DURHAM, N.C.–(BUSINESS WIRE)–Tryton Medical’s TRYTON Side Branch Stent™ System was discussed as an
      important new therapeutic option for patients with bifurcation disease
      last week at the annual European Bifurcation Club (EBC) meeting in
      Lisbon, Portugal, where approximately 150 international interventional
      cardiologists gathered to share best practices for challenging
      bifurcation cases.
    
      Patrick W. Serruys, M.D., Ph.D., of Erasmus Medical Center in Rotterdam,
      the Netherlands, presented an overview of the Tryton stent system,
      highlighting results from a number of studies of the device and the
      growing body of clinical evidence supporting the use of the Tryton stent
      system.
    
      “In a straw poll conducted at the EBC Meeting two years ago, Tryton was
      selected the dedicated stent of choice by a large margin. The
      accumulation of clinical data in more than 700 patients, with a rate of
      target lesion revascularization consistently less than four percent at
      six months, further validates Tryton’s leadership position,” said Prof.
      Serruys. “I am particularly excited about the potential of Tryton
      technology for the treatment of left main lesions.”
    
      “The EBC represents the finest tradition of collaboration among leaders
      within the European interventional community,” said Shawn McCarthy,
      president and CEO of Tryton Medical. “Tryton is pleased to work with
      these visionaries as we continue a leadership role in pioneering an
      innovative solution to this long-standing challenge in interventional
      cardiology.”
    
      Coronary artery disease often results in the buildup of plaque at the
      site of a bifurcation, where one artery branches from another. Current
      approaches to treating these lesions are time consuming and technically
      difficult. As a result, the side branch is often left unstented, leaving
      it vulnerable to higher rates of restenosis, the re-narrowing of the
      stented vessel following implantation. Bifurcation lesions account for
      as many as one-third of all coronary lesions.1 Left main
      disease, an accumulation of plaque that narrows the base of the coronary
      tree, is a persistent challenge in interventional cardiology, as more
      than 75 percent of left main lesions are bifurcation lesions.
    
About the Tryton Side Branch Stent
      The Tryton Side Branch Stent System is designed to offer a dedicated
      strategy for treating atherosclerotic lesions in the side branch at the
      site of a bifurcation. Tryton’s cobalt chromium stent is deployed in the
      side branch artery using a standard single-wire balloon-expandable stent
      delivery system. A conventional drug-eluting stent is then placed in the
      main vessel.
    
      The stent system has received CE Mark approval in Europe and is
      commercially available in 21 countries throughout Europe and the Middle
      East. It is approved in the United States for investigational use only.
    
      The randomized, controlled Tryton IDE study will compare the use of the
      Tryton stent in the side branch in conjunction with a standard drug
      eluting stent in the main vessel vs. the use of angioplasty in the side
      branch with a standard drug eluting stent in the main vessel for the
      treatment of complex bifurcation disease. The primary endpoint of the
      study is target vessel failure at nine months. A secondary endpoint is
      percent diameter stenosis at nine months in the side branch vessel as
      assessed in an angiographic subgroup.
    
About Tryton Medical, Inc.
      Tryton Medical, Inc., located in Durham, N.C., is a leading developer of
      novel stent systems for the treatment of bifurcation lesions. The
      company was founded in 2003 by Aaron V. Kaplan, M.D. (professor of
      medicine at Dartmouth Medical School/Dartmouth- Hitchcock Medical
      Center) and Dan Cole to develop stents for the definitive treatment of
      bifurcation lesions. The Tryton Side Branch Stent System, approved for
      sale in Europe, is designed to offer a dedicated strategy for treating
      these challenging cases. Privately held, Tryton is backed by Arnerich
      Massena & Associates, Spray Ventures, PTV Sciences, and RiverVest
      Ventures. For more information please visit trytonmedical.com.
    
      1 Scot Garg, et al. EuroIntervention 2011:6: 928-935.
      Available online at http://www.pcronline.com/eurointervention/34th_issue/162/
    
       Tryton Medical, Inc.
Nicole Osmer, 650-454-0504
nicole@nicoleosmer.com     
