Patient Guide: A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 23 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07007637
Status: ENROLLING_BY_INVITATION
Condition: Hidradenitis Suppurativa
Phase: PHASE3

Where You Can Participate

This study is available at 23 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Northridge, California
  • • North Miami Beach, Florida
  • • And 20 more locations

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A Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of Subcutaneous Sonelokimab in Participants With Moderate to Severe Hidradenitis Suppurativa - Join Clinical Trial NCTNCT07007637

How to Join This Clinical Trial - NCTNCT07007637

Learn how to participate in this PHASE3 trial studying an investigational therapy for Hidradenitis Suppurativa. Current status: ENROLLING_BY_INVITATION.

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
PHASE3 - Large-scale efficacy study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT07007637 - 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 23 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35244 - United States

Status: Contact for availability

Clinical Research Site

Northridge, California 91325 - United States

Status: Contact for availability

Clinical Research Site

North Miami Beach, Florida 33162 - United States

Status: Contact for availability

Clinical Research Site

Macon, Georgia 31217 - United States

Status: Contact for availability

Clinical Research Site

Sandy Springs, Georgia 30328 - United States

Status: Contact for availability

Clinical Research Site

Columbus, Indiana 47201 - United States

Status: Contact for availability

Clinical Research Site

New Albany, Indiana 47150 - United States

Status: Contact for availability

Clinical Research Site

Murray, Kentucky 42071 - United States

Status: Contact for availability

Clinical Research Site

Canton, Michigan 48187 - United States

Status: Contact for availability

Clinical Research Site

Clarkston, Michigan 48346 - United States

Status: Contact for availability

And 13 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 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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