February 23rd, 2012

FDA Grants MI Indication for Drug-Eluting Stents

Boston Scientific announced on Wednesday that the FDA had approved the use of its Ion and Taxus Liberte paclitaxel-eluting stents for the treatment of patients with MI. These are the first drug-eluting stents to receive a specific indication for MI.

The new indication is based on data from the Taxus clinical program and the HORIZONS-AMI trial. Acute MI accounts for about 10% of  coronary interventions, according to the company.

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