Patient Guide: A Study of Orforglipron (LY3502970) in Adult Participants With Obesity or Overweight With Weight-Related Comorbidities

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 138 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05869903
Status: ACTIVE_NOT_RECRUITING
Condition: Obesity, Overweight, Overweight or Obesity
Phase: PHASE3

Where You Can Participate

This study is available at 138 locations across the country.

Top locations include:
  • • Chandler, Arizona
  • • Sun City West, Arizona
  • • Concord, California
  • • And 135 more locations

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A Study of Orforglipron (LY3502970) in Adult Participants With Obesity or Overweight With Weight-Related Comorbidities - Join Clinical Trial NCTNCT05869903

How to Join This Clinical Trial - NCTNCT05869903

Learn how to participate in this PHASE3 trial studying an investigational therapy for Obesity, Overweight, Overweight or Obesity. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Obesity, Overweight, Overweight or Obesity
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05869903 - 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 138 locations. Find a study site near you:

Clinical Research Site

Chandler, Arizona 85225 - United States

Status: Contact for availability

Clinical Research Site

Sun City West, Arizona 85375 - United States

Status: Contact for availability

Clinical Research Site

Concord, California 94520 - United States

Status: Contact for availability

Clinical Research Site

Escondido, California 92025 - United States

Status: Contact for availability

Clinical Research Site

Greenbrae, California 94904 - United States

Status: Contact for availability

Clinical Research Site

Huntington Park, California 90255 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90057 - United States

Status: Contact for availability

Clinical Research Site

Montclair, California 91763 - United States

Status: Contact for availability

Clinical Research Site

San Ramon, California 94583 - United States

Status: Contact for availability

Clinical Research Site

Tustin, California 92780 - United States

Status: Contact for availability

And 128 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 Obesity, Overweight, Overweight or Obesity:

  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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