Patient Guide: Mirikizumab Administered at the Same Time as Tirzepatide in Adult Participants With Moderately to Severely Active Ulcerative Colitis and Obesity or Overweight: Phase 3b Study

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 197 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06937086
Status: 🟢 Enrolling Now
Condition: Ulcerative Colitis, Obesity or Overweight
Phase: PHASE3

Where You Can Participate

This study is available at 197 locations across the country.

Top locations include:
  • • Dothan, Alabama
  • • Anaheim, California
  • • Beverly Hills, California
  • • And 194 more locations

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Mirikizumab Administered at the Same Time as Tirzepatide in Adult Participants With Moderately to Severely Active Ulcerative Colitis and Obesity or Overweight: Phase 3b Study - Join Clinical Trial NCTNCT06937086

How to Join This Clinical Trial - NCTNCT06937086

Learn how to participate in this PHASE3 trial studying an investigational therapy for Ulcerative Colitis, Obesity or Overweight. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Ulcerative Colitis, Obesity or Overweight
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06937086 - 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 197 locations. Find a study site near you:

Clinical Research Site

Dothan, Alabama 36301 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Anaheim, California 92806 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Beverly Hills, California 90211 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Los Alamitos, California 90720 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Northridge, California 91324 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Miami, Florida 33134 - United States

Status: RECRUITING

Clinical Research Site

Miami, Florida 33176 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Orlando, Florida 32806 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Orlando, Florida 32825 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Pensacola, Florida 32504 - United States

Status: NOT_YET_RECRUITING

And 187 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 Ulcerative Colitis, Obesity or Overweight:

  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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