Study to Evaluate the Maximal Use of Ruxolitinib Cream in Adult and Adolescent Participants With Hidradenitis Suppurativa - Join Clinical Trial NCTNCT07049575

How to Join This Clinical Trial - NCTNCT07049575

Learn how to participate in this PHASE1 trial studying an investigational therapy for Hidradenitis Suppurativa. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Hidradenitis Suppurativa. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Hidradenitis Suppurativa
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT07049575 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 20 locations. Find a study site near you:

Clinical Research Site

Phoenix, Arizona 85008 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Fountain Valley, California 92708 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Northridge, California 91324 - United States

Status: RECRUITING

Clinical Research Site

Thousand Oaks, California 91320 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Castle Rock, Colorado 80109 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Sanford, Florida 32771 - United States

Status: RECRUITING

Clinical Research Site

Sweetwater, Florida 33172 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33609 - United States

Status: RECRUITING

Clinical Research Site

Columbus, Georgia 31904 - United States

Status: RECRUITING

Clinical Research Site

Bowling Green, Kentucky 42104 - United States

Status: RECRUITING

And 10 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Hidradenitis Suppurativa:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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