TAXUS(R) stent demonstrates excellent efficacy and safety in independent "STENT" registry
25 Oktober 2005 - 11:29PM
PR Newswire (US)
Trends favor Boston Scientific's TAXUS stent over J&J's Cypher
in interim nine-month data from largest independent DES registry in
U.S. VANCOUVER, Oct. 25 /PRNewswire-FirstCall/ -- Angiotech
Pharmaceuticals, Inc. (NASDAQ:ANPINASDAQ:TSX:NASDAQ:ANP) corporate
partner, Boston Scientific ("BSC"), today welcomed interim results
from the independent, multicenter STENT registry that further
demonstrate the efficacy and safety of Boston Scientific's TAXUS(R)
Express(2)(TM) paclitaxel-eluting coronary stent system among
real-world patients with blocked coronary arteries. An analysis of
data on patients who have completed nine months of follow-up to
date revealed a numerical trend favoring the TAXUS stent over
Johnson & Johnson's Cypher(R) sirolimus-eluting stent system in
reducing major adverse cardiovascular events (MACE) and target
vessel revascularization (TVR). The interim results were presented
at the annual Transcatheter Cardiovascular Therapeutics (TCT)
symposium in Washington, D.C. STENT (Strategic Transcatheter
Evaluation of New Therapies) is the first U.S., multicenter,
prospective registry initiated to evaluate the long-term efficacy
and safety of paclitaxel- and sirolimus-eluting coronary stents
among real-world patients and clinical situations. Charles
Simonton, M.D., is chairman of the executive steering committee for
the STENT group. "The present study shows that TAXUS stents are
being implanted in patients who are slightly older, have higher
lesion risk and somewhat smaller vessels than patients receiving
Cypher stents," said Dr. Simonton. "Based on data collected so far,
paclitaxel- and sirolimus-eluting stents demonstrate similar
efficacy and safety overall at nine months. When you adjust the two
groups to account for the higher complexity level of the TAXUS
stent arm, results favor the TAXUS stent, but without statistically
significant differences between the two stents." Eight coronary
interventional centers across the United States are participating
in the registry, which will enroll more than 8,000 patients, the
largest population in any study of its kind. A total of 3,758
patients receiving either the TAXUS stent (1,476) or the Cypher
stent (2,282) had completed nine months of follow up at the time of
the interim analysis. The majority of baseline characteristics were
similar among the two treatment groups, although TAXUS stent
patients tended to be slightly older with more acute coronary
syndrome, slightly smaller vessel diameters and higher ACC lesion
risk scores. Late clinical outcomes trend numerically in favor of
paclitaxel as compared to sirolimus, including death (2.1 vs. 2.7),
myocardial infarction (1.8 vs. 2.2), TVR (3.4 vs. 4.2), and MACE
(6.8 vs. 7.9). In addition, both the TAXUS and Cypher stents showed
low rates of thrombosis that are consistent with results seen in
bare-metal stents. "In contrast to some of the smaller,
single-center trials conducted in Europe, interim data from STENT
suggest that paclitaxel- and sirolimus-eluting stents are either
equal or show a trend favoring the TAXUS stent," said Hank
Kucheman, President of Boston Scientific's Interventional
Cardiology business. "Most importantly, the results confirm what we
have seen again and again in randomized clinical trials like TAXUS
II, IV and V, and in registries like ARRIVE: the TAXUS Express(2)
stent system performs well in real-world patient populations. We
look forward to seeing the full results next year." Additional data
from STENT are scheduled to be presented at the American College of
Cardiology conference in 2006, with the final analysis slated for
presentation at TCT 2006. BSC acquired worldwide exclusive rights
from Angiotech to use paclitaxel to coat its coronary stent
products and has co-exclusive rights to other vascular and
non-vascular products. Vancouver-based Angiotech Pharmaceuticals,
Inc. is a specialty pharmaceutical company pioneering the
combination of pharmaceutical compounds with medical devices and
biomaterials to both create novel solutions for poorly addressed
disease states and dramatically improve surgical outcomes. To find
out more about Angiotech Pharmaceuticals, Inc.
(NASDAQ:ANPINASDAQ:TSX:NASDAQ:ANP), please visit our website at
http://www.angiotech.com/. Statements contained herein that are not
based on historical or current fact, including without limitation
statements containing the words "anticipates," "believes," "may,"
"continue," "estimate," "expects," and "will" and words of similar
import, constitute "forward-looking statements" within the meaning
of the U.S. Private Securities Litigation Reform Act of 1995. Such
forward-looking statements involve known and unknown risks,
uncertainties and other factors that may cause the actual results,
events or developments to be materially different from any future
results, events or developments expressed or implied by such
forward-looking statements. Such factors include, among others, the
following: general economic and business conditions, both
nationally and in the regions in which the Company operates;
technology changes; competition; changes in business strategy or
development plans; the ability to attract and retain qualified
personnel; existing governmental regulations and changes in, or the
failure to comply with, governmental regulations; liability and
other claims asserted against the Company; and other factors
referenced in the Company's filings with the United States
Securities and Exchange Commission or the Canadian securities
regulators. Given these uncertainties, readers are cautioned not to
place undue reliance on such forward-looking statements. The
Company does not assume the obligation to update any
forward-looking statements. FOR ADDITIONAL INFORMATION
-------------------------- Analysts and Investors: Todd Young, Vice
President, Investor Relations and Communications, Angiotech
Pharmaceuticals, Inc. (604) 221-7676 ext 6933 Analysts: Rui Avelar,
Senior Vice President Medical Affairs and Communications, Angiotech
Pharmaceuticals, Inc. (604) 221-7676 ext 6996 Media: Wendy Carhart,
Waggener Edstrom Bioscience, (503) 443-7354, Email: DATASOURCE:
Angiotech Pharmaceuticals, Inc. CONTACT: Analysts and Investors:
Todd Young, Vice President, Investor Relations and Communications,
Angiotech Pharmaceuticals, Inc., (604) 221-7676 ext 6933; Analysts:
Rui Avelar, Senior Vice President Medical Affairs and
Communications, Angiotech Pharmaceuticals, Inc., (604) 221-7676 ext
6996; Media: Wendy Carhart, Waggener Edstrom Bioscience, (503)
443-7354, Email:
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