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Abbott to Present New Data Across its Vascular Portfolio at the,,,American College of Cardiology's 56th Annual Scientific Session

limus Eluting Coronary Stent System with Boston Scientific's TAXUS Paclitaxel- Eluting Coronary Stent System. The primary endpoint of the trial is in-segment late loss at 240 days. The major secondary endpoint of the randomized portion of the trial is ischemia driven target vessel failure at 270 days. The results from SPIRIT III are intended to support approval of the XIENCE V Stent System by the U.S. Food and Drug Administration (FDA) and Japan's Ministry of Health, Labour and Welfare.

ABSORB: Bioabsorbable Clinical Trial Six-Month Data Results

Late-Breaking Clinical Trials I, i2. Summit Interventional Programming Saturday, March 24, 11 a.m. Central Time

Room La Nouvelle Orleans C, Ernest N. Morial Convention Center

Abbott's ABSORB study is the world's first clinical trial designed to evaluate the safety and performance of a fully bioabsorbable everolimus- eluting coronary stent platform. Patrick W. Serruys, M.D., Ph.D., of the Thoraxcentre, Erasmus University Hospital, Rotterdam, will present six-month clinical and angiographic results from the first 30 patients enrolled in the study.

Late-Breaking Clinical Trials I Press Conference at ACC

SPIRIT III data and ABSORB results will be included in the ACC late- breaking trials press conference I being held at noon Central time on Saturday, March 24, in Press Conference Room 215.

Abbott Investor Meeting and Webcast

Saturday, March 24, 1:30 p.m. Central Time

Abbott will host an investor meeting on Saturday, March 24, at 1:30 p.m. Central time to review the results of its Xience V SPIRIT and ABSORB bioabsorbable stent clinical trials. A live audio webcast of the meeting will be accessible through Abbott's Investor Relations Web site at www.abbottinvestor.com. An archived edition of the presentation will be available later that day.'"/>




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