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
Eli Lilly's Phase 3 trial of Dulaglutide in pediatric patients with Type 2 Diabetes Mellitus aims to expand the therapeutic options for this demographic, which is increasingly affected by diabetes. The trial is currently recruiting and is expected to provide critical data on safety, efficacy, and pharmacokinetics. Given the rising prevalence of Type 2 diabetes among children and adolescents, successful outcomes could position Dulaglutide as a leading treatment option in this market segment. The competitive landscape includes other GLP-1 receptor agonists and diabetes therapies, necessitating a strong focus on differentiating factors such as dosing flexibility and safety profiles. Diligence should be exercised regarding regulatory pathways and potential market access challenges, particularly in pediatric populations.
Indication: Type 2 Diabetes
Modality: small molecule
Target: GLP-1 receptor agonist (Dulaglutide)
Sponsor: Eli Lilly and Company
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jul 11, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: GLP-1 receptor agonist (Dulaglutide)
View original source fields
Condition raw: Type 2 Diabetes
Condition normalized: Type 2 Diabetes
Modality raw: small molecule
Modality normalized: small molecule
Target raw: GLP-1 receptor agonist (Dulaglutide)
Target normalized: GLP-1 receptor agonist (Dulaglutide)