A Clinical Trial to Demonstrate the Efficacy of Cangrelor

PHASE3TerminatedINTERVENTIONAL
Enrollment

8,882

Participants

Timeline

Start Date

April 30, 2006

Primary Completion Date

May 31, 2009

Study Completion Date

June 30, 2010

Conditions
Myocardial Infarction (MI)Acute Coronary Syndromes (ACS)
Interventions
DRUG

Cangrelor (P2Y12 inhibitor)

IV bolus (30 mcg/kg) \& infusion (4 mcg/kg/min) initiated prior to PCI, as soon as possible following randomization (after need for PCI is confirmed) but not more than 30 minutes prior to placement of arterial access. Infusion is to continue for at least 2 hours, or until the end of the PCI, whichever is longer with the option to extend up to 4 hours maximum (per investigator discretion).

DRUG

clopidogrel (oral P2Y12 inhibitor)

600 mg active clopidogrel administered as soon as possible following randomization (after need for PCI confirmed), but not more than 30 minutes prior to the placement of the arterial access.

DRUG

Placebo bolus & placebo infusion

placebo bolus (30 mcg/kg) \& placebo infusion (4 mcg/kg/min) administered from randomization for at least 2 hours, or until the end of the PCI, whichever is longer with the option to extend up to 4 hours maximum (per investigator discretion)

DRUG

Placebo capsules - end of infusion

Placebo capsules given at the end of infusion to mimic 600mg clopidogrel dosing

DRUG

Placebo capsules - as soon as possible after randomization

Placebo capsules given as soon as possible after randomization to mimic 600mg clopidogrel dosing

Trial Locations (1)

19107-6192

Pennsylvania Hospital, Philadelphia

Sponsors
All Listed Sponsors
lead

The Medicines Company

INDUSTRY

NCT00305162 - A Clinical Trial to Demonstrate the Efficacy of Cangrelor | Biotech Hunter | Biotech Hunter