PreMD's PREVU(x) LT Cleared For Sale in Europe
18 9월 2006 - 11:00PM
PR Newswire (US)
Submission made to Health Canada, plans for submission to FDA on
track TORONTO, Sept. 18 /PRNewswire-FirstCall/ -- Predictive
medicine company PreMD Inc. (TSX: PMD; Amex: PME) today announced
that it has Conformite Europeene (CE)-marked its PREVU(x) LT Skin
Sterol Test, the company's second product in the PREVU(x) family of
skin sterol tests. The CE-Mark designation signifies that the skin
sterol test complies with the essential requirements of the
European Union In Vitro Medical Devices Directive and allows for it
to be sold in the European Union (EU). The CE-marking in Europe
results in a milestone payment to PreMD from its marketing partner,
McNeil Consumer Healthcare. PREVU(x) LT is a lab-processed format
of the PREVU(x) technology which has been developed for use within
the life insurance industry and diagnostic laboratories. "The
clearance of this new laboratory test format significantly expands
the market potential for PREVU(x)," said Dr. Brent Norton,
President and Chief Executive Officer of PreMD. "The clearance of
the product in the EU represents an important achievement for our
company. Furthermore, this second PREVU(x) product is a key
component of our strategy to address multiple markets with multiple
formats of the technology. Our plan for submission of PREVU(x) LT
to the U.S. Food & Drug Administration (FDA) remains on track
for this year." PREVU(x) LT is CE-marked in Europe as a risk
assessment tool for cardiovascular disease. The Technical File for
this product included clinical data from the recently completed
PREPARE (PREVU(x) Predicts Atherosclerosis Risk and Events) study,
conducted in the life insurance industry with the participation of
selected U.S. life insurers. The product was compared to
traditional risk assessment measures. PreMD has also submitted a
Class II Device licence application to Health Canada's Therapeutic
Products Directorate (TPD) for clearance of PREVU(x) LT. The TPD is
the Canadian federal authority that regulates pharmaceutical drugs
and medical devices for human use. PreMD is currently preparing the
premarket notification or 510(k) for submission to the U.S. Food
and Drug Administration (FDA). About PREVU(x)LT PREVU(x) LT
non-invasively measures the amount of cholesterol (sterol) that has
accumulated in the skin tissues, as opposed to blood, by painlessly
collecting skin cells from the palm of the hand using a specially
designed adhesive strip, which is then sent to a laboratory for
processing. No fasting or other patient preparation is required for
the test. The lead product in this family, PREVU(x) Point of Care
(POC) Skin Sterol Test, is cleared for sale in Canada, the U.S. and
Europe and is currently being marketed by McNeil Consumer
Healthcare. About PreMD PreMD Inc. is a world leader in predictive
medicine, dedicated to developing rapid, non-invasive tests for the
early detection of life-threatening diseases. PreMD's
cardiovascular products, which are branded as PREVU(x) Skin Sterol
Test, are licensed worldwide to McNeil Consumer Healthcare. The
company's cancer tests include ColorectAlert(TM), LungAlert(TM) and
a breast cancer test. PreMD's head office is located in Toronto,
and its research and product development facility is at McMaster
University in Hamilton, Ontario. For further information, please
visit http://www.premdinc.com/. For more information about
PREVU(x), please visit http://www.prevu.com/ or call 1-866-283-8328
(North America) or 00-800-8283-8328 (Europe), or email . This press
release contains forward-looking statements. These statements
involve known and unknown risks and uncertainties, which could
cause the Company's actual results to differ materially from those
in the forward-looking statements. Such risks and uncertainties
include, among others, the successful development or marketing of
the Company's products, the competitiveness of the Company's
products if successfully commercialized, the lack of operating
profit and availability of funds and resources to pursue R&D
projects, the successful and timely completion of clinical studies,
product liability, reliance on third-party manufacturers, the
ability of the Company to take advantage of business opportunities,
uncertainties related to the regulatory process, and general
changes in economic conditions. In addition, while the Company
routinely obtains patents for its products and technology, the
protection offered by the Company's patents and patent applications
may be challenged, invalidated or circumvented by our competitors
and there can be no guarantee of our ability to obtain or maintain
patent protection for our products or product candidates. Investors
should consult the Company's quarterly and annual filings with the
Canadian and U.S. securities commissions for additional information
on risks and uncertainties relating to the forward-looking
statements. Investors are cautioned not to rely on these
forward-looking statements. PreMD is providing this information as
of the date of this press release and does not undertake any
obligation to update any forward-looking statements contained in
this press release as a result of new information, future events or
otherwise. (x) Trademark DATASOURCE: PreMD Inc. CONTACT: Ron
Hosking, Chief Financial Officer, Tel: (416) 222-3449 ext. 34,
Email:
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