SAN RAMON, Calif., Oct. 27, 2017 /PRNewswire/ -- BioVentrix, Inc. a pioneer of technologies and procedures for less invasive treatment of heart failure (HF), today announced that the Revivent TC™ TransCatheter Ventricular Enhancement System will be featured during the presentation of a Revivent TC procedure at the 29th Transcatheter Cardiovascular Therapeutics (TCT), in Denver, Colorado. Prof. Andrew Wechsler, cardiothoracic surgeon, will present the procedure on Monday, October 30th.
Other BioVentrix events at TCT include the presentation of long-term clinical outcomes by Prof. Christoph Schmitz, Ludwig Maximilian University, Munich, Germany on Monday, October 30th. Additionally, Dr. Patrick Klein will present the preliminary clinical outcomes at the St. Antonius Hospital in Nieuwegein, Netherlands on Wednesday, November 1st.
"BioVentrix continues to gain adoption with the Revivent TC system for treating post-MI, ischemic cardiomyopathy patients. We have commercialized the system in Europe and Asia. Over the past few months we have commenced patient enrollment in the FDA-approved ALIVE pivotal clinical trial. The BioVentrix presentations at TCT offer a comprehensive view of the LIVE™ procedure and the positive short- and long-term clinical outcomes of the Revivent TC system," said Mr. Kenneth Miller, President and CEO of BioVentrix, Inc.
TCT PRESENTATION SCHEDULE (listed chronologically)
Monday, October 30th
Wednesday, November 1st
All presentations are listed in Mountain Daylight Time and will take place at the Colorado Convention Center.
About BioVentrix and the Revivent TC System
BioVentrix, a privately held medical technology company headquartered in San Ramon, Calif., is focused on developing and commercializing minimally invasive therapies for treating HF. The company has received CE mark certification for the Revivent TC TransCatheter Ventricular Enhancement System: a hybrid closed-chest procedure to treat patients suffering from heart failure symptoms related to cardiomyopathy. BioVentrix is currently enrolling patients in the ALIVE pivotal clinical trial. The trial is designed to demonstrate the safety and effectiveness of the Revivent TC™ TransCatheter Ventricular Enhancement System. The ALIVE trial plans to enroll 120 patients at up to 20 sites in the U.S. and U.K. with a primary endpoint analysis at 1 year. Placement of the Revivent TC System via the LIVE procedure obviates the need for more invasive surgery. Instead, small titanium anchors are placed along the outer surface of the heart and along one of the interior walls via a catheter-based approach. The anchors are then pulled towards one another, effectively excluding the scarred and non-functioning heart wall. Ventricular volume is immediately reduced as a result of the exclusion, by as much as 30-40 percent1.
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Note: The Revivent TC System is approved for sale in Europe; it is not approved for sale in the United States.
1Wechsler, A. et al., Clinical benefits twelve months after less invasive ventricular restoration operations without ventriculotomy. Annual meeting of the European Society of Cardio-Thoracic Surgery, 07 Oct. 2013, Vienna, Austria.
SOURCE BioVentrix, Inc.