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A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS)
NCT06739122 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Dulaglutide
Study Locations (20)
Florida
- Nemours Children's Health — Jacksonville
- D&H National Research Centers, Inc — Miami
- AdventHealth Orlando — Orlando
- D&H Tamarac Research Center, LLC — Tamarac
- University of South Florida — Tampa
California
- Division of Endocrinology, Diabetes, and Metabolism — Los Angeles
- UCLA Mattel Children's Hospital — Los Angeles
- University of California, San Francisco — San Francisco
District of Columbia
- Emerson Clinical Research Institute — Washington D.C.
- Children's National Medical Center — Washington D.C.
Georgia
- Children's Healthcare of Atlanta - Center for Advanced Pediatrics — Atlanta
- Centricity Research Columbus Endocrinology — Columbus
Arizona
- University of Arizona — Tucson
Arkansas
- Arkansas Childrens Hospital — Little Rock
Colorado
- Children's Hospital of Colorado — Denver
Connecticut
- Yale Diabetes Research — New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 55 participants |
| Start Date | 2025-01-10 |
| Est. Completion | 2027-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06739122
The ClinicalTrials.gov registry entry for NCT06739122 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 55 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Type 2 Diabetes appearing as the primary indexed condition, and to 1 intervention — of which Dulaglutide is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06739122 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Florida, California, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06739122 about?
NCT06739122 is a clinical study titled "A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS)". 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.
What is the current status of trial NCT06739122?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 55 participants. The study started on 2025-01-10. Estimated completion is 2027-12.
What conditions does trial NCT06739122 study?
This clinical trial studies the following conditions: Type 2 Diabetes. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06739122?
The interventions under investigation include: Dulaglutide (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06739122?
This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06739122 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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