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.
Age range
10 Years – 17 Years
Sex
ALL
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Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration
Timeframe: Baseline through Week 26
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or