Marshall Edwards' US Patent Advance for Phenoxodiol
December 11 2006 - 9:19AM
PR Newswire (US)
WASHINGTON, Dec. 11 /PRNewswire-FirstCall/ -- Marshall Edwards,
Inc., (NASDAQ:MSHL) announces that, through its licensor, Novogen
Limited (NASDAQ:NVGN)(ASX:NRT), the Company has obtained allowance
for a composition patent for the anti-cancer drug candidate
phenoxodiol in the U.S. The U.S. Patent and Trademark Office has
allowed for grant claims to pharmaceutical compositions and unit
dose forms of various substituted isoflav-3-enes (including
phenoxodiol). The issue and publication fees have been paid and the
US patent is expected to issue in the first half of 2007. The
period of exclusivity is anticipated to be at least until 2017.
When granted, this patent will significantly add to the Novogen
intellectual property portfolio surrounding phenoxodiol, which
already includes granted protection for certain pharmaceutical uses
including the treatment of cancer, and pending patent applications
for manufacturing processes and modes of action. This portfolio
includes granted protection in the US, UK, Australia, Singapore,
New Zealand, Hong Kong, Czech Republic, and Turkey and pending
applications elsewhere around the world. The rights to develop and
commercialize phenoxodiol have been licensed to Novogen's US
oncology subsidiary company Marshall Edwards, Inc. Phenoxodiol is
now in a multi-national phase III clinical trial as a chemotherapy
resensitiser for advanced ovarian cancer and is known as the
'OVATURE' trial. Marshall Edwards Inc has recently appointed
JPMorgan Securities of New York to coordinate the international out
licensing and commercialization strategies for phenoxodiol. About
Phenoxodiol: Phenoxodiol is an investigational drug and, as such,
is not commercially available. Phenoxodiol is a novel-acting drug
that inhibits key pro-survival signaling pathways operating via
sphingosine-1-phosphate and Akt. Inhibition of these pathways leads
to prevention of phosphorylation of key anti-apoptotic proteins
such as XIAP. Loss of activity of these proteins restores the
ability of chemoresistant tumor cells to undergo apoptosis in
response to chemotherapy. The putative molecular target for
phenoxodiol is a tumor- specific protein, accounting for the highly
selective nature of the drug. About Novogen Novogen is an
Australian based biotechnology company in the business of research
and development of drugs derived from its phenolic technology
platform. The Company manages its research and development programs
utilizing the expertise and clinical research capabilities of
universities and hospitals in Australia, USA and Europe. Novogen's
drug program is researching and developing compounds for the
treatment of cancer, cardiovascular disease and anti inflammatory
disease. About Marshall Edwards Inc: Marshall Edwards, Inc.
(NASDAQ:MSHL) has licensed rights from Novogen Limited
(NASDAQ:NVGN) to bring three oncology drugs -- phenoxodiol, NV-196
and NV-143 -- to market globally. Marshall Edwards, Inc. is
majority owned by Novogen, an Australian biotechnology company that
is specializing in the development of therapeutics based on a
flavonoid technology platform. More information on phenoxodiol and
on the Novogen group of companies can be found at
http://www.marshalledwardsinc.com/ and http://www.novogen.com/.
Under U.S. law, a new drug cannot be marketed until it has been
investigated in clinical trials and approved by the FDA as being
safe and effective for the intended use. Statements included in
this press release that are not historical in nature are
"forward-looking statements" within the meaning of the "safe
harbor" provisions of the Private Securities Litigation Reform Act
of 1995. You should be aware that our actual results could differ
materially from those contained in the forward-looking statements,
which are based on management's current expectations and are
subject to a number of risks and uncertainties, including, but not
limited to, our failure to successfully commercialize our product
candidates; costs and delays in the development and/or FDA
approval, or the failure to obtain such approval, of our product
candidates; uncertainties in clinical trial results; our inability
to maintain or enter into, and the risks resulting from our
dependence upon, collaboration or contractual arrangements
necessary for the development, manufacture, commercialization,
marketing, sales and distribution of any products; competitive
factors; our inability to protect our patents or proprietary rights
and obtain necessary rights to third party patents and intellectual
property to operate our business; our inability to operate our
business without infringing the patents and proprietary rights of
others; general economic conditions; the failure of any products to
gain market acceptance; our inability to obtain any additional
required financing; technological changes; government regulation;
changes in industry practice; and one-time events. We do not intend
to update any of these factors or to publicly announce the results
of any revisions to these forward-looking statements. DATASOURCE:
Marshall Edwards, Inc. CONTACT: Christopher Naughton, CEO Marshall
Edwards, Inc., +011 612 8877 6196; or David Sheon of SciWords, LLC,
+1-202-518-6321, for Marshall Edwards, Inc. Web site:
http://www.marshalledwardsinc.com/ http://www.novogen.com/
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