A Platform Trial for Pediatric Participants With Obesity or Overweight (LY900040) (NCT06672549)
A Master Protocol for a Randomized, Controlled, Clinical Platform Trial to Investigate the Efficacy and Safety of Interventions for Chronic Weight Management in Pediatric Participants With Obesity or Overweight
๐ฉบ Plain-English Summary (8th-Grade Level)
The purpose of this pediatric, chronic weight management, Phase 3 Master Protocol (PWMP) is to create a framework to evaluate the safety and efficacy of pharmacologic agents for the treatment of obesity or overweight in pediatric participants.
Who can join: Review the eligibility criteria below.
Location: University of Arizona โ Tucson, Arizona
Age range: 6 Years to 17 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (117 Sites)
Showing the first 25 of 117 sites.
- University of Arizona โ Tucson, Arizona
- Loma Linda University School of Medicine โ Loma Linda, California
- Childrens Hospital of Los Angeles โ Los Angeles, California
- UCLA Mattel Children's Hospital โ Los Angeles, California
- Children's Hospital of Orange County - Orange โ Orange, California
- Carey Chronis MD Pediatric, Infant and Adolescent Medicine โ Oxnard, California
- Children's Hospital Colorado โ Colorado Springs, Colorado
- Yale School of Medicine - Yale Diabetes Center (YDC)) Trials โ New Haven, Connecticut
- Stamford Therapeutics Consortium โ Stamford, Connecticut
- William A. Shands Hospital at the University of Florida โ Gainesville, Florida
- Florida Hospital- Center for Pediatric Research โ Orlando, Florida
- Nemours Children's Health โ Orlando, Florida
- All Childrens Hospital โ St. Petersburg, Florida
- Children's Healthcare of Atlanta - Center for Advanced Pediatrics โ Atlanta, Georgia
- Ann and Robert Lurie Children's Hospital of Chicago โ Chicago, Illinois
- University of Illinois at Chicago โ Chicago, Illinois
- Riley Hospital for Children โ Indianapolis, Indiana
- Norton Children's Endocrinology โ Louisville, Kentucky
- Velocity Clinical Research โ Lafayette, Louisiana
- Johns Hopkins Children's Center โ Baltimore, Maryland
- Boston Children's Hospital โ Boston, Massachusetts
- Helen Devos Childrens' Hospital - PIN โ Grand Rapids, Michigan
- University of Minnesota Masonic Children's Hospital โ Minneapolis, Minnesota
- Mayo Clinic - PIN โ Rochester, Minnesota
- Children's Minnesota Pediatric Endocrinology Clinic & McNeeley Diabetes Center โ Saint Paul, Minnesota
๐ 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.
๐ฐ 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 ยง 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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๐ก 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.