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Clinical trial intelligence report
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
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06739122-Jul 28, 2026
NCT ID
NCT06739122
Status
RECRUITING
Phase
Phase 3
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
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.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06739122
Indication
Type 2 Diabetes
Modality
small molecule
Target
GLP-1 receptor agonist (Dulaglutide)
Intervention
Dulaglutide
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.