drugset / Trial / NCT00385138

Cangrelor Versus Standard Therapy to Achieve Optimal Management of Platelet Inhibition.

NCT00385138 ↗

Phase 3 Terminated 5364 enrolled The Medicines Company
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective of this study is to demonstrate that the efficacy of cangrelor (combined with usual care) is superior to that of usual care, in subjects requiring percutaneous coronary intervention (PCI) as measured by a composite of all-cause mortality, myocardial infarction (MI), and ischemia-driven revascularization (IDR).

Timeline

Start
2006-09
Primary completion
2009-05
Completion
2010-06

Outcome

Missed primary endpoint

Stopped: “Insufficient evidence of the clinical effectiveness of cangrelor”

paper The use of periprocedural cangrelor during PCI was not superior to placebo in reducing the primary end point. PMID 19915222 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cangrelor Small molecule 4 ug/kg Intravenous
Background Clopidogrel Small molecule 600 mg —