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Clinical trial intelligence report
A 24-week Multicenter, Open-label, Single-arm Study to Evaluate Safety in Patients With Type 2 Diabetes Mellitus in India Treated With Dulaglutide
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT05659537-Aug 04, 2026
NCT ID
NCT05659537
Status
COMPLETED
Phase
Phase 4
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
Eli Lilly's dulaglutide, a GLP-1 receptor agonist, is being evaluated for safety in a diverse population of patients with Type 2 Diabetes Mellitus (T2DM) in India. Given the increasing prevalence of diabetes in India, this study addresses a significant market need. The results could reinforce dulaglutide's position in the competitive landscape against other GLP-1 receptor agonists and oral antihyperglycemic agents. Successful outcomes may enhance market penetration and support further regulatory approvals in the region. Additionally, the study's completion and subsequent data publication will be critical for Eli Lilly's ongoing commercial strategy and investor confidence.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05659537
Indication
Diabetes Mellitus, Type 2
Modality
small molecule
Target
Glucagon-like peptide-1 receptor (GLP-1R)
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.