Novogen Sales Up, Significant Advances With Clinical Trial Program
February 25 2005 - 11:46AM
PR Newswire (US)
Novogen Sales Up, Significant Advances With Clinical Trial Program
SYDNEY, Australia and STAMFORD, Conn., Feb. 25
/PRNewswire-FirstCall/ -- Half year results for pharmaceutical
company, Novogen Limited (NASDAQ:NVGN)(Australia: NRT), reflect
improved sales for the half-year to Dec. 31, 2004, and a marginal
increase in expenditure due to significant advances with human
clinical trials of its lead anti-cancer drug phenoxodiol. Cash
reserves at Dec. 31, 2004, stood at $38 million. Sales for the
half-year were $5.8 million, up six percent from $5.5 million for
the half-year ending Dec. 31, 2003. Total revenue for the half-year
was up 4.4 percent to $7.57 million compared with the previous
corresponding period. Royalties of approximately $0.87 million also
were received during the half-year under Novogen's soy patent
license agreement with Solae LLC, a joint venture between DuPont
and Bunge. During February, it was announced that Novogen had
agreed to the assignment of the license from Solae to the larger
company Archer Daniels Midland in the U.S. Net loss for the half
year was up $0.42 million to $3.70 million, compared with $3.28
million for the same period last year. Novogen Chief Executive
Officer, Mr. Christopher Naughton said marketing and selling
expense savings of $1.5 million over the previous corresponding
period were achieved with more targeted marketing of consumer
products but were offset by costs associated with the rapidly
expanding drug development program. The Novogen Group's leading
anti-cancer drug phenoxodiol is in Phase II human clinical trials
for the treatment of prostate and ovarian cancers and in addition
is in trials for renal cancer and cervical cancer, all through its
86.9 percent owned U.S. subsidiary, Marshall Edwards, Inc.
Phenoxodiol has also achieved "fast track" development status from
the U.S. Food and Drug Administration for use in both oral and
intravenous forms for the treatment of various cancers. This means
phenoxodiol has been made eligible for certain accelerated
marketing approval programs although it does not guarantee
regulatory approval. Phase III trials are now in planning. During
January, Yale University School of Medicine research also revealed
phenoxodiol enhanced the ability of another cancer drug to kill
human ovarian cancer cells in the laboratory. Mr. Naughton said
Novogen's ongoing strategy was to continue self-funding its drug
development program for as long as was commercially viable. "Our
present cash reserve position ensures that we can resist the need
to prematurely seek outside partnerships for drug development and
pharmaceutical licensing. We will however invoke our licensing plan
when it is in the best interests of our shareholders," Mr. Naughton
said. Novogen is focused on research and development of drugs
derived from its phenolic technology platform. The Company manages
its international research and development programs utilizing the
expertise and clinical research capabilities of universities and
hospitals in Australia, the U.S. and other key international
locations. 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: Novogen Limited
CONTACT: Mr. David Seaton, Chief Financial Officer, of Novogen
Limited, +011 (61) (02) 9878 0088; or David Sheon of SciWords, LLC,
+1-202-518-6321, for Novogen Limited
Copyright
Kazia Therapeutics (NASDAQ:KZIA)
Historical Stock Chart
From Jun 2024 to Jul 2024
Kazia Therapeutics (NASDAQ:KZIA)
Historical Stock Chart
From Jul 2023 to Jul 2024