FDA Approves OncoVista's Phase I Clinical Trial of New Drug Candidate (OVI-117) for Solid Tumors
10 July 2012 - 10:00PM
Marketwired
OncoVista Innovative Therapies, Inc. (OTCBB: OVIT), a
biopharmaceutical company engaged in the development and
commercialization of targeted cancer therapies, announced today
that the US Food and Drug Administration (FDA) granted approval for
the Company's investigational new drug (IND) application for its
L-nucleoside conjugate (OVI-117) drug candidate.
"The FDA's swift approval of our IND provides validation of
OncoVista's mission to be a leader in the development of more
efficacious and less toxic targeted cancer therapies," said
Alexander Weis, PhD., Chairman, President and CEO of OncoVista.
This will allow the Company to build and enhance our drug portfolio
to the benefit of shareholders and more importantly, patients. The
founding mission of OncoVista is to develop more effective and less
toxic drugs for cancer. This is an important milestone towards that
mission.
About OVI-117
OVI-117, a derivative of FdUMP/5-FU, is a Thymidylate Synthase
(TS) inhibitor with enhanced pharmacological properties resulting
in the retention of efficacy and the reduction of toxicity. It has
particular promise for colon, breast, gastric and prostate
tumors.
About OncoVista Innovative Therapies
Texas-based OncoVista Innovative Therapies, Inc. (OTCBB: OVIT),
founded in 2004, is a biopharmaceutical company engaged in the
development and commercialization of targeted cancer therapies
which are more efficacious and less toxic. For additional
information, please visit OncoVista's corporate website at
www.oncovista.com
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.
COMPANY CONTACT: Michael Moloney Chief Operating Officer
(210) 677-6000
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