RecruitingType 2 Diabetes

A Study of Dulaglutide (LY2189265) 3.0 mg and 4.5 mg in Pediatric Participants With Type 2 Diabetes Mellitus (AWARD-PEDS PLUS)

Eligible age

10–17 yrs

Accepts

All genders

Locations

26 states

Healthy volunteers

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About this study

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.

Sponsor: Eli Lilly and Company

You may qualify if…

✓ Have Type 2 diabetes treated with diet and exercise and metformin and/or basal insulin. Metformin and/or basal insulin dose must be stable for at least 8 weeks prior to screening.
✓ Have a body weight ≥50 kilograms (kg) and Body Mass Index (BMI) of \>85th percentile

You may not qualify if…

✕ Have Type 1 diabetes
✕ Have received treatment with any glucose-lowering agent(s) other than metformin, basal insulin, or dulaglutide within 8 weeks prior to screening
✕ After the Type 2 diabetes diagnosis, have a history of diabetic ketoacidosis or hyperosmolar syndrome
✕ Have had ≥1 episode of severe hypoglycemia and/or ≥1 episode of hypoglycemic unawareness within the last 6 months
✕ Have family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN2)
✕ Have prior chronic, recurrent, or idiopathic pancreatitis, or known gallbladder disease
✕ Have been treated with prescription drugs or over-the-counter medications that promote weight loss within 8 weeks prior to screening