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Clinical trial intelligence report
A Randomized, Double-Blind Study With an Open-Label Extension Comparing the Effect of Once-Weekly Dulaglutide With Placebo in Pediatric Patients With Type 2 Diabetes Mellitus (AWARD-PEDS: Assessment of Weekly AdministRation of LY2189265 in Diabetes-PEDiatric Study)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02963766-Jul 28, 2026
NCT ID
NCT02963766
Status
COMPLETED
Phase
Phase 3
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
Eli Lilly's dulaglutide, a GLP-1 receptor agonist, is being evaluated for pediatric patients with type 2 diabetes mellitus. The pediatric diabetes market is expanding, driven by rising prevalence rates and increasing awareness of diabetes management in children. If successful, dulaglutide could capture significant market share, competing against other GLP-1 receptor agonists and diabetes therapies. The completion of this trial may enhance Eli Lilly's portfolio and strengthen its position in the diabetes market, particularly in the pediatric segment, which is currently underserved. Diligence should focus on potential regulatory hurdles and the competitive landscape, including emerging therapies targeting similar patient populations.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02963766
Indication
Type 2 Diabetes
Modality
small molecule
Target
Glucagon-like peptide-1 (GLP-1) receptor
Intervention
Dulaglutide, Placebo
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.