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Cordis announces clinical and educational programs for CYPHER Sirolimus-eluting Coronary Stent

Published in Medical Letter on the CDC and FDA, January 7th, 2007

Cordis Corporation stated to an advisory panel to the U.S. Food and Drug Administration (FDA) that analysis of its research on the CYPHER Sirolimus-eluting Coronary Stent suggests a need for additional education on anti-platelet therapy regimens for bare-metal and drug-eluting stent patients and further research to understand safety factors.

Further, Cordis committed to support efforts by the clinical community, medical societies and industry to achieve these goals. The company's conclusions are based on an independent analysis of long-term clinical data for the CYPHER Stent that were presented recently.

This independent analysis, conducted and...

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