LivingGLP1
Study S000055

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

Registration

Registration
NCT01664624
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
40
Start
2012-07
Primary completion
2012-11
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes
Interventions
DRUG:Roflumilast; DRUG:Alogliptin; DRUG:Exenatide; DRUG:Placebo to roflumilast; DRUG:Placebo to alogliptin
Results posted
TRUE
Secondary identifiers
REGISTRY:U1111-1128-6945

Registered primary outcomes

  • Change From Baseline in Postprandial Area Under the Curve From Time 0 to 8 Hours (AUC[0-8]) for Active Glucagon-like Peptide-1 [Baseline and Day 11; samples were taken at -15 min and -5 min (pre-meal), and 15 min, 30 min, and 1, 2, 3, 4, 6, and 8 hours (post-meal).]

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