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NEWS Release
Wex Initiates Phase IIa
Clinical Trial of Tetrodin™ for Reduction of Withdrawal Symptoms
in Opiate Dependent Patients
Date: November 15, 2004
Toronto Stock Exchange
Trading Symbol: WXI
http://www.wexpharma.com
E-mail: wex@wexpharma.com
Vancouver, Canada,
November 15, 2004 Wex Pharmaceuticals Inc. (TSX: WXI),
is pleased to announce that it has initiated a Phase IIa double-blind,
randomized, cross-over, placebo-controlled trial of Tetrodin™ (Wex's
proprietary formulation of Tetrodotoxin-TTX). This study is designed
to evaluate the safety and efficacy in decreasing the severity of
withdrawal symptoms in 20 opiate-dependent subjects who are receiving
metha don e in a treatment program. The first group of 10 patients
has been recruited and they are now receiving the treatment (tetrodotoxin/placebo).
The dosing period is expected to be completed before the end of
the year.
Opioid dependence is characterized
by a withdrawal syndrome that occurs when opioid agonists are abruptly
discontinued or their activity is antagonized. Managing withdrawal
is a critical step in initiating into treatment many patients who
are opioid dependent. Traditional medical management of opioid withdrawal
involves the substitution of a long-acting opioid for shorter-acting
opioids and gradual tapering.
The study is being led
by Dr. Edward Sellers, Director of Psychopharmacology and Dependence
Research Unit, Centre for Research in Women's Health, Sunnybrook
and Women's College Health Sciences Centre and President and CEO
of Ventana Clinical Research Corporation. Dr. Sellers is a member
of numerous national and international editorial boards governmental
advisory committees and international organizations including the
World Health Organization Expert Advisory Committee on Drug Dependence.
About Wex Pharmaceuticals
Inc.
Wex Pharmaceuticals Inc.
is a pharmaceutical company dedicated to the discovery of new therapeutic
agents for the treatment of moderate to severe pain, symptom relief
associated with addiction withdrawal from opioid abuse, and medicines
designed for local and regional anaesthesia. The Company's principle
business strategy is to derive drugs from naturally occurring toxins
and develop proprietary products for North American, European and
International markets. The Company also generates revenues from
sales of generic products manufactured at its facility in China
.
Forward Looking
Statement Disclaimer
Statements in this news release are forward-looking
statements which may not be based on historical fact, including
without limitation statements containing the words "believe", "may",
"plan", "will", "estimate", "anticipates", "intends", "expects"
and similar expressions. Such forward-looking statements involve
known and unknown risks, uncertainties and other factors that may
cause the actual results, events or developments to be materially
different from any future results, events or developments expressed
or implied by such forward-looking statements. Such factors include,
among others, WEX's stage of development, product revenues which
are difficult to predict, foreign currency exchange risk, additional
capital requirements, risks associated with the completion of clinical
trials, the ability to protect its intellectual property and dependence
on collaborative partners. These factors should be considered carefully
and readers are cautioned not to place undue rel ian ce on such
forward-looking statements. The company disclaims any obligation
to update any such factors or to publicly announce the result of
any revisions to any of the forward-looking statements contained
herein to reflect future results, events or developments.
For additional information on our products, visit us at www.wexpharma.com
or call Don Evans or Gor don Stanley, Corporate Communications
at 604-683-8880 or 1-800-722-7549.
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