Patient Guide: A Study to Assess the Efficacy and Safety of Induction and Maintenance Therapy With Afimkibart (RO7790121) in Participants With Moderately to Severely Active Crohn's Disease

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 181 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06819878
Status: 🟢 Enrolling Now
Condition: Moderately to Severely Active Crohns Disease
Phase: PHASE3

Where You Can Participate

This study is available at 181 locations across the country.

Top locations include:
  • • Dothan, Alabama
  • • Sun City, Arizona
  • • Garden Grove, California
  • • And 178 more locations

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A Study to Assess the Efficacy and Safety of Induction and Maintenance Therapy With Afimkibart (RO7790121) in Participants With Moderately to Severely Active Crohn's Disease - Join Clinical Trial NCTNCT06819878

How to Join This Clinical Trial - NCTNCT06819878

Learn how to participate in this PHASE3 trial studying an investigational therapy for Moderately to Severely Active Crohns Disease. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Moderately to Severely Active Crohns Disease
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06819878 - 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 181 locations. Find a study site near you:

Clinical Research Site

Dothan, Alabama 36305 - United States

Status: RECRUITING

Clinical Research Site

Sun City, Arizona 85351 - United States

Status: RECRUITING

Clinical Research Site

Garden Grove, California 92845-2006 - United States

Status: RECRUITING

Clinical Research Site

Inglewood, California 90301 - United States

Status: RECRUITING

Clinical Research Site

Lancaster, California 93534 - United States

Status: RECRUITING

Clinical Research Site

Lancaster, California 93534 - United States

Status: RECRUITING

Clinical Research Site

Los Alamitos, California 90720 - United States

Status: RECRUITING

Clinical Research Site

San Diego, California 92120 - United States

Status: RECRUITING

Clinical Research Site

San Francisco, California 94115 - United States

Status: RECRUITING

Clinical Research Site

Littleton, Colorado 80120 - United States

Status: RECRUITING

And 171 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 Moderately to Severely Active Crohns Disease:

  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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