SAN DIEGO, March 28, 2012 /PRNewswire/ -- Marshall
Edwards, Inc. (Nasdaq: MSHL), an oncology company focused on the
clinical development of novel therapeutics targeting cancer
metabolism, announced today that Daniel P.
Gold, Ph.D., President and Chief Executive Officer, will
present an update on Marshall
Edwards and the clinical development of its lead oncology
drug candidates, ME-143 and ME-344, at the Needham Healthcare
Conference on Wednesday, April 4,
2012 at 8:40 a.m. Eastern time
from the New York Palace Hotel. A live webcast of the presentation
can be accessed at www.marshalledwardsinc.com/investor. A replay
will be available approximately one hour after the
presentation.
About Marshall Edwards
Marshall Edwards, Inc. (Nasdaq:
MSHL) is a San Diego-based
oncology company focused on the clinical development of novel
therapeutics targeting cancer metabolism. The Company's lead drug
candidates, ME-143 and ME-344, have been shown to interact with
specific enzyme targets resulting in inhibition of tumor cell
metabolism, a function critical for cancer cell survival.
Marshall Edwards initiated a Phase I
clinical trial of intravenous ME-143 in patients with solid
refractory tumors in September 2011
and expects to collect final safety and pharmacokinetic data from
the trial by June 2012. The Company
submitted an Investigational New Drug application for ME-344 in
March 2012 and plans to initiate a
Phase I clinical trial of intravenous ME-344 in patients with solid
refractory tumors following approval by the FDA. For more
information, please visit www.marshalledwardsinc.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 or differences in interpretation 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.
SOURCE Marshall Edwards, Inc.
