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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

About this study

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

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Dulaglutide
PhasePhase 3
DrugDulaglutide
Primary goalNumber of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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