drugset / Trial / NCT01442038

Ranolazine for Incomplete Vessel Revascularization Post-Percutaneous Coronary Intervention (PCI)

NCT01442038 ↗

Phase 3 Completed 2651 enrolled Gilead Sciences
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will evaluate the efficacy of ranolazine as compared with placebo when used as part of standard medical therapy in chronic angina subjects with incomplete revascularization post-percutaneous coronary intervention (PCI; formerly known as angioplasty with stent) on the composite of ischemia-driven revascularization or ischemia-driven hospitalization without revascularization.

Timeline

Start
2011-10
Primary completion
2015-02
Completion
2015-02

Outcome

Missed primary endpoint

registry analysis (superiority or other test); Ranolazine vs Placebo; p = 0.48; Hazard Ratio (HR) 0.948 (95% CI 0.818 to 1.099) NCT01442038 ↗

paper Ranolazine did not reduce the composite rate of ischaemia-driven revascularisation or hospitalisation without revascularisation PMID 26474810 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranolazine Small molecule 500 mg Oral
Subject Ranolazine Small molecule 1000 mg Oral