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For the First Time, at EuroPCR, InspireMD Will Provide a Sneak Preview of the Next Generation MGuard Prime(R), a State of the Art Net Protective Cobalt Chromium Stent System
Date:5/26/2010

of the INSPIRE trial, and long awaited 1 year clinical FU with 6 month angiographic results.

The INSPIRE Trial from Sao-Paulo, Brazil is a 30 patients' study that enrolled SVG and native coronary patients. Acute results as well as interim results have previously been presented by Dr. A. Abizaid, the study's primary investigator.

The international iMOS registry has crossed the 200 patients' milestone. The registry will enroll 1000 'real world' MGuard(TM) patients in Europe, Asia and South America. Data from the registry, an unselected heterogeneous population, will be used to support data from other clinical studies. Interim data analysis will be presented by Prof. GB. Danzi, from the iMOS steering committee, at InspireMD's evening symposium this evening.

About MGuard(TM) Coronary

MGuard(TM) presents a novel combination of a coronary stent merged with an embolic protection. The embolic protection is comprised of an ultra-thin polymer mesh sleeve that wraps the stent. The protective sleeve is composed of a micron-level-fiber which is knit in order to ensure flexibility while retaining the strength characteristics of the fiber material. The sleeve is designed to expand seamlessly when the stent is deployed, without affecting the structural integrity of the stent. The MGuard(TM) coronary stent provides permanent embolic protection, without complicating deliverability. Reduced injury to the vessel as a result of diffused stent pressure is a benefit of the sleeve which may lead to lower risk of restenosis. MGuard(TM) is CE Mark approved.

The MGuard(TM) Coronary's innovative concept has enjoyed an enthusiastic welcome from leading
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SOURCE InspireMD
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