Neuralstem Files FDA Application for First ALS Stem Cell Trial
18 Décembre 2008 - 3:51PM
PR Newswire (US)
ROCKVILLE, Md., Dec. 18 /PRNewswire-FirstCall/ -- Neuralstem, Inc.
(NYSE Alternext US: CUR) announced this morning that it has filed
an Investigational New Drug (IND) application with the U.S. Food
and Drug Administration (FDA) to begin a clinical trial to treat
amyotrophic lateral sclerosis (ALS or Lou Gehrig's disease). The
Company is planning to treat ALS patients through spinal injections
of its stem cells via its patented Human Neural Stem Cell
technology. (Logo:
http://www.newscom.com/cgi-bin/prnh/20061221/DCTH007LOGO ) "Like
all first human trials, this proposed trial is primarily designed
to test the safety and feasibility of both our stem cells and our
method of delivering the cells to the spinal cord in ALS patients,"
said Neuralstem CEO and President, Richard Garr. "We are also
proposing secondary endpoints which we hope will be able to measure
a slowing down of the degenerative process." ALS is a progressive
neurodegenerative disease that affects nerve cells in the brain,
leading to the degeneration and death of the motor neurons in the
spinal cord that control the muscles. Loss of the ability to
initiate and control muscle movement ends in paralysis and,
ultimately, death. ALS affects roughly 30,000 people in the U.S.,
with about 7,000 new diagnoses per year. Neuralstem expects to
conduct the trial at Emory University with Dr. Johnathan Glass,
M.D., Director of the Emory Neuromuscular Laboratory and Director
of the Emory ALS Center, as site Principal Investigator (PI). Dr.
Eva Feldman, M.D., Ph.D., Head of the A. Alfred Taubman Medical
Research Institute and the De Jong Professor of Neurology at the
University of Michigan Medical School, will be the overall PI for
the ALS trial program. Formal approvals from these institutions to
conduct the trial can come only after FDA approval of the trial
protocol. "The filing of this IND is an important event for
Neuralstem," said Garr, "but it marks only the beginning of a
process which includes working together with the FDA to approve the
first human ALS stem cell trial; refining our understanding of how
to optimize delivery of our cells into patients; and ultimately
delivering a new treatment for patients with this currently
incurable disease." About Neuralstem Neuralstem's patented
technology enables, for the first time, the ability to produce
neural stem cells of the human brain and spinal cord in commercial
quantities, and the ability to control the differentiation of these
cells into mature, physiologically relevant human neurons and glia.
Major Central Nervous System diseases targeted by the Company with
research programs currently underway include: Ischemic Spastic
Paraplegia, Traumatic Spinal Cord Injury, Huntington's disease and
ALS. The Company filed an IND (Investigational New Drug)
application with the FDA for ALS clinical trials in December, 2008,
and has entered into a collaborative agreement with
Albert-Ludwigs-University, in Freiburg, Germany, to develop
clinical trials for Huntington's disease. In pre-clinical work, the
company's cells have extended the life of rats with ALS (Lou
Gehrig's disease) as reported the journal TRANSPLANTATION, in
collaboration with Johns Hopkins University researchers, and also
reversed paralysis in rats with Ischemic Spastic Paraplegia, as
reported in NEUROSCIENCE on June 29, 2007, in collaboration with
researchers at University of California San Diego. Cautionary
Statement Regarding Forward Looking Information This news release
may contain forward-looking statements made pursuant to the "safe
harbor" provisions of the Private Securities Litigation Reform Act
of 1995. Investors are cautioned that such forward-looking
statements in this press release regarding potential applications
of Neuralstem's technologies constitute forward-looking statements
that involve risks and uncertainties, including, without
limitation, risks inherent in the development and commercialization
of potential products, uncertainty of clinical trial results or
regulatory approvals or clearances, need for future capital,
dependence upon collaborators and maintenance of our intellectual
property rights. Actual results may differ materially from the
results anticipated in these forward- looking statements.
Additional information on potential factors that could affect our
results and other risks and uncertainties are detailed from time to
time in Neuralstem's periodic reports, including the annual report
on Form 10-KSB for the year ended December 31, 2007 and the
quarterly report on form 10-Q for the period ended September 30,
2008. http://www.newscom.com/cgi-bin/prnh/20061221/DCTH007LOGO
http://photoarchive.ap.org/ DATASOURCE: Neuralstem, Inc. CONTACT:
Richard Garr, President of Neuralstem, Inc., +1-301-366-4960;
Media, Deanne Eagle of Planet Communications for Neuralstem, Inc.,
+1-917-837-5866; Investor Relations, Ina McGuinness of ICR, Inc.,
+1-310-954-1100, or Steve Chizzik of Equity Communications,
+1-908-688-9111, both for Neuralstem, Inc. Web site:
http://www.neuralstem.com/
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