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November 7, 2006
Neurochem to report on third quarter of fiscal 2006 About Neurochem
Neurochem Inc. is focused on the development and commercialization of innovative therapeutics to address critical
unmet medical needs. Eprodisate (KIACTA; formerly FIBRILLEX) is currently being developed for the treatment
of AA amyloidosis, and is under regulatory review for marketing approval by the U.S. Food and Drug Administration and
European Medicines Agency. Tramiprosate (ALZHEMED), for the treatment of Alzheimer's disease, is currently in
Phase III clinical trials in both North America and Europe and tramiprosate (CEREBRIL), for the prevention of
Hemorrhagic Stroke caused by Cerebral Amyloid Angiopathy, has completed a Phase IIa clinical trial. To Contact Neurochem
For additional information on Neurochem and its drug development programs, please call the North American toll-free number
1 877 680-4500 or visit our Web Site at: www.neurochem.com.
Certain statements contained in this news release, other than statements of fact that are independently verifiable
at the date hereof, may constitute forward-looking statements. Such statements, based as they are on the current
expectations of management, inherently involve numerous risks and uncertainties, known and unknown, many of which are
beyond Neurochem's control. Such risks include but are not limited to: the impact of general economic conditions, general
conditions in the pharmaceutical industry, changes in the regulatory environment in the jurisdictions in which Neurochem
does business, stock market volatility, fluctuations in costs, and changes to the competitive environment due to
consolidation, as well as other risks disclosed in public filings of Neurochem. Consequently, actual future results
may differ materially from the anticipated results expressed in the forward-looking statements. The reader should not
place undue reliance, if any, on the forward-looking statements included in this news release. These statements speak
only as of the date made and Neurochem is under no obligation and disavows any intention to update or revise such
statements as a result of any event, circumstances or otherwise. Please see the Annual Information Form for further
risk factors that might affect the Company and its business.
For further Information, please contact: |
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