06.11.2007 11:45:00
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Neurogen Announces Aplindore Preclinical Data to Be Presented at Neuroscience 2007
Neurogen Corporation (Nasdaq: NRGN), a drug discovery and development
company, today announced that data from a preclinical study with
aplindore, the Company’s compound for the
treatment of Parkinson’s disease and restless
legs syndrome (RLS), will be presented on November 6 in a poster at
Neuroscience 2007, the Society for Neuroscience annual meeting in San
Diego, California.
The poster, "Aplindore, a novel potent
dopamine D2 receptor partial agonist is
efficacious as a monotherapy or when combined with L-DOPA in treating
motor disabilities in the MPTP
(1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine)-treated marmoset, a
non-human model of Parkinson's Disease,” will
be displayed at the San Diego Convention Center in Exhibit Halls B-H
during the "Parkinson’s
Disease: Dyskinesias” session on Tuesday,
November 6, from 4:00-5:00 p.m. PT (Poster Board Number: N14).
The number of patients diagnosed with Parkinson’s
disease and RLS continues to grow and Neurogen believes there is need
for improvement in side effect profiles and dosing regimen that may be
made possible by aplindore. Dopamine agonists currently available for
the treatment of Parkinson’s disease and RLS
are full agonists at D2 receptors and have many
significant side effects. In addition they require a long titration
period--up to seven weeks in Parkinson’s
disease and four to seven weeks in RLS.
The currently available D2 full agonist
treatments for Parkinson’s disease produce
side effects in many patients that include daytime somnolence or
drowsiness, dyskinesias (sudden episodes of abnormal involuntary
movements), and hallucinations. While these drugs have also proved
effective in the treatment of RLS, many patients still suffer side
effects of augmentation (a worsening of symptoms), nausea, constipation,
and hypotension. By avoiding over-stimulation of healthy parts of the
brain that is seen with the currently marketed D2
full agonists, Neurogen believes aplindore’s
partial agonist profile may provide an improved side-effect profile and
shorter dosing titration period in Parkinson’s
disease and RLS. The Company expects to commence Phase 2 trials in
Parkinson’s disease and Restless Legs
Syndrome (RLS) following the manufacture of clinical supplies of
aplindore.
About Neurogen
Neurogen Corporation is a drug discovery and development company
focusing on small molecule drugs to improve the lives of patients
suffering from disorders with significant unmet medical need, including
insomnia, obesity, pain, Parkinson’s disease,
restless legs syndrome (RLS), and depression. Neurogen conducts its
research and development independently and, when advantageous,
collaborates with world-class pharmaceutical companies to access
additional resources and expertise.
Neurogen Safe Harbor Statement The information in this press release contains certain
forward-looking statements, made pursuant to applicable securities laws,
which involve risks and uncertainties as detailed from time to time in
Neurogen's SEC filings, including its most recent 10-K. Such
forward-looking statements relate to activities, events or developments
that Neurogen believes, expects or anticipates will occur in the future
and include, but are not limited to, earnings estimates, statements that
are not historical facts relating to Neurogen’s
future financial performance, its growth and business expansion, its
financing plans, the timing and occurrence of anticipated clinical
trials, and potential collaborations or extensions of existing
collaborations. These statements are based on certain assumptions made
by Neurogen based on its experience and perception of historical trends,
current conditions, expected future developments and other factors it
believes are appropriate under the circumstances. Actual results
may differ materially from those expressed or implied by such
forward-looking statements as a result of various factors, including,
but not limited to, risks associated with the inherent uncertainty of
drug research and development, difficulties or delays in development,
testing, regulatory approval, production and marketing of any of
Neurogen's drug candidates, adverse side effects or inadequate
therapeutic efficacy or pharmacokinetic properties of Neurogen's drug
candidates or other properties of drug candidates which could make them
unattractive for commercialization, advancement of competitive products,
dependence on corporate partners, Neurogen’s
ability to retain key employees, sufficiency of cash to fund Neurogen's
planned operations and patent, product liability and third party
reimbursement risks associated with the pharmaceutical industry. Although
Neurogen believes that its expectations are based on reasonable
assumptions, it can give no assurance that the anticipated results will
occur. For such statements, Neurogen claims the protection of
applicable laws. Future results may also differ from previously
reported results. For example, positive results or safety and
tolerability in one clinical study provides no assurance that this will
be true in future studies. Forward-looking statements represent
the judgment of Neurogen’s management as of
the date of this release and Neurogen disclaims any intent and does not
assume any obligation to update or revise any forward-looking
statements, whether as a result of new information, future events or
otherwise, unless required under applicable law.
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