Acorda Therapeutics, Inc. (Nasdaq:ACOR)
will host a Research and Development (R&D) Day for the investment
community on Tuesday, November 5, 2013 from 9:00 a.m. to 12:00 p.m. at
Alexandria Center for Life Sciences in New York City (450 East 29th
Street at First Avenue).
Members of Acorda’s management team, including President and CEO Ron
Cohen, M.D., Chief Scientific Officer Andrew Blight, Ph.D., Chief
Medical Officer Enrique Carrazana., M.D., and VP, Research and
Development Anthony Caggiano, M.D., Ph.D., will review Acorda’s six
clinical-stage programs. Presentations will include development programs
in post-stroke deficits, cluster seizures, heart failure, neuropathic
pain, multiple sclerosis and spinal cord injury.
Independent experts in the fields of heart failure, epilepsy, post
stroke deficits and remyelination will provide their perspectives on
disease state and current standards of care in their respective
therapeutic area.
A live audio webcast of the presentation can be accessed under “Investor
Events” in the Investor section of the Acorda website at www.acorda.com
or available via the following link prior to the start of the event:
http://www.media-server.com/m/p/ic98q9dq
The webcast of the presentation and copies of the slideshow will be
available after the event by accessing the Investor section of www.acorda.com.
About Acorda Therapeutics
Founded in 1995, Acorda Therapeutics is a biotechnology company focused
on developing therapies that restore function and improve the lives of
people with neurological conditions.
Acorda markets three FDA-approved therapies including: AMPYRA®
(dalfampridine) Extended Release Tablets, 10 mg, a treatment to improve
walking in patients with multiple sclerosis (MS); ZANAFLEX CAPSULES®
(tizanidine hydrochloride) and Zanaflex tablets, a short-acting drug for
the management of spasticity; and QUTENZA® (capsaicin) 8% Patch, for the
management of neuropathic pain associated with postherpetic neuralgia.
AMPYRA is marketed outside the United States as FAMPYRA®
(prolonged-release fampridine tablets) by Biogen Idec under a licensing
agreement from Acorda.
Acorda has one of the leading pipelines in the industry of novel
neurological therapies. The Company is currently developing six
clinical-stage therapies and one preclinical stage therapy that address
a range of disorders including post-stroke deficits, epilepsy, cerebral
palsy, stroke, peripheral nerve damage, spinal cord injury, neuropathic
pain, and heart failure. For more information, please visit the
Company’s website at: www.acorda.com.
Forward-Looking Statements
This press release includes forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995. All
statements, other than statements of historical facts, regarding
management's expectations, beliefs, goals, plans or prospects should be
considered forward-looking. These statements are subject to risks and
uncertainties that could cause actual results to differ materially,
including our ability to successfully market and sell Ampyra in the
U.S.; third party payers (including governmental agencies) may not
reimburse for the use of Ampyra or our other products at acceptable
rates or at all and may impose restrictive prior authorization
requirements that limit or block prescriptions; the risk of unfavorable
results from future studies of Ampyra or from our other research and
development programs, including Diazepam Nasal Spray or any other
acquired or in-licensed programs; we may not be able to complete
development of, obtain regulatory approval for, or successfully market
Diazepam Nasal Spray or other products under development; the occurrence
of adverse safety events with our products; delays in obtaining or
failure to obtain regulatory approval of or to successfully market
Fampyra outside of the U.S. and our dependence on our collaboration
partner Biogen Idec in connection therewith; competition, including the
impact of generic competition on Zanaflex Capsules revenues; failure to
protect our intellectual property, to defend against the intellectual
property claims of others or to obtain third party intellectual property
licenses needed for the commercialization of our products; failure to
comply with regulatory requirements could result in adverse action by
regulatory agencies; and the ability to obtain additional financing to
support our operations. These and other risks are described in greater
detail in Acorda Therapeutics' filings with the Securities & Exchange
Commission. Acorda may not actually achieve the goals or plans described
in its forward-looking statements, and investors should not place undue
reliance on these statements. Forward-looking statements made in this
release are made only as of the date hereof, and Acorda disclaims any
intent or obligation to update any forward-looking statements as a
result of developments occurring after the date of this release.
Copyright Business Wire 2013