Theresa Catharina de Góes Campos

  De: PR Newswire Brasil
Para: THERESA CATHARINA DE GÓES CAMPOS
Assunto: TAXUS(R) Liberte(TM) Stent System Receives European Approval for Three Complex Coronary Procedures
TAXUS(R) Liberte(TM) Stent System Receives European Approval for Three Complex Coronary Procedures
16 de maio de 2006 09:00 HORALOCAL


TAXUS(R) Liberte(TM) Stent System Receives European Approval for
Three Complex Coronary Procedures

Boston Scientific's Second-Generation Stent System Now Approved for
Treatment of Acute Mycocardial Infarction, Total Occlusions and
In-Stent Restenosis

Large Vessel TAXUS Liberte Stent Also Receives CE Mark

NATICK, Mass., and PARIS, May 16 /PRNewswire/ -- Boston Scientific
Corporation (NYSE: BSX) announced today that it has received
indication extensions to the European CE mark for its TAXUS(R)
Liberte(TM) paclitaxel-eluting coronary stent system for use in some
of the most challenging coronary procedures.
The new labeling reflects a review of TAXUS clinical data by the
European regulatory agency. In addition to its existing indication
for the treatment of de-novo lesions in native coronary arteries, the
TAXUS Liberte stent system is now indicated in Europe for the
treatment of restenotic lesions (in-stent restenosis, or ISR) and
total occlusions (TO) in patients with coronary artery disease,
including acute myocardial infarction (AMI). These three new
indications account for more than 20 percent of all coronary
interventions.
The TAXUS Liberte stent system is now the only drug-eluting stent
system with these new indications for use in Europe.
This revised labeling follows the excellent clinical outcomes the
TAXUS stent system has shown in the treatment of complex lesions in
recent clinical trials and registries, including the TAXUS V ISR
trial and the MILESTONE II, WISDOM, ARRIVE, and OLYMPIA registries.
In addition to the three new indications, the large vessel diameter
TAXUS Liberte stent also received the CE mark. This stent uses a
modified cell design intended for drug delivery in larger vessels,
and will be available in a 4.0 mm diameter and seven different
lengths.
"The European approval for new indications recognizes the
strong long-term performance of the TAXUS stent system across complex
patients and lesions," said Jeff Goodman, President of Boston
Scientific International. "It allows physicians to treat difficult
cases of coronary artery disease with the most advanced technology."

Boston Scientific is a worldwide developer, manufacturer and marketer
of medical devices whose products are used in a broad range of
interventional medical specialties. For more information, please
visit: www.bostonscientific.com.

This press release contains forward-looking statements. Boston
Scientific wishes to caution the reader of this press release that
actual results may differ from those discussed in the forward-looking
statements and may be adversely affected by, among other things,
risks associated with new product development and commercialization,
clinical trials, intellectual property, regulatory approvals,
competitive offerings, integration of acquired companies, Boston
Scientific's overall business strategy, and other factors described
in Boston Scientific's filings with the Securities and Exchange
Commission.

SOURCE Boston Scientific Corporation
05/16/2006
CONTACT: Geraldine Varoqui, Boston Scientific PR Manager
International, Tel: +49-2102-489-461, varoquig@bsci.com; or Maren
Koban, BSC press office, Tel: +44-20-7973-4497,
mkoban@hillandknowlton.com
Web site: http://www.bostonscientific.com
(BSX)


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