TrialSignal
Clinical trial intelligence report
A Phase 1b, Randomized, Double-Blind, Active Comparator (Open-Label Exenatide) Controlled Study to Evaluate the Effect of Roflumilast Plus Alogliptin on Postprandial Active GLP-1 Level and 24-hour Glucose Level in Subjects With Type 2 Diabetes Who Are Inadequately Controlled on a Stable Dose of Metformin
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01664624-Jul 28, 2026
NCT ID
NCT01664624
Status
COMPLETED
Phase
Phase 1b
Sponsor
AstraZeneca
Executive brief
Investment-Ready Snapshot
AstraZeneca's study evaluates the combination of roflumilast and alogliptin in patients with inadequately controlled Type 2 Diabetes Mellitus (T2DM) on metformin. The market for diabetes therapies is highly competitive, with a growing demand for innovative treatments that enhance glycemic control. The combination therapy could provide a differentiated offering in a crowded market, particularly if it demonstrates superior efficacy or safety compared to existing therapies. Diligence should focus on the potential for regulatory approval and market access strategies, as well as the competitive landscape, including other GLP-1 receptor agonists and DPP-4 inhibitors.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01664624
Indication
Type 2 Diabetes
Modality
small molecule
Target
Glucagon-like peptide-1 (GLP-1) receptor modulation
Intervention
Roflumilast, Alogliptin, Exenatide, Placebo to roflumilast, Placebo to alogliptin
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.