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CAPTURE: C 7E3 Fab A nti- P latelet T herapy in U nstable RE fractory Angina

CAPTURE: C 7E3 Fab A nti- P latelet T herapy in U nstable RE fractory Angina.

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CAPTURE: C 7E3 Fab A nti- P latelet T herapy in U nstable RE fractory Angina

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  1. CAPTURE:C7E3FabAnti-PlateletTherapy in Unstable REfractory Angina • Study Population: Patients with chest pain at rest and ECG signs of UA (NQMI excluded) proven refractory to 2-48 hours of heparin and nitroglycerin and determined eligible via diagnostic catheterization for PCI within 18-24 hours • Dosing arms: ASA + standard-dose, weight-adjusted heparin - abciximab 0.25 mg/kg bolus + 10 µg/min infusion for 18-24 hours pre-PCI and 1 hour post-PCI (n=630) - placebo (n=635) • Primary endpoint: Death, MI, or urgent repeat intervention at 30 days The CAPTURE Investigators. Lancet. 1997; 349: 1429-1435.

  2. CAPTUREStudy design heparin + nitroglycerin ASA + heparin + abciximab Diagnostic catheterization confirming eligibility for PCI PCI • Diagnosis of refractory UA • Chest pain with ECG signs of ischemia with heparin + nitroglycerin • Diagnosis of UA • Chest pain with ECG signs of ischemia (non-Q-wave MI excluded) 2 - 48 hours 18 - 24 hours 1 hour pre-PCI post-PCI The CAPTURE Investigators. Lancet. 1997; 349: 1429-1435.

  3. CAPTUREEfficacy results summary Endpoint Death, MI, or urgent repeat interventionDeath, MI, or anyrevascularizationDeathMIUrgent repeat intervention Anyrevascularization Time30 days 6 months30 days6 months Pre-PCI30 days6 months30 days6 months Placebo(n=635) 15.9% 30.8%1.3%2.2% 2.1%8.2%9.3% 10.9%24.9% Abciximab (n=630) 11.3% 31.0%1.0%2.8% 0.6%4.1%6.6% 7.8%25.4% P value vsplacebo 0.012 nsnsns0.0290.002ns nsns The CAPTURE Investigators. Lancet. 1997; 349: 1429-1435.

  4. CAPTURESafety results summary Safety endpoint Major TIMI bleedingMinor TIMI bleedingPlatelet count< 100,000/mm3 Placebo(n=635) 1.9%2.0%1.3% Abciximab(n=630) 3.8%4.8%5.6% The CAPTURE Investigators. Lancet. 1997; 349: 1429-1435.

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