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Boston Scientific Announces Schedule of Events at TCT Scientific Symposium
Date:11/1/2011

#160;Presentations will examine clinical data from challenging PCI subsets and preview new research on bioabsorbable drug delivery from the EVOLVE trial.
  • REPRISE Clinical Program for Lotus™ Valve System.  Ian Meredith, M.B.B.S., Ph.D., will present an update on the REPRISE clinical program, which is evaluating the Lotus™ Valve System, the first fully repositionable device for percutaneous aortic valve replacement to treat patients with severe aortic stenosis.  The Lotus Valve was developed by Sadra Medical, acquired by Boston Scientific in 2011.  The spotlight session begins at 8:58 a.m. in Room 135.  

    • Friday, November 11

  • Late-Breaking Trial: EVOLVE Endpoint Data.  Principal Investigator Ian Meredith, M.B.B.S., Ph.D., will present primary endpoint data from the EVOLVE trial during a late-breaking clinical session at 11 a.m. in the Main Arena.  EVOLVE is a prospective, randomized, non-inferiority trial that compares two dose formulations of everolimus on Boston Scientific's SYNERGY Coronary Stent to the PROMUS Element Everolimus-Eluting Coronary Stent in patients with de novo coronary artery lesions.  The SYNERGY Stent features the Company's proprietary platinum chromium alloy and uses a bioabsorbable polymer and everolimus drug combination to create an ultra-thin, uniform coating confined to the outer surface of the stent.  The Company plans to issue a press release announcing trial results at the conclusion of the presentation.

  • Late-Breaking Trial: COBRA Endpoint Data.   Subhash Banerjee, M.D., will present 12-month endpoint data from the COBRA trial during a late-breaking clinical session at 12:40 p.m. in the Main Arena.  COBRA is a prospective, randomized, multi-center trial that compares CryoPlasty® Therapy using the PolarCath™ Peripheral Dilatation System to conventional balloon angioplasty for the post-dilatation of
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