ReoPro Approved For Expanded Usage
The US Food and Drug Administration has approved Centocor/Eli Lilly's ReoPro (abciximab) for use in unstable angina patients who do not respond to conventional therapy and in whom a percutaneous coronary intervention (eg angioplasty, atherectomy or stent placement) is planned within 24 hours.
The agency also expanded its use to include a broad range of patients at risk of ischemic complications after PCI. The drug was originally approved only for high-risk patients undergoing angioplasty. The expanded labeling is based on the results of the EPILOG and CAPTURE trials (Marketletters passim).
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