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Long–term data presented from the SPIRIT III pivotal U.S. clinical trial demonstrated that the observed clinical advantages of Abbott's market–leading XIENCE V Everolimus Eluting Coronary Stent System continued to increase as compared to the TAXUS Express2 Paclitaxel–Eluting Coronary Stent System. At three years, XIENCE V demonstrated a 43 percent reduction in the risk of major adverse cardiac events compared to TAXUS (9.1 percent for XIENCE V vs. 15.7 percent for TAXUS, p–value=0.003)*.


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