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InspireMD's MGuard Embolic Protection Stent (EPS) Shows Lower Mortality Rate in STEMI Patients at Six Months Compared to Control Group
Date:5/23/2013

rotection stent, as MGuard EPS outperformed drug-eluting and bare metal stents in complete ST-segment resolution," said Professor Dr. Sigmund Silber , Director of the Heart Center at the Isar Academic Teaching Site of the University of Munich. "The six-month MASTER results highlight the enduring benefits of the MGuard EPS, with a consistent trend in lower mortality."

In the MASTER trial, a total of 433 patients with STEMI presenting within 12 hours of symptom onset undergoing percutaneous coronary intervention were randomized at 50 sites in 9 countries to the MGuard EPS (n = 217) or commercially available bare metal or drug-eluting stents (n = 216).

"The body of positive clinical evidence supporting the use of the MGuardEPS continues to grow," said Alan Milinazzo , President and Chief Executive Officer of InspireMD. "Both the 6-month data and the subgroup analysis presented this week at EuroPCR in Paris, suggest that our technology offers improved embolic protection over the current generation of bare metal and drug eluting stents for the STEMI patient. Advancing embolic protection without requiring physicians to increase procedure time or dramatically change their technique is a major benefit of the MGuard EPS."

Watch the video: https://www.youtube.com/watch?v=EbrhcQMM7YE

Conference Call and Webcast Details

InspireMD will host a conference call and webcast to review 6-month MASTER trial data on Thursday May 23, 2013 at 8:00 ET, 14:00 CET.  To access the call, participants should dial the following numbers:

  • U.S. and Canada:  +1-888-417-8516
  • Paris:            +33-08-00-90-26-40
  • International:   &
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SOURCE InspireMD, Inc.
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