New Hope Network is part of the Informa Markets Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

Novogen Patent Granted in Canada

SYDNEY, Australia, May 20, 2004 /PRNewswire-FirstCall via COMTEX/ -- Pharmaceutical company, Novogen (NVGN) , has been granted patent coverage over its OTC products being sold in Canada.

The patent covers the isoflavone composition of the products Promensil(TM), Rimostil(TM) and Trinovin(TM). Additionally the patent covers the use of isoflavone health supplements for the treatment of menopause symptoms.

The CEO of Novogen, Mr. Christopher Naughton, said the grant of this patent significantly strengthens Novogen's position in the Canadian market.

"The issue of this Canadian patent will facilitate Novogen discussions with other companies now engaged in, or planning to enter the market in which Promensil, Rimostil and Trinovin compete in Canada," Mr. Naughton said.

This patent (# 2,136,233) covers isoflavones in health supplement tablets and capsules including those sourced from red clover and soy.

Novogen uses red clover as the source of the four types of isoflavones in its products, and has licensed to Solae LLC (a joint venture company of DuPont and Bunge), in most countries of the world including Canada, the rights to health supplements containing isoflavones extracted from soy.

The U.S. version of this patent as it relates to soy has already been granted, and under the license from Novogen, Solae has commenced patent litigation asserting infringement against a number of parties in the U.S.

More information on the Novogen group of companies and their associated technology developments can be found at and at

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.

Hide comments


  • Allowed HTML tags: <em> <strong> <blockquote> <br> <p>

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.