Evacetrapib and Cardiovascular Outcomes in High-Risk Vascular Disease
University of Adelaide · Sorbonne Université
Abstract
The cholesteryl ester transfer protein inhibitor evacetrapib substantially raises the high-density lipoprotein (HDL) cholesterol level, reduces the low-density lipoprotein (LDL) cholesterol level, and enhances cellular cholesterol efflux capacity. We sought to determine the effect of evacetrapib on major adverse cardiovascular outcomes in patients with high-risk vascular disease.
In a multicenter, randomized, double-blind, placebo-controlled phase 3 trial, we enrolled 12,092 patients who had at least one of the following conditions: an acute coronary syndrome within the previous 30 to 365 days, cerebrovascular atherosclerotic disease, peripheral vascular arterial disease, or diabetes mellitus with coronary artery disease. Patients were randomly assigned to receive either evacetrapib at a dose of 130 mg or matching placebo, administered daily, in addition to standard medical therapy. The primary efficacy end point was the first occurrence of any component of the composite of death from cardiovascular causes, myocardial infarction, stroke, coronary revascularization, or hospitalization for unstable angina.
Citation impact
- FWCI
- 87.01
- Percentile
- 100%
- References
- 35
Authors
29- AMA. Michael LincoffCorresponding
University of Adelaide, Sorbonne Université
- SJStephen J. Nicholls
Sorbonne Université, University of Adelaide
- JRJeffrey Riesmeyer
University of Adelaide, Sorbonne Université
- PJPhilip J. Barter
Sorbonne Université, University of Adelaide
- HBH Bryan Brewer
University of Adelaide, Sorbonne Université
Topics & keywords
- Medicine
- Coronary artery disease
- Internal medicine
- Placebo
- Clinical endpoint
- Stroke (engine)
- Myocardial infarction
- Diabetes mellitus
- Good health and well-being