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NEWS Release
Wex Completes Tetrodin™ Trial Enrollment
Date: January 4, 2005
Toronto Stock Exchange
Trading Symbol: WXI
http://www.wexpharma.com
E-mail: wex@wexpharma.com
Vancouver,
Canada, (January 4, 2005) -
Wex Pharmaceuticals Inc. (TSX:WXI) is pleased to announce that it
has successfully completed the enrollment and dosing of patients
during the month of December for the ongoing Phase IIa opioid dependence
study with Tetrodin™ (Wex's proprietary formulation of Tetrodotoxin-TTX).
This randomized, double-blind, placebo-controlled study evaluates
the safety and efficacy of Tetrodin™ in decreasing the severity
of withdrawal symptoms in opiate-dependent subjects who are receiving
methadone.
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
treatment for 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.
Results
of the Tetrodin™ study are expected to be released in the spring
of 2005.
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 Gordon Stanley, Corporate Communications
at 604-683-8880 or 1-800-722-7549.
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