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ClOpidogrel - bienvenue sur le site de l'amiform

ClOpidogrel - bienvenue sur le site de l'amiform

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Can PLATe<strong>le</strong>t Inhibition be Optimized to<br />

Prevent Vascular Events: PLATO<br />

~18,000 patients within 24 hours of<br />

an in<strong>de</strong>x ACS (STEMI or NSTEMI)<br />

AZD6140 90mg BID<br />

ASA 75-100mg QD<br />

Doub<strong>le</strong>-blind, doub<strong>le</strong>-dummy<br />

Mean f/u ~12.5 months. Range 6-24<br />

Clopidogrel 75mg QID<br />

Primary Endpoint: Time to first occurrence of the<br />

compo<strong>site</strong> of <strong>de</strong>ath, MI or stroke.<br />

Primary Safety Endpoint: Major b<strong>le</strong>eding<br />

At <strong>le</strong>ast 2 inclusion criteria:<br />

1. ST segment changes<br />

biomarkers<br />

2. At <strong>le</strong>ast 1:<br />

- >60 yo<br />

- Previous MI/CABG<br />

- Known > 1 Vessel CAD<br />

- AODM<br />

- PVD<br />

-Renal dysfunction<br />

AODM, adult-onset diabetes mellitus; PVD, peripheral vascular disease.<br />

Wal<strong>le</strong>ntin L, et al., for the PLATO study. A Comparison of AZD6140 and Clopidogrel in Patients With Acute<br />

Coronary Syndrome. Washington, DC. US Food and Drug Administration. Availab<strong>le</strong> at: http://clinicaltrials.gov.

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