A Master Protocol Study (LY900038) of Multiple Intervention-Specific-Appendices (ISAs) in Adult Participants With Obesity or Overweight (NCT06143956)
A Master Protocol for a Randomized, Controlled, Clinical Trial of Multiple Interventions for Chronic Weight Management in Adult Participants With Obesity or Overweight
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this Phase-2 chronic weight management master protocol (CWMM) is to create a framework to evaluate the safety and efficacy of various investigational interventions for chronic weight management with intervention-specific appendices (ISAs). The CWMM establishes entry criteria for newly enrolled participants across the master and the ISAs. The ISAs may start independently of other ISAs as interventions become available for clinical testing. The results for the CWMM screening record will be reported when all the ISA's complete.
Who can join: Review the eligibility criteria below.
Location: The Institute for Liver Health II dba Arizona Clinical Trials - Mesa — Chandler, Arizona
Age range: 18 Years to 75 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (54 Sites)
Showing the first 25 of 54 sites.
- The Institute for Liver Health II dba Arizona Clinical Trials - Mesa — Chandler, Arizona
- HOPE Research Institute — Phoenix, Arizona
- Headlands Research - Scottsdale — Scottsdale, Arizona
- The Institute for Liver Health II dba Arizona Liver Health-Tucson — Tucson, Arizona
- NorCal Medical Research, Inc — Greenbrae, California
- Velocity Clinical Research, Huntington Park — Huntington Park, California
- Peninsula Research Associates — Rolling Hills Estates, California
- Diablo Clinical Research, Inc. — Walnut Creek, California
- Stamford Therapeutics Consortium — Stamford, Connecticut
- Northeast Research Institute (NERI) — Fleming Island, Florida
- New Horizon Research Center — Miami, Florida
- Indago Research & Health Center, Inc — Miami Lakes, Florida
- Suncoast Clinical Research, Inc. — New Port Richey, Florida
- Charter Research - Winter Park — Orlando, Florida
- Charter Research - Lady Lake — The Villages, Florida
- Pacific Diabetes & Endocrine Center — Honolulu, Hawaii
- Medical Research Partners — Ammon, Idaho
- Great Lakes Clinical Trials - Ravenswood — Chicago, Illinois
- Great Lakes Clinical Trials - Ravenswood — Chicago, Illinois
- NorthShore University Health System — Skokie, Illinois
- Iowa Diabetes and Endocrinology Research Center — West Des Moines, Iowa
- Cotton O'Neil Diabetes & Endocrinology — Topeka, Kansas
- Monroe Biomedical Research - Louisville — Louisville, Kentucky
- Knownwell — Needham, Massachusetts
- Lucida Clinical Trials — New Bedford, Massachusetts
📞 Contact the Study Coordinator
Phone: (317) 615-4559
Email: LillyTrials@Lilly.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.