drugset / Trial / NCT02229383

Phase III Study to Evaluate Safety and Efficacy of Added Exenatide Versus Placebo to Titrated Basal Insulin Glargine in Inadequately Controlled Patients With Type II Diabetes Mellitus

NCT02229383

Phase 3 Completed 464 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

Study D5553C00002 is a multicenter, randomized, double-blind, placebo-controlled, parallel group, Phase 3 study to compare the safety and efficacy of exenatide once weekly (EQW) added to titrated basal insulin glargine with or without metformin to placebo added to titrated basal insulin glargine with or without metformin in patients with type 2 diabetes mellitus (T2DM). Eligible patients will be randomized at Visit 5 (Day 1) to receive either EQW added to titrated basal insulin glargine, with or without metformin ≥1500 mg/day, or placebo added to titrated basal insulin glargine, with or without metformin ≥1500 mg/day, during the 28-week treatment period.

Timeline

Start
2014-09-06
Primary completion
2016-08-29
Completion
2016-08-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Exenatide Peptide 2 mg

Indications