Mexican Department of Public Health to Launch S...
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QIAGEN's digene HPV Test Selected for World's First National
HPV Screening Program
Mexico City, Mexico - Nov. 19, 2008 - In a campaign to significantly
reduce the most common cancer affecting Mexican women, the Mexican
Public Health Agency (Secretaria de Salud or SSA) has announced it is
launching the first phase of a program that will offer testing for
human papillomavirus (HPV), the primary cause of cervical cancer, to
low-income women age 35-65. The cost of the testing will be covered
by the agency. In the first phase of the screening program, which is
beginning this month, more than 200,000 women in the lowest-income
125 counties are being offered the papillomavirus test along with the
traditional Pap smear. In 2009, the pilot program will be expanded to
include another 600,000 women in the 20 states with the highest death
rate from cervical cancer.
Since taking office, President Felipe Calderon has made reducing
health inequalities in Mexico a top priority for his administration.
Cervical cancer is a major focus of this campaign, since so many
Mexican women are affected - more than 12,000 a year. One of the
national initiatives to date has been coordination among the social,
private and public sectors to increase the efficiency and efficacy of
cervical cancer prevention by modifying the Official Mexican Norm
(NOM-014-SSA2-1994) for the disease. The changes are designed to
better facilitate the prevention, diagnosis and treatment of cervical
cancer among the most vulnerable women through public education and
use of the most advanced, effective technologies for screening -
including the HPV test.
Infection with the papillomavirus is very common. In fact, the World
Health Organization estimates that 11 percent of Mexican women carry
cervical HPV at any given time.
"As in many countries, cervical cancer is the most prevalent cancer
in Mexican women between the ages of 15-44. Every year, more than
12,000 Mexican women are diagnosed with cervical cancer and nearly
half of them die. Yet this is an entirely preventable disease," said
Peer Schatz, CEO of QIAGEN (Nasdaq: QGEN; Frankfurt, Prime Standard:
QIA), the company that developed the digene® HPV Test, which will be
used in the SSA's program and is the only such test approved by the
U.S. Food and Drug Administration. It also is available in many other
countries of the world. "The Mexican government is taking a
leadership role in Latin America, and the world, and QIAGEN is
committed to joining with the SSA to assure that our advanced
screening technology is accessible to women everywhere, no matter
what their income level or social class."
In the majority of women, the virus goes away or is suppressed by the
body before it causes any problems. However, in others, the infection
lingers and can cause abnormal cells to form. While the traditional
Pap smear is usually able to find abnormal cells, it sometimes misses
them. A study published in the Journal of the National Cancer
Institute found that about one-third of invasive cervical cancers
developed in women whose smears had appeared normal. In contrast, HPV
testing detects the presence of the virus itself. In the national
norms for cervical cancer prevention, which were updated in 2007,
physicians are advised that they can supplement the Pap with HPV
testing in women 25-65 for additional protection. If abnormal cells
are diagnosed early, they can be removed before they develop into
cervical cancer.
It is estimated that 6 million women a year will be eligible for HPV
testing through the Mexican public health system once the screening
program is national. An additional 1 million women can access the
test using private insurance.
About HPV and cervical cancer (theHPVtest.com and
theHPVtest.com/espanol)
Worldwide, cervical cancer affects nearly 500,000 women annually and,
after breast cancer, is the second-most-common malignancy found in
women. Cervical cancer is caused by "high-risk" types of the human
papillomavirus (HPV). It's estimated that 80 percent of women will
get an HPV infection at some point in their lives. However, in most
cases, the infection goes away or is suppressed by the body without
causing problems. It is only infections that persist that can cause
abnormal cells to form that may develop into cervical cancer if not
detected and treated early. In Mexico, current estimates from the
World Health Organization indicate that 12,516 women are diagnosed
with cervical cancer every year, and 5,777 die from the disease.
About QIAGEN (qiagen.com)
QIAGEN N.V., a Netherlands holding company, is the
leading global provider of sample and assay technologies. Sample
technologies are used to isolate and process DNA, RNA and proteins
from biological samples such as blood or tissue. Assay technologies
are used to make such isolated biomolecules visible. QIAGEN has
developed and markets more than 500 sample and assay products as well
as automated solutions for such consumables. The company provides its
products to molecular diagnostics laboratories, academic researchers,
pharmaceutical and biotechnology companies, and applied
testing customers for purposes such as forensics, animal or food
testing and pharmaceutical process control. QIAGEN's assay
technologies include one of the broadest panels of molecular
diagnostic tests available worldwide. This panel includes the only
FDA-approved test for human papillomavirus (HPV), the primary cause
of cervical cancer. QIAGEN employs more than 2,900 people in over 30
locations worldwide.
Certain of the statements contained in this news release may be
considered forward-looking statements within the meaning of Section
27A of the U.S. Securities Act of 1933, as amended, and Section 21E
of the U.S. Securities Exchange Act of 1934, as amended. To the
extent that any of the statements contained herein relating to
QIAGEN's products, markets, strategy or operating results are
forward-looking, such statements are based on current expectations
that involve a number of uncertainties and risks. Such uncertainties
and risks include, but are not limited to, risks associated with
management of growth and international operations (including the
effects of currency fluctuations and risks of dependency on
logistics), variability of operating results, the commercial
development of the applied testing markets, clinical research markets
and proteomics markets, women's health/HPV testing markets, nucleic
acid-based molecular diagnostics market, and genetic vaccination and
gene therapy markets, changing relationships with customers,
suppliers and strategic partners, competition, rapid or unexpected
changes in technologies, fluctuations in demand for QIAGEN's products
(including fluctuations due to general economic conditions, the level
and timing of customers' funding, budgets, and other factors), our
ability to obtain regulatory approval of our infectious disease
panels, difficulties in successfully adapting QIAGEN's products to
integrated solutions and producing such products, the ability of
QIAGEN to identify and develop new products and to differentiate its
products from competitors' products, market acceptance of QIAGEN's
new products and the integration of acquired technologies and
businesses. For further information, refer to the discussions in
reports that QIAGEN has filed with, or furnished to, the U.S.
Securities and Exchange Commission (SEC).
Investor Relations Media Relations
Dr. Solveigh Mähler Dr. Thomas Theuringer
Director Investor Relations Associate Director Public
QIAGEN N.V. Relations
+49 2103 29 11710 QIAGEN GmbH
e-mail: +49-2103-29-11826
solveigh.maehler@qiagen.com email:
thomas.theuringer@qiagen.com
Albert F. Fleury
Director Corporate Finance and Myriam Maldonado Tapia - Gricorp
Investor Relations North America Ketchum
QIAGEN Gaithersburg, Inc. 52.45.88.55. ext. 202 (Mexico)
+1 301 944 7028 myriam.maldonado@ketchum.com
e-mail: albert.fleury@qiagen.com
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