Published:
Agendia Launches TargetPrint(R) for Breast Cancer Patients
Optimizing Patient Identification for Targeted Therapies
That Ensure Benefits of Personalized Treatment
HUNTINGTON BEACH, Calif., andAMSTERDAM, Netherlands, Sept. 4 /PRNewswire/
-- Agendia, a world leader in molecular cancer diagnostics, today announced
the launch of TargetPrint(R), a new diagnostic test that allows physicians to
quantitatively determine the gene expression levels of the estrogen receptor
(ER), progesterone receptor (PR) and Human Epidermal growth factor Receptor 2
(HER2) in breast cancer tumor biopsies. The accurate measurement of these
receptors is of paramount importance in planning treatment of breast cancer
patients after surgery and assists physicians and patients in making informed
treatment decisions. TargetPrint runs on Agendia's new High Density Chip,
which received market clearance last month (August 2008) from the U.S. Food
and Drug Administration (FDA).
"Currently available targeted therapies, such as hormone treatments, can
have a huge impact on the survival and quality of life of a significant number
of breast cancer patients," said Bernhard Sixt, Ph.D., president and chief
executive officer of Agendia. "TargetPrint will play a key role in defining
which patients are most likely to benefit from these treatments."
"The test's results give a precise molecular read-out of prognostic
parameters for breast cancer and provide physicians and patients with reliable
guidance on the most suitable treatment for each individual patient," said
Richard A. Bender, MD, FACP, chief medical officer of Agendia. "In the near
future, it is our plan to add information on a wider range of drug targets to
TargetPrint and clinically validate these with key customers."
Agendia will present clinical data on TargetPrint at The 2008 Breast
Cancer Symposium which is co-sponsored by the American Society of Clinical
Oncology (ASCO) and will be held inWashington, DC from September 5-7, 2008.
TargetPrint is processed at Agendia's Clinical Laboratory Improvement
Amendments (CLIA) certified and the College of American Pathology (CAP)
accredited laboratory.
About Agendia
Agendia is a world leader in molecular cancer diagnostics. The company
markets four products based on its breakthrough platform for tumor gene
expression profiling and has several new diagnostic tests under development.
Agendia was the first company to receive FDA clearance for a breast cancer
test, MammaPrint(R), that predicts the risk of breast cancer recurrence. In
addition, the company collaborates with pharma companies to develop highly
effective personalized drugs in the area of oncology. Agendia is based in
Huntington Beach, California, and inAmsterdam, The Netherlands. For more
information on Agendia, please visit www.agendia.com.
MEDIA CONTACTS
U.S. Media Contact: EU and non-U.S. Media:
Kelly Connor Hans Herklots
Vice President Head Corporate Communications
Ogilvy Public Relations Worldwide Agendia
+1.212.880.5328 Office +31.20.462.1557 Office
+1.609.221.5785 Mobile +31.620.083.509 Mobile
Kelly.connor@ogilvypr.com hans.herklots@agendia.com
SOURCE Agendia
Copyright © 2008, PRNewswire
Copyright © 2008, NewsBlaze,
Daily News
Tags: ,HEA,MTC,PDT,TRI,WOM,CA-Agendia-Launches
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