TrialSignal
Clinical trial intelligence report
A Phase 2 Study of Once-Weekly LY3298176 Compared With Placebo and Dulaglutide in Patients With Type 2 Diabetes Mellitus
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03131687-Jul 28, 2026
NCT ID
NCT03131687
Status
COMPLETED
Phase
Phase 2
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
Eli Lilly's tirzepatide is positioned to compete in the growing Type 2 diabetes market, which is projected to reach $70 billion by 2025. The drug's once-weekly administration and dual receptor action may provide a competitive edge over existing therapies such as dulaglutide. Successful outcomes from this trial could enhance Eli Lilly's portfolio and market share, particularly against other GLP-1 receptor agonists. The trial's completion and subsequent data readouts will be critical for investor confidence and potential partnerships or licensing opportunities.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03131687
Indication
Type 2 Diabetes Mellitus
Modality
small molecule
Target
Tirzepatide (LY3298176) targets the glucagon-like peptide-1 receptor (GLP-1R) and the glucose-dependent insulinotropic polypeptide receptor (GIPR), enhancing insulin secretion and reducing glucagon levels in patients with Type 2 Diabetes Mellitus.
Intervention
tirzepatide, 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.