- The careHPV™ Test
is the first HPV diagnostic designed for regions with limited healthcare
infrastructure, complementing QIAGEN's market-leading digene HC2
HPV Test
- Commercial launch of careHPV Test in India
enables high-quality screening for prevention of cervical
cancer among women in low-resource areas
- The careHPV
Test plays an important role in QIAGEN's Corporate Social Responsibility
effort around the world, especially in low-resource areas
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QIAGEN N.V. today announced the commercial launch in India of its careHPV™ Test, the
only molecular diagnostic for high-risk human papillomavirus (HPV)
designed to screen women in settings with limited healthcare infrastructure,
such as areas lacking electricity, water or laboratories. HPV is the primary
cause of cervical
cancer in women,
so screening for the viral infection is a powerful strategy for prevention and
early treatment of the deadly cancer. ThecareHPV Test was launched
commercially in China in 2013 and has been used in several other countries,
including as part of QIAGEN's corporate
social responsibility effort,
QIAGENcares.
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The careHPV
Test for low-resource settings is highly complementary with QIAGEN's digene HC2 HPV Test, the world's most
validated and sensitive diagnostic
test for
detection of high-risk HPV. The digene HC2 HPV Test is recognized as the "gold
standard" in HPV screening and is widely used in developed countries
and in large cities in emerging
markets.
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About 72,000 women in
India die of
cervical cancer each year, more than one-fourth of the world's 270,000 annual
deaths. In India, cervical cancer accounts for about 20% of all cancer-related
deaths in women and is the number one cause of death in middle-aged Indian
women.
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"The launch of careHPV
in India will help in efforts to reduce the high burden of cervical cancer for
women in India," said Dr. Victor Shi, President of QIAGEN Asia
Pacific. "With the digene HC2 HPV Test serving areas that have modern
healthcare infrastructure
and the careHPV Test
serving low-resource areas, QIAGEN is expanding our role as the global leader in preventive
screening for
cervical cancer and continuing to contribute to women's health around the
world."
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Dr. Partha Basu, Head of the Department of Gynecological
Oncology and
Officer In Charge, Division of Preventive Oncology, Chittaranjan National
Cancer Institute, noted the importance
of the two-tiered approach to screening: "Based on the findings of the
screening project that we have been doing for four years in Kolkata and
surrounding areas, there is a need for a cost-effective and easy-to-use test
which can best meet the requirements of low-resource settings. Availability of
thecareHPV Test is an important step forward for the prevention of
cervical cancer in India."
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QIAGEN's robust, portable and easy-to-use careHPV Test combines the power
of advanced molecular technologies with innovative design and features. For
example, the system has color-coded, easy-to-understand menus and
self-contained reagents. The test tolerates temperature variations that occur
in rural clinics lacking refrigeration for sample storage due to limited electricity or water, and can provide results much
faster. The careHPV Test
was developed with support from PATH, an international
nonprofit organization, and is manufactured by QIAGEN in Shenzhen, China.
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The careHPV Test
already plays an important role in QIAGENcares, QIAGEN's collaborations
with NGOs and governments in which it helps expand access to high-quality
cervical cancer screening in resource-poor regions. For example,
tests for cervical cancer have been conducted on women in El Salvador using the careHPV Tests since 2012. The
test will also be used in other countries, including Vanuatu.
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Also as part of QIAGENcares, QIAGEN and the Chittaranjan
National Cancer Institute (CNCI) started a five-year-program in 2010
to provide cervical cancer screening with the digene HC2 HPV Test to 50,000 women in rural
West Bengal. Screening is facilitated through mobile field clinics. This
project has screened more than 36,000 women to date and has detected 216 cases
of High Grade Squamous Intra-epithelial Lesions (HSIL) and 52 cases of cervical
cancers. Most of the cervical cancers were at early treatable stages, and more
than 90% of these patients have been treated at CNCI. In addition, many doctors
and community-based healthcare workers have been trained in HPV screening.
This project is the first HPV based screening project in India, demonstrating
program aspects and successful implementation with clear deliverables.
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Cervical cancer is the second most common cancer among women
worldwide, and research has shown that 80% of new cases and deaths occur in
developing countries, where awareness of the disease and access to preventive
tests and medical treatment is low. In many low-resource areas,
cervical cancer has eclipsed breast cancer as the primary cancer killer of
women.
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To learn more about QIAGENcares please visit:
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About QIAGEN
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QIAGEN N.V., a Netherlands holding company, is the leading global
provider of Sample & Assay Technologies that are used to transform
biological materials into valuable molecular information. Sample technologies
are used to isolate and process DNA, RNA and proteins from biological samples
such as blood or tissue. Assay technologies are then used to make these
isolated biomolecules visible and ready for interpretation. QIAGEN markets more
than 500 products around the world, selling both consumable kits and automation systems
to customers through four customer classes: Molecular Diagnostics (human
healthcare), Applied Testing (forensics, veterinary testing and food safety),
Pharma (pharmaceutical and biotechnology companies) and Academia (life sciences
research). As of December 31, 2013, QIAGEN employed approximately 4,000 people
in more than 35 locations worldwide. Further information can be found athttp://www.QIAGEN.com/.
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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, including without
limitation its expected operating results, are forward-looking, such statements
are based on current expectations and assumptions 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, regulatory
processes and dependence on logistics), variability of operating results and
allocations between customer classes, the commercial development of markets for
our products in applied testing, personalized healthcare, clinical research,
proteomics, women's health/HPV testing and nucleic acid-based molecular
diagnostics; 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
products; 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 and protect our products from
competitors' products; market acceptance of QIAGEN's new products, the
consummation of acquisitions, and the integration of acquired technologies and
businesses. For further information, please refer to the discussions in reports
that QIAGEN has filed with, or furnished to, the U.S. Securities and Exchange
Commission (SEC).
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