Direct Flow Medical Strengthens SALUS Pivotal Trial

SANTA ROSA, Calif.– April 28, 2016 – Direct Flow Medical, Inc., a medical device company developing and commercializing transcatheter heart valve therapy products to treat structural heart disease, today announced modifications to its U.S. SALUS pivotal trial to include best practices and clinical comparison with all currently available U.S. TAVR devices.

The Direct Flow Medical transcatheter aortic valve system, with more than 2,500 implants and excellent published clinical results including low rates of paravalvular leak, pacemaker implant, and mortality, is the only non-metallic, conformable transcatheter aortic valve that can be functionally assessed, repositioned, and retrieved prior to final implant.

The SALUS pivotal trial was initiated June 2015 with target enrollment of 1,262 subjects at up to 45 U.S. investigational sites to evaluate the Direct Flow Medical TAVR System with one TAVR device.  Based on recent FDA approvals,the trial now features improved screening, enhanced options for anesthesia, optional intraprocedural dilatation, use of the new DirecTrack delivery system, comparison with all current commercially-available U.S. TAVR devices and a new target enrollment of 648 subjects.

“Utilizing best practices, comparing with all TAVR devices and being able to evaluate a new delivery system places the SALUS Trial at the leading edge of TAVR science,” stated Scott Lim, M.D., University of Virginia, and SALUS trial co-principal investigator.  “These changes elevate SALUS trial value and meaningfully evaluate product performance relative to available TAVR technology,” echoed Isaac George, M.D. Columbia University, and SALUS trial co-principal investigator.

Dan Lemaitre, President and CEO stated, “The strengthened SALUS trial design reflects our agility in a dynamic global TAVR market to provide the scientific community with a truly meaningful investigation and enhances our ability to achieve our year-end enrollment target.”

 

About Direct Flow Medical, Inc.

Direct Flow Medical, Inc.is a privately-held medical device company developing and commercializing novel transcatheter heart valve therapy products to treat structural heart disease.

The company sponsors the SALUS Pivotal Trial in the U.S.to investigate the Direct Flow Medical Transcatheter Aortic Valve System for treating high and extreme risk severe symptomatic aortic stenosis.  The system is commercially available in Europe for treating extreme surgical risk aortic stenosis.

Company website:  directflowmedical.com

 

Media contact:

Brian McIntee
Direct Flow Medical, Inc.
bmcintee@directflowmedical.com
+1 (707) 576-0420

 

Direct Flow Medical, DirecTrack, and the Direct Flow logo are trademarks of Direct Flow Medical, Inc.

 

The information on this site is only intended for health care providers in certain markets outside the United States (US) where the Direct Flow Medical Trancatheter Aortic Valve Replacement System is approved for use as indicated by the instructions for use. The information on this page is not intended for health care providers in the US or US health care institutions as this site contains information about a product that is limited by US law to investigational use.

I am a health care
provider in the
United States
I am a health care
provider outside
the United States