Angiotech's corporate partner, Boston Scientific, announces Japanese approval for TAXUS(R) Liberté(R) drug-eluting stent system

    VANCOUVER, Jan. 29 /CNW/ - Angiotech Pharmaceuticals, Inc. (NASDAQ:   ANPI,
TSX: ANP), a global specialty pharmaceutical and medical device company, today
announced that its corporate partner, Boston Scientific Corporation (NYSE:  
BSX), has received approval from the Japanese Ministry of Health, Labor and
Welfare (MHLW) to market its TAXUS(R) Liberté(R) paclitaxel-eluting coronary
stent system. Boston Scientific plans to launch the product in Japan once
reimbursement approval is granted. The TAXUS Liberté was approved by the FDA
in October 2008 and was launched in Europe and several other international
markets in 2005.
    "The TAXUS Liberté stent is the latest advance in drug-eluting stent
technology for Japan," said Donald Baim, M.D., Chief Medical and Scientific
Officer of Boston Scientific. "Its safety and efficacy have been well
demonstrated in multiple clinical studies and years of clinical use."
    "We are pleased to see the approval of TAXUS Liberté in Japan as it
demonstrates our partner's commitment to expanding its international
acceptance," said Dr. William Hunter, President and CEO of Angiotech.
"Japanese patients and their families struggling with coronary artery disease
should soon be able to benefit from this proven technology."
    TAXUS Liberté is the only second-generation drug-eluting stent approved
for use in Japan. The TAXUS Liberté stent will replace the TAXUS
Express(2)(TM) stent, marketed in Japan since May 2007. Significant design
improvements over the first-generation stent include thinner struts and a more
uniform stent geometry.

    Forward-Looking Statements
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we operate; market demand; technological changes that could impact our
existing products or our ability to develop and commercialize future products;
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in pre-clinical and clinical product development processes; adverse findings
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partners; decisions, and the timing of decisions, made by health regulatory
agencies regarding approval of our technology and products; the requirement
for substantial funding to conduct research and development and to expand
manufacturing and commercialization activities or consummate acquisitions; and
any other factors that may affect performance. In addition, our business is
subject to certain operating risks that may cause the actual results expressed
or implied by the forward-looking statements in this press release to differ
materially from our actual results. These operating risks include: our ability
to attract and retain qualified personnel; our ability to successfully
complete pre-clinical and clinical development of our products; changes in
business strategy or development plans; our failure to obtain patent
protection for discoveries; loss of patent protection resulting from third
party challenges to our patents; commercialization limitations imposed by
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asserted against us; our ability to obtain and enforce timely patent and other
intellectual property protection for our technology and products; the ability
to enter into, and to maintain, corporate alliances relating to the
development and commercialization of our technology and products; market
acceptance of our technology and products; our ability to successfully
manufacture, market and sell our products; the continued availability of
capital to finance our activities; and any other factors referenced in our
other filings with the Securities and Exchange Commission ("SEC") and
applicable Canadian regulatory authorities. For a more thorough discussion of
the risks associated with our business, see the "Risk Factors" section in our
annual report for the year ended December 31, 2007 filed with the SEC on Form
40-F and our quarterly report for the three months ended September 30, 2008
filed with the SEC on Form 10-Q.
    Given these uncertainties, assumptions and risk factors, readers are
cautioned not to place undue reliance on such forward-looking statements.
Except as required by law, we disclaim any obligation to update any such
factors or to publicly announce the result of any revisions to any of the
forward-looking statements contained in this press release to reflect future
results, events or developments.

    (C) 2009 Angiotech Pharmaceuticals, Inc. All Rights Reserved.

    Boston Scientific Corporation acquired worldwide exclusive rights from
Angiotech to use paclitaxel to coat its coronary stent products and has
co-exclusive rights to certain peripheral vascular and non-vascular products.

    TAXUS(R) Liberté and Express(2)(TM) are registered trademarks of Boston
    Scientific Corporation.

    About Angiotech Pharmaceuticals

    Angiotech Pharmaceuticals, Inc. is a global specialty pharmaceutical and
medical device company with over 1,500 dedicated employees. Angiotech
discovers, develops and markets innovative treatment solutions for diseases or
complications associated with medical device implants, surgical interventions
and acute injury. To find out more about Angiotech (NASDAQ:   ANPI, TSX: ANP),
please visit our website at

For further information:

For further information: DeDe Sheel, Investor Relations and Corporate
Communications, Angiotech Pharmaceuticals, Inc., (415) 293-4412,

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