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Clinical trial intelligence report
Assessment of Dose-Dependent Effects of LY2189265 on Glycemic Control in Japanese Patients With Type 2 Diabetes
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT01001104-Jun 24, 2026
NCT ID
NCT01001104
Status
COMPLETED
Phase
Phase 2
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
LY2189265, a GLP-1 receptor agonist, is being evaluated for its efficacy in glycemic control among Japanese patients with Type 2 Diabetes. The competitive landscape includes other GLP-1 receptor agonists such as semaglutide and liraglutide, which have established market presence. Given the increasing prevalence of diabetes in Japan, successful outcomes could position Eli Lilly favorably in this growing market. Diligence should focus on the differentiation of LY2189265 in terms of efficacy, safety profile, and patient adherence compared to existing therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01001104
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
GLP-1 receptor
Intervention
LY2189265, 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.