A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS) (NCT06739122)
A Phase 3, Open-Label, Multicenter, Single-Arm Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Efficacy of Dulaglutide 3.0 mg and 4.5 mg in Pediatric Participants 10 to Less Than 18 Years of Age With Type 2 Diabetes Mellitus
๐ฉบ Plain-English Summary (8th-Grade Level)
The main purpose of this study is to evaluate additional dosing options for dulaglutide in pediatric participants with Type 2 Diabetes. Participation in this study will last about 8 months.
Who can join: Review the eligibility criteria below.
Location: University of Arizona โ Tucson, Arizona
Age range: 10 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 (51 Sites)
Showing the first 25 of 51 sites.
- University of Arizona โ Tucson, Arizona
- Arkansas Childrens Hospital โ Little Rock, Arkansas
- Division of Endocrinology, Diabetes, and Metabolism โ Los Angeles, California
- UCLA Mattel Children's Hospital โ Los Angeles, California
- University of California, San Francisco โ San Francisco, California
- Children's Hospital of Colorado โ Denver, Colorado
- Yale Diabetes Research โ New Haven, Connecticut
- Emerson Clinical Research Institute โ Washington D.C., District of Columbia
- Children's National Medical Center โ Washington D.C., District of Columbia
- Nemours Children's Health โ Jacksonville, Florida
- D&H National Research Centers, Inc โ Miami, Florida
- AdventHealth Orlando โ Orlando, Florida
- D&H Tamarac Research Center, LLC โ Tamarac, Florida
- University of South Florida โ Tampa, Florida
- Children's Healthcare of Atlanta - Center for Advanced Pediatrics โ Atlanta, Georgia
- Centricity Research Columbus Endocrinology โ Columbus, Georgia
- St. Luke's Children's Endocrinology and Diabetes โ Boise, Idaho
- University of Illinois at Chicago โ Chicago, Illinois
- Center for Diabetes and Metabolic Diseases Indiana University โ Indianapolis, Indiana
- University of Iowa Stead Family Children's Hospitals โ Iowa City, Iowa
- Norton Children's Endocrinology โ Louisville, Kentucky
- Johns Hopkins University School of Medicine โ Baltimore, Maryland
- University of Mississippi Medical Center โ Jackson, Mississippi
- University of New Mexico Hospital โ Albuquerque, New Mexico
- WBMD Pediatrics โ Buffalo, New York
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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Explore by condition: All Type 2 Diabetes clinical trials
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.