LivingGLP1
Study S001562

A Phase 3, Open-Label, Multicenter, Single-Arm Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Efficacy of Dulaglutide 3.0 mg and 4.5 mg in Pediatric Participants 10 to Less Than 18 Years of Age With Type 2 Diabetes Mellitus

Registration

Registration
NCT06739122
Study type
INTERVENTIONAL
Phase
PHASE3
Masking
NONE
Status
RECRUITING
Enrollment
55
Start
2025-01-10
Primary completion
2027-12
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes
Interventions
DRUG:Dulaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:H9X-MC-GBGS

Registered primary outcomes

  • Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug Administration [Baseline through Week 26]

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