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Boston Scientific Announces Schedule for EuroPcr 2007

ubgroups including patients with long lesions, overlapping stents, and small vessels. The Company plans to issue a press release at this time. * Predictors of Stent Thrombosis in real-world use. Two-year results from the ARRIVE 1 registry and pooled one-year data from ARRIVE 1 & 2 will be presented by David Dobies, M.D., F.A.C.C., at 5:07 p.m. in a late- breaking session. Data will focus on predictors of stent thrombosis in real-world patients treated with drug-eluting stents. The Company plans to issue a press release at this time. * SYNTAX Trial update. In a late-breaking trial session at 5:46 p.m., Patrick Serruys, M.D., will present final enrollment numbers for SYNTAX, a randomized, controlled clinical trial with nested registries designed to compare 12-month MACCE rates between the company's TAXUS(R) Express2(TM) paclitaxel-eluting coronary stent system and coronary artery bypass graft (CABG) treatment. The trial will study patients with three vessel disease and/or left main disease, a level of patient and lesion complexity not examined in prior DES studies. SYNTAX recently completed enrollment of more than 3,000 patients at 85 sites in Europe and the United States. * SPIRIT Trial Results -- XIENCE(TM) V (PROMUS(TM)) Stent and TAXUS Stent. At 6:17 p.m., results from Abbott's SPIRIT I, II and III clinical trials will be presented by Gregg W. Stone, M.D., at a late-breaking trial session. In addition to a three-year update on the SPIRIT FIRST trial results, Dr. Stone will provide a meta-analysis of data from patients in SPIRIT II and SPIRIT III treated with the XIENCE V (PROMUS) Stent or the TAXUS Express2 Stent. The SPIRIT family of trials is designed to evaluate the XIENCE V Everolimus-Eluting Coronary Stent System, manufactured and sold by Abbott, and also marketed
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