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Study details
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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)

Eli Lilly and Company
NCT IDNCT06739122ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

55

Study length

about 1.6 years

Ages

10–17

Locations

41 sites in AR, AZ, CA +23

What this study is about

Researchers are testing different doses of dulaglutide in children with type 2 diabetes. The trial will last about 8 months.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Dulaglutide

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

dulaglutide

Endpoints

Primary: Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration

Secondary: Change from Baseline in Hemoglobin A1c (HbA1c), Change from Baseline in Total Cholesterol, Change from Baseline in the EQ-5D-Y-5L, PK: Maximum Observed Concentration (Cmax) of Dulaglutide, Percent Change from Baseline in Body Weight, Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of Dulaglutide

Body systems

Endocrinology