Patient Guide: Study to Evaluate Tulisokibart for Hidradenitis Suppurativa (MK-7240-012)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 21 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06956235
Status: 🟢 Enrolling Now
Condition: Hidradenitis Suppurativa
Phase: PHASE2

Where You Can Participate

This study is available at 21 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Phoenix, Arizona
  • • Northridge, California
  • • And 18 more locations

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Study to Evaluate Tulisokibart for Hidradenitis Suppurativa (MK-7240-012) - Join Clinical Trial NCTNCT06956235

How to Join This Clinical Trial - NCTNCT06956235

Learn how to participate in this PHASE2 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
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06956235 - 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 21 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35244 - United States

Status: RECRUITING

Clinical Research Site

Phoenix, Arizona 85006 - United States

Status: RECRUITING

Clinical Research Site

Northridge, California 91325 - United States

Status: RECRUITING

Clinical Research Site

Sacramento, California 95815 - United States

Status: RECRUITING

Clinical Research Site

Macon, Georgia 31217 - United States

Status: RECRUITING

Clinical Research Site

Indianapolis, Indiana 46250 - United States

Status: RECRUITING

Clinical Research Site

Troy, Michigan 48084 - United States

Status: RECRUITING

Clinical Research Site

Charlotte, North Carolina 28211 - United States

Status: RECRUITING

Clinical Research Site

Fairborn, Ohio 45324 - United States

Status: RECRUITING

Clinical Research Site

Anderson, South Carolina 29621 - United States

Status: RECRUITING

And 11 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 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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