OncoVista (OVIT.OB) Subsidiary Inks Exclusive Agreement with TATAA Molecular Diagnostics
2010年1月26日 - 10:00PM
ビジネスワイヤ(英語)
OncoVista Innovative Therapies, Inc. (OTCBB:OVIT) announced
today that its wholly owned subsidiary, AdnaGen AG, the
manufacturer of CE-certified circulating tumor cell (CTC)
diagnostic assays, has entered into an agreement with TATAA
Molecular Diagnostics, for the exclusive use of its Adnatest™
BreastCancer assays in an international breast cancer research
COHERTA project. TATAA Molecular Diagnostics and its partner, the
Institute of Biotechnology of the Czech Academy of Science, are
funding the COHERTA study through a grant obtained from the Czech
and Slovak subsidiaries of Hoffmann-La Roche the global drug
manufacturer.
TATAA Molecular Diagnostics together with the Czech Academy of
Science have been engaged in research since 2008 and have proven
the effectiveness of AdnaGen AG new prognostic and predictive
biomarkers. The purpose of this COHERTA project is to identify
additional applications for the CTC-test in clinics.
The international COHERTA study is expected to take three years
to complete and will be conducted in the Czech Republic and
Slovakia. The COHERTA study will focus on the most aggressive type
of breast cancer, HER2, which is diagnosed in one out of three
breast cancers. COHERTA intends to evaluate the relationship
between the HER2 status of the metastasic tumors and the HER2
status of the circulating tumor cells using the Adnatest™
BreastCancer assay. The HER2 status is known to be a crucial marker
for disease prognosis and therapy choice and it is established,
that it may change from negative to positive throughout the disease
progression. It has been reported that there is a significant
number of patients who exhibit HER2-positive metastases who
originally had HER2 negative tumors. Currently, the only way to
evaluate the HER2-status of a tumor is through a biopsy of the
tumor tissue.
The COHERTA study believes it can monitor circulating tumor
cells with the Adnatest™ BreastCancer assay to identify the HER2
type of metastases, This would be a new and important application
of the Adnatest™ BreastCancer blood test for patients with breast
cancer relapse.
In addition, the COHERTA study team also believes that some
patients might then benefit from biological therapy if their cancer
type is characterized as HER2-positive. Herceptin, a biological
therapy produced by Hoffman-La Roche, is typically prescribed to
patients with HER2-positive tumor types.
The Czech team running the COHERTA study believes that analyzing
CTC in peripheral blood may provide minimal invasive and more
cost-effective diagnostic tools to reassess the HER2 status. “One
can simply argue, that the CTC are most likely disseminated from
the metastatic lesion and hence they should reflect its phenotype,”
Dr. Ales Tichopad, the COHERTA coordinator says.
“OncoVista Innovative Therapies, Inc. is very pleased that
AdnaGen’s Adnatest™ BreastCancer assays are being used exclusively
in the COHERTA study. This next phase is another important step in
identifying blood-based diagnostic and monitoring assays that work
to the patient’s benefit,” said Dr. Alexander L. Weis, President
and CEO of OncoVista. “The Adnatest™ BreastCancer is just one of
several on which OncoVista has been working on. It’s subsidiary,
AdnaGen AG, has also been developing and testing other CE-certified
circulating tumor cell (CTC) diagnostic assays for prostate and
colon cancers. Together with breast cancers, prostate and colon
cancers are the three most frequent types of cancer diagnosed
today.”
“In these economic times,” said Dr. Weis, “when drug companies,
insurance providers, and patients are looking for better ways to
test the effectiveness of oftentimes expensive, cancer therapies, a
diagnostic blood test such as the Adnatest™ BreastCancer, can lead
to better evaluation sooner and more cost-effective treatments with
less, unnecessary suffering and toxic side-effects.”
OncoVista Innovative Therapies, Inc. is a biopharmaceutical
company involved in the development of targeted anticancer
therapies by using tumor-associated biomarkers. In conjunction with
its subsidiary, AdnaGen AG which is based in Langenhagen, Germany,
the Company has developed and currently markets patented diagnostic
kits in Europe for the detection of circulating tumor cells in
patients with breast, colon, ovarian and prostate cancers under the
brand name AdnaGen™. The Company has also developed research
products for the detection of steroid receptors and cancer stem
cells and has research contracts in place with major pharmaceutical
companies and recognized U.S. research facilities.
OncoVista has an experienced management team specialized in the
development of targeted, anticancer drugs led by Dr. Alexander L.
Weis. OncoVista’s targeted drug development uses the proprietary,
state-of-the-art molecular platform of AdnaGen AG.
Forward-Looking Statements: A number of statements contained in
this press release are forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995
that involve risks and uncertainties that could cause actual
results to differ materially from those expressed or implied in the
applicable statements. These risks and uncertainties that could
cause actual results to differ materially from those expressed or
implied in the applicable statements.
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