Two-year data for Angiotech's Vascular Wrap(TM) Paclitaxel-Eluting Mesh to be presented at European vascular symposium

    STRASBOURG, France and VANCOUVER, April 26 /CNW/ - Angiotech
Pharmaceuticals, Inc. (NASDAQ:   ANPI, TSX: ANP), a global specialty
pharmaceutical and medical device company, announced that the two-year data
from its European pivotal trial examining the Vascular Wrap(TM)
Paclitaxel-Eluting Mesh ("Vascular Wrap(TM)") will be presented today at a
scientific forum in Europe. The two-year study examined the safety and
efficacy of the Vascular Wrap(TM) for use in arterial bypass surgery in
patients with peripheral arterial disease (PAD). Dr. Lajos Matyas is
presenting the results at the 2007 European Symposium of Vascular Biomaterials
(ESVB) in Strasbourg, France.
    "We are pleased to have this opportunity to present these encouraging
results from our two-year European Vascular Wrap(TM) study to the physicians,
researchers and other healthcare professionals at ESVB," said Dr. Rui Avelar,
Chief Medical Officer at Angiotech.
    "The results of this 109-patient study suggest that the Vascular Wrap(TM)
combined with an ePTFE graft may be a promising future therapy option for
patients with PAD who require arterial bypass surgery," said Dr. Lajos Matyas,
a lead investigator based in Miskolc, Hungary, who enrolled the highest number
of patients out of the nine clinical centres in Europe involved in the study.
    Angiotech initially released the results from the two-year Vascular
Wrap(TM) study in November 2006. The objectives of this two-year study were to
assess the safety and clinical performance of the Vascular Wrap(TM) in
combination with an ePTFE vascular graft following surgery to treat patients
suffering from advanced peripheral arterial disease in their lower limbs. The
Vascular Wrap(TM) in combination with an ePTFE graft was compared to a control
group of patients that received standard of care - an ePTFE graft alone. Some
of the highlights of the two-year study that will be presented at ESVB

    -   Statistically significant difference in a key efficacy measurement:

        -  The development of neointimal hyperplasia, which is a common
           complication of bypass surgery involving a thickening of the
           inner layer of the blood vessel, can ultimately result in the
           closing of the newly opened or grafted blood vessel and lead to
           limb amputation.
        -  When comparing the treatment arm relative to the control, the
           Vascular Wrap(TM) maintained the mean diameter of the distal
           anastomosis during the 24-month trial compared to a decrease in
           mean diameter in the control arm. This reached statistical
           significance at two years (p=0.03). A decrease in mean
           diameter of distal anastomosis in the control arm indicates the
           development of neointimal hyperplasia.

    -   The Vascular Wrap(TM) trial produced evidence of improved patient

        -  The trial produced evidence that the Vascular Wrap(TM) reduced the
           overall incidence of amputation and prolonged limb retention time.
           The control group had an almost 19% higher probability of losing
           their limb compared to the treatment arm.
        -  The treated group had an overall lower incidence of amputations
           (15.5%, 11/71 subjects) compared to the control group (18.4%,
           7/38 subjects).
        -  While the sample size was small, diabetic subjects appeared to
           experience benefits from the Vascular Wrap, which was associated
           with a 41.3% reduction in the incidence of amputations. The
           treated group of diabetic subjects had a lower incidence of
           amputations (13.8%, 4/29 diabetic subjects) compared to the
           control group (23.5%, 4/17 diabetic subjects).

    -   The trial results produced evidence that the Vascular Wrap(TM) is
        well tolerated:

        -  Adverse events (AE) leading to death occurred in a lower
           percentage of treated subjects (11%, 8/71 subjects), than in
           controls (18%, 7/38 subjects).
        -  The incidences of adverse events and serious adverse events were
           comparable in treated (graft with Vascular Wrap) and control
           (graft alone) groups.
        -  No adverse events were considered by the investigators to be
           related to the use of the Vascular Wrap.
        -  Overall, the action taken to resolve AEs was similar for the two
           groups, and the outcomes were comparable.

    About the Study

    This single-blind study enrolled a total of 109 patients at nine clinical
centres in Europe as well as the Dutch Antilles and randomized patients with
peripheral vascular disease in a 2:1 fashion. The treatment arm enrolled
patients with a synthetic bypass graft plus the Vascular Wrap(TM)
paclitaxel-eluting mesh and the control arm enrolled patients with a synthetic
bypass graft alone.

    About peripheral arterial disease (PAD)

    Peripheral vascular disease, especially peripheral arterial disease (PAD)
is a prevalent cause of morbidity and mortality among the aging population
worldwide. Artery stenosis or occlusion causes reduced blood flow, decreased
mobility, and limb loss in the later disease stages. Population surveys in
Europe and the U.S. estimate that PAD prevails in 10-25% of the population;
most surveys give a prevalence of 20% for lower extremity PAD in the overall
population. The major cause of PAD is atherosclerosis, in which deposits
narrow and eventually occlude the arteries. The disease progresses in the
lower extremities to critical limb ischemia (CLI), characterized by leg pain
at rest, skin ulceration, gangrene, and ultimately amputation. Among patients
diagnosed with CLI, 25% may require amputation within a year.
    Limb salvage depends on restoring and maintaining blood flow in the CLI
patient. Surgical interventions include endovascular therapy (angioplasty and
stenting). However, in patients with severe occlusion and stenosis, small
vessel occlusion, calcified lesions, as well as those with diabetes, surgical
bypass provides a final option to manage the occlusion(s) prior to amputation.
The success of grafting to restore blood flow depends on inflow and outflow of
the graft. The trial results show trends that suggest that the use of the
Vascular Wrap(TM) in these procedures may increase the success rates of
vascular graft surgery.

    Vascular Wrap(TM) Paclitaxel-Eluting Mesh/ePTFE Graft Combination

    Angiotech's Vascular Wrap(TM) paclitaxel-eluting mesh/ePTFE graft
combination product technology is designed to and in development for use in
hemodialysis access and peripheral arterial bypass surgery. It is a
combination product consisting of both the ePTFE graft and the Vascular
Wrap(TM) paclitaxel-eluting mesh. The Vascular Wrap(TM) component is a
biodegradable mesh implant incorporating Angiotech's paclitaxel technology in
a novel biomaterial with the goal of mitigating scar formation caused by
abnormal blood flow thereby potentially enhancing graft patency rates in
AV-access patients as well as in peripheral bypass procedures.

    Note on Forward Looking Statements:

    Statements contained in this press release that are not based on
historical fact, including without limitation statements containing the words
"believes," "may," "could", "plans," "will," "estimate," "continue,"
"anticipates," "intends," "expects" and similar expressions, constitute
"forward-looking statements" within the meaning of the U.S. Private Securities
Litigation Reform Act of 1995 and constitute "forward-looking information"
within the meaning of applicable Canadian securities laws. All such statements
are made pursuant to the "safe harbor" provisions of applicable securities
legislation. Forward-looking statements may involve, but are not limited to,
comments with respect to our objectives and priorities for 2006 and beyond,
our strategies or future actions, our targets, expectations for our financial
condition and the results of, or outlook for, our operations, research
development and further product and drug development. Such forward-looking
statements also 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 are taken into
account as part of our assumptions underlying these forward-looking statements
and include, among others, the following: general economic and business
conditions, both nationally and in the regions in which we operate;
technological changes that impact our existing products or our ability to
develop and commercialize future products; 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; adverse results or unexpected delays in
drug discovery and clinical development processes; failure to obtain patent
protection for discoveries; loss of patent protection resulting from third
party challenges to our patents; commercialization limitations imposed by
patents owned or controlled by third parties; dependence upon, and
relationships with strategic alliance partners to develop and commercialize
products and services based on our work; our ability to obtain rights to
technology from licensors; liability for patent claims and other claims
asserted against us; the requirement for substantial funding to conduct
research and development and to expand commercialization activities or
consummate acquisitions; the size of the market and the potential market for
our products in specific disease areas, including peripheral arterial disease,
other factors referenced in our annual information form and other filings with
the applicable Canadian securities regulatory authorities or the Securities
and Exchange Commission; 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 report to differ materially from our actual results. These
operating risks include: our ability to successfully complete preclinical and
clinical development of our products; the ability to obtain and enforce timely
patent and other intellectual property protection for our technology and
products; decisions, and the timing of decisions, made by health regulatory
agencies regarding approval of our technology and products; the ability to
complete and maintain corporate alliances relating to the development and
commercialization of our technology and products; market acceptance of our
technology and products; the competitive environment and impact of
technological change; the continued availability of capital to finance our
activities; our ability to integrate into our business the operations of AMI;
and, our ability to achieve the operational and other synergies and the other
commercial or financial benefits expected as a result of the acquisition of
    Given these uncertainties, assumptions and risk factors, readers are
cautioned not to place undue reliance on such forward-looking statements. 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 report to reflect future results, events or developments.

    Vascular Wrap(TM) is a trademark of Angiotech Pharmaceuticals, Inc.
    (C) 2007 Angiotech Pharmaceuticals, Inc. All rights reserved.

For further information:

For further information: Janet Craig, VP, Investor Relations and
Corporate Communications, Angiotech Pharmaceuticals, Inc., (604) 221-6933,; Jodi Regts, Manager, Corporate Communications, Angiotech
Pharmaceuticals, Inc., (604) 221-7930,

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