2014

XTENT Announces European Regulatory Update

    MENLO PARK, Calif., June 12 /PRNewswire-FirstCall/ -- XTENT, Inc.
 (Nasdaq:   XTNT) today announced a progress update regarding its application
 to the designated European Notified Body for CE Mark approval of its Custom
 NX(R) DES System. XTENT's European Notified Body confirmed that recently
 presented six-month follow up results from the CUSTOM III study will be
 incorporated by the Drug Agency, which reviews the drug formulation
 submission of XTENT's CE Mark application, into its current review cycle.
 XTENT's CE Mark application, which included two components, the XTENT
 design dossier and the drug formulation submission, was filed in December
 2007.
 
     "Given the positive results of CUSTOM III, we are encouraged that the
 Drug Agency, which has already approved Biolimus A9(R) and PLA combinations
 on two other DES platforms, has accepted the additional data for review.
 This, we believe strengthens an already robust submission for our Custom NX
 System," said Gregory D. Casciaro, XTENT's President and CEO. The company
 anticipates a response from its European Notified Body regarding its CE
 Mark application this summer.
 
     About the Custom NX(R) DES System
 
     Custom NX is designed to enable a more personalized approach to the
 treatment of arterial disease based on each patient's individual lesion
 characteristics. The Custom NX system allows physicians to customize the
 length and diameter of the stent at the site of the lesion. The system
 features a proprietary modular stent design that consists of multiple 6 mm
 cobalt chromium segments coated with Biolimus A9(R) and PLA, a
 biodegradable drug carrier. The Custom NX delivery system enables the stent
 length to be adjusted in 6mm increments and allows for the placement of up
 to 60mm of stent at one or more locations. The Custom NX DES System has not
 been approved for sale by any regulatory authority.
 
     About XTENT
 
     XTENT, Inc. is a medical device company focused on developing and
 commercializing innovative customizable drug eluting stent (DES) systems
 for the treatment of coronary artery disease (CAD). CAD is the most common
 form of cardiovascular disease and the number one cause of death in the
 United States and Europe. XTENT(R) Custom NX(R) DES Systems are designed to
 enable the treatment of single lesions, long lesions and multiple lesions
 of varying lengths and diameters, in one or more arteries with a single
 device.
 
     Forward Looking Statements
 
     This press release contains forward-looking statements within the
 meaning of the U.S. Private Securities Litigation Reform Act of 1995.
 Statements in this press release regarding XTENT's business that are not
 historical facts may be "forward-looking statements" that involve risks and
 uncertainties. Specifically, these statements include, but are not limited
 to those concerning: XTENT's expectations with respect to the timing or
 results of its regulatory filings, the timing of responses to its
 regulatory filings and the timing of the commercialization of its products.
 Forward-looking statements are based on management's current, preliminary
 expectations, and are subject to risks and uncertainties that could cause
 actual results to differ from the results predicted and which are included
 in the "Risk Factors" section of XTENT's quarterly report on Form 10-Q for
 the quarter ended March 31, 2008. This quarterly report was filed with the
 SEC on May 13, 2008, and is available on the company's investor relations
 website at http://www.xtentinc.com and on the SEC's website at
 http://www.sec.gov. Undue reliance should not be placed on forward-looking
 statements, which speak only as of the date they are made. XTENT undertakes
 no obligation to update publicly any forward-looking statements to reflect
 new information, events or circumstances after the date they were made, or
 to reflect the occurrence of unanticipated events
 
 
 

SOURCE XTENT, Inc.

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