drugset / Trial / NCT01144338

Exenatide Study of Cardiovascular Event Lowering Trial (EXSCEL): A Trial To Evaluate Cardiovascular Outcomes After Treatment With Exenatide Once Weekly In Patients With Type 2 Diabetes Mellitus

NCT01144338 ↗

Phase 3 Completed 14752 enrolled AstraZeneca
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will compare the impact of including exenatide once weekly in addition to usual care vs. usual care without exenatide on major cardiovascular outcomes as measured by the primary composite endpoint of cardiovascular-related death, nonfatal myocardial infarction (MI), or nonfatal stroke.

Timeline

Start
2010-06-18
Primary completion
2017-04-21
Completion
2017-04-24

Outcome

Mixed primary results

registry analysis (superiority test); Placebo vs Exenatide Once Weekly; p = 0.061; Hazard Ratio (HR) 0.91 (95% CI 0.832 to 1.004); Regression, Cox NCT01144338 ↗

registry analysis (non-inferiority test); Placebo vs Exenatide Once Weekly; p < 0.001; Hazard Ratio (HR) 0.91 (95% CI 0.832 to 1.004); Regression, Cox NCT01144338 ↗

paper Noninferiority will be concluded if the upper limit of the CI is <1.30. PMID 26995376 ↗

release “The EXSCEL trial met its primary safety objective of non-inferiority for MACE.” astrazeneca.com ↗

release “although the primary efficacy objective of a superior reduction in MACE narrowly missed statistical significance (p=0.061).” astrazeneca.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Exenatide Peptide 2 mg Subcutaneous