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Clinical trial intelligence report
A Double Blind, Placebo-controlled, Dose-ranging Study to Investigate the Effect on Glycemic Control, Safety, Pharmacokinetics and Pharmacodynamics of GLP-1 in Patients With Type 2 Diabetes Mellitus Treated With a Stable Dose of Metformin.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00423501-Jul 28, 2026
NCT ID
NCT00423501
Status
COMPLETED
Phase
Phase 2
Sponsor
Hoffmann-La Roche
Executive brief
Investment-Ready Snapshot
The clinical trial conducted by Hoffmann-La Roche evaluates a GLP-1 analogue, taspoglutide, in patients with Type 2 Diabetes Mellitus who are on stable metformin therapy. Given the increasing prevalence of diabetes and the growing market for GLP-1 receptor agonists, successful outcomes could position taspoglutide favorably against established competitors such as liraglutide and semaglutide. The trial's completion and the anticipated efficacy and safety data will be critical for strategic positioning in a competitive landscape that includes both established and emerging therapies. The target population of 100-500 individuals indicates a robust dataset that could support regulatory filings and market entry strategies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00423501
Indication
Diabetes Mellitus Type 2
Modality
small molecule
Target
GLP-1 receptor
Intervention
Placebo, taspoglutide, taspoglutide, taspoglutide, taspoglutide, taspoglutide
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.