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FDA Contributes Funds To Industry Post-Stenting Antiplatelet Trial

This article was originally published in The Gray Sheet

Executive Summary

FDA is contributing $1.5 million to a large, collaborative clinical study designed to find out the optimum length of time to give anti-clotting drugs to patients with coronary drug-eluting stents

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With cost and time commitments ballooning for device and drug clinical development, some prominent researchers are pressing for companies with similar products to join together on new FDA pivotal trials rather than go it alone.

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