TrialSignal
Clinical trial intelligence report
A 56-week, Multicenter, Open-label, Active-controlled, Randomized Study to Evaluate the Efficacy and Safety of Efpeglenatide Once Weekly Compared to Dulaglutide Once Weekly in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 18, 2026
NCT ID
NCT03684642
Status
TERMINATED
Phase
Phase 3
Sponsor
Sanofi
Executive brief
Investment-Ready Snapshot
Efpeglenatide, developed by Sanofi, is positioned as a once-weekly GLP-1 receptor agonist for the treatment of Type 2 Diabetes Mellitus (T2DM). The asset aims to demonstrate non-inferiority to Dulaglutide, a well-established competitor in the GLP-1 market. The termination of the trial was due to a sponsor decision rather than safety concerns, which may indicate strategic repositioning or resource allocation towards other assets. The competitive landscape includes other GLP-1 therapies, and successful outcomes could enhance market share in a growing diabetes treatment market, which is projected to expand significantly due to increasing prevalence of diabetes globally.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03684642
Indication
Type 2 Diabetes Mellitus
Modality
small molecule
Target
GLP-1 receptor agonist
Intervention
Efpeglenatide, Dulaglutide, Background therapy Metformin
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.