GENEVA, SWITZERLAND--(Marketwire - July 03, 2012) - Addex Therapeutics /
Addex Appoints Dr. Graham Dixon as Chief Scientific Officer and Head of
Research
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Geneva, Switzerland, 3 July 2012 - Addex Therapeutics (SIX: ADXN), a
leading
company pioneering allosteric modulation-based oral small molecule
drug
discovery and development, announced today the appointment of Dr. Graham
Dixon
to the newly created position of Chief Scientific Officer and Head of
Research.
Dr. Dixon will report directly to Dr. Bharat Chowrira, CEO of Addex, and
will
be responsible for leading all aspects of research and non-clinical
development
activities at Addex.
"We are delighted to have Graham join the Addex team. Graham has a
strong
background and an impressive track record in small molecule
pharmaceutical
research and development. He has been responsible for the discovery of
novel
drugs and steering their development from basic science into
clinical
development, as well as bringing products through mid-stage
proof-of-concept clinical trials." stated Dr. Bharat Chowrira, CEO of
Addex. "Addex' strength lies in our leading allosteric modulation
technology and the ability to leverage this platform to develop drug
candidates against previously undruggable but important validated
biological targets. Graham's experience and R&D leadership will be
instrumental as we execute on our core strategy and continue to build a
robust proprietary pipeline of high value drug discovery and
development programs and rapidly advancing these drug candidates towards
the clinic"
Dr. Dixon joins Addex with more than 20 years of experience in
pharmaceutical
researc, most recently as Chief Scientific Officer at Galapagos NV. In
this
role, Dr. Dixon was responsible for all research & early development
within the
company in multiple therapeutic areas as well as the management of more
than
260 scientific personnel across three sites in the Netherlands,
Belgium and
France. Prior to Galapagos, Dr. Dixon was Chief Scientific Officer at
Entomed
SA, a developer of natural anticancer and anti-infective agents. Dr.
Dixon
joined Entomed from a similar role at antifungal therapeutic company, F2G
Ltd.
Before joining F2G, Dr. Dixon held several roles at AstraZeneca starting
as a
project manager in anti-infective research and culminating in the role of
Global
Product Director in the oncology division. He started his career as
Head of
Biochemistry at Dowelanco (UK) Ltd. Dr. Dixon earned his PhD in
biochemistry
from the University of Swansea and a BSc in applied biology from the
University
of Bradford.
"I am excited about joining Addex, the recognized industry leader in
allosteric
modulation-based oral small molecule drug discovery and development,"
said Dr.
Dixon. "I look forward to building on the significant progress made
by the
world-class scientists at Addex and applying this powerful platform
towards
creating an attractive engine of innovative product candidates for the
treatment
of serious diseases and indications with a huge unmet medical need."
Addex Therapeutics (www.addextherapeutics.com) discovers and
develops an
emerging class of small molecule drugs, called allosteric modulators, which
have
the potential to be more specific and confer significant therapeutic
advantages
over conventional "orthosteric" small molecule or biological drugs. The
Company
uses its proprietary discovery platform to address receptors and other
proteins
that are recognized as attractive targets for modulation of important
diseases
with unmet medical needs. The Company's two lead products are being
investigated
in Phase 2 clinical testing: dipraglurant (ADX48621, an mGluR5
negative
allosteric modulator or NAM) is being developed by Addex to treat
Parkinson's
disease levodopa-induced dyskinesia (PD-LID); and ADX71149 (mGluR2
positive
allosteric modulator or PAM) is being developed by Addex' partner
Janssen
Pharmaceuticals Inc. to treat schizophrenia and anxiety seen in
patients
suffering from major depressive disorder. Addex also is advancing
several
preclinical programs including: GABA-BR PAM for overactive bladder,
pain and
other disorders; mGluR4 PAM for Parkinson's, MS, anxiety and other
diseases;
GLP1R PAM for type 2 diabetes; and mGluR2 NAM for treating Alzheimer's
disease
and depression. In addition, Addex has discovery programs to identify
allosteric
modulators of: receptor tyrosine kinase (RTK) superfamily, including
TrkB PAM
for treating neurodegenerative diseases (e.g. Alzheimer's,
Parkinson's and
Huntington's diseases); and TNF receptor superfamily, including TNFR1
NAM for
inflammation (e.g. rheumatoid arthritis) and other diseases.
Disclaimer: The foregoing release may contain 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
Therapeutics, formerly known as, Addex Pharmaceuticals, 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 Therapeutics regarding future events,
future
economic performance or prospects, and, by their very nature, involve
inherent
risks and uncertainties, both general and specific, whether known or
unknown,
and/or any other factor that may materially differ from the plans,
objectives,
expectations, estimates and intentions expressed or implied in such
forward-looking statements. Such may in particular cause actual results
with allosteric
modulators of mGluR2, mGluR4, mGluR5, GABABR, GLP1R, TNFR1, TrkB 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 mGluR2, mGluR4, mGluR5,
GABABR,
GLP1R, TNFR1, TrkB or other therapeutics targets will be approved for
sale in
any market or by any regulatory authority. Nor can there be any guarantee
that
allosteric modulators of mGluR2, mGluR4, mGluR5, GABABR, GLP1R, TNFR1,
TrkB 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 mGluR2, mGluR4, mGluR5, GABABR, GLP1R, TNFR1, TrkB 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 Therapeutics 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, except as may be required by
applicable
laws.
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originality of the information contained therein.
Source: Addex Therapeutics via Thomson Reuters ONE
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