Disclosure of Shareholdings in Accordance with Stock Market Rules
SOURCE:
Addex Pharmaceuticals
2008-08-05 10:40:00
Disclosure of Shareholdings in Accordance with Stock Market Rules
GENEVA, SWITZERLAND–(EMWNews – August 5, 2008) – Addex Pharmaceuticals (
announced today that on July 31, 2008, The Swiss Helvetia Fund,
Inc.
1270 Avenue of the Americas, Suite 400, New York, NY 10020,
U.S.A.,
has informed of exceeding the threshold of 5% in the shareholding
of
Addex Pharmaceuticals Ltd., holding a total of 314,860 registered
shares, corresponding to 5.37% of the voting rights.
About Addex
Addex Pharmaceuticals discovers and develops allosteric
modulators
for human health. Allosteric modulators are an emerging class
of
orally available small molecule therapeutic agents that we
believe
will offer patients better results than classical drugs.
Most
marketed drugs bind receptors where the body’s own natural
molecular
activators (i.e. endogenous ligands) bind, specifically to a key
part
of each receptor’s anatomy called the “active site”. In short,
most
drugs must out-compete endogenous ligands for the active site.
By
contrast, allosteric modulators are non-competitive because they
bind
receptors and modify their function even if the endogenous
ligand
also is binding it. In addition, because of this,
allosteric
modulators aren’t limited to simply turning a receptor on or off,
the
way most drugs are. Instead, they act more like a dimmer
switch,
offering control over the degree of activation or deactivation,
while
offering the body the ability to maintain control over
initiating
receptor activation. Furthermore, the allosteric approach
generally
affords freedom to operate – even on well-known, clinically
validated
targets – because the intellectual property surrounding
allosteric
chemistry and the allosteric sites on receptors is most
often
un-exploited.
ADX10059, our most advanced product, is an mGluR5 NAM
(metabotropic
glutamate receptor 5 negative allosteric modulator). It
has
demonstrated clinically and statistically significant efficacy
in
separate Phase IIa clinical trials in gastroesophageal reflux
disease
(GERD) patients and migraine headache patients and has potential
in
additional indications.
The Addex allosteric modulation discovery and development
platform
have been additionally validated through three seperatate
product
license or collaboration agreements with Merck & Co., Inc.
and
Johnson & Johnson as well as investments by Roche Ventures and
SR
One, the venture investment arm of GlaxoSmithKline.
Disclaimer
The foregoing release contains forward-looking statements that can
be
identified by terminology such as “not approvable”,
“continue”,
“believes”, “believe”, “will”, “remained open to exploring”,
“would”,
“could”, or similar expressions, or by express or implied
discussions
regarding Addex Pharmaceuticals Ltd, its business, the
potential
approval of its products by regulatory authorities, or
regarding
potential future revenues from such products. Such forward-
looking
statements reflect the current views of Addex Pharmaceuticals
Ltd
regarding future events, and involve known and unknown
risks,
uncertainties and other factors that may cause actual results
with
allosteric modulators of mGluR4, mGluR2, mGluR5 or other
therapeutic
targets to be materially different from any future
results,
performance or achievements expressed or implied by such
statements.
There can be no guarantee that allosteric modulators of
mGluR4,
mGluR2 or mGluR5 will be approved for sale in any market or by
any
regulatory authority. Nor can there be any guarantee that
allosteric
modulators of mGluR4, mGluR2, mGluR5 or other therapeutic
targets
will achieve any particular levels of revenue (if any) in the
future.
In particular, management’s expectations regarding
allosteric
modulators of mGluR4, mGluR2, mGluR5 or other therapeutic
targets
could be affected by, among other things, unexpected actions by
our
partners, unexpected regulatory actions or delays or
government
regulation generally; unexpected clinical trial results,
including
unexpected new clinical data and unexpected additional analysis
of
existing clinical data; competition in general; government,
industry
and general public pricing pressures; the company’s ability to
obtain
or maintain patent or other proprietary intellectual
property
protection. Should one or more of these risks or
uncertainties
materialize, or should underlying assumptions prove incorrect,
actual
results may vary materially from those anticipated,
believed,
estimated or expected. Addex Pharmaceuticals is providing
the
information in this press release as of this date and does
not
undertake any obligation to update any forward-looking
statements
contained in this press release as a result of new
information,
future events or otherwise.
Copyright © Hugin AS 2008. All rights reserved.
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