drugset / Trial / NCT01687998

A Study of Evacetrapib in High-Risk Vascular Disease

NCT01687998 ↗

Phase 3 Terminated 12092 enrolled Eli Lilly and Company The Cleveland Clinic · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the ACCELERATE study is to evaluate the efficacy and safety of evacetrapib in participants with high-risk vascular disease (HRVD).

Timeline

Start
2012-10
Primary completion
2016-03
Completion
2016-07

Outcome

Missed primary endpoint

Stopped: “Study termination due to insufficient efficacy.”

registry Evacetrapib vs Placebo; p = 0.9054; Hazard Ratio (HR) 1.006 (95% CI 0.911 to 1.111) NCT01687998 ↗

paper a primary end-point event occurred in 12.9% of the patients in the evacetrapib group and in 12.8% of those in the placebo group PMID 28514624 ↗

paper treatment with evacetrapib did not result in a lower rate of cardiovascular events than placebo among patients with high-risk vascular disease. PMID 28514624 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Evacetrapib Small molecule 130 mg Oral