Full Press Release Details
| Deanne Eagle - Media Relations | 917.837.5866 |
| Susan Roush - Investor Relations | 818.222.8330 |
NEURALSTEM GRANTS FIRST LICENSES
FOR CNS THERAPY SURGICAL DEVICES
Industry-breakthrough Spinal
Platform and Floating Cannula Used in ALS Stem Cell Trial
ROCKVILLE, MD, September 6, 2012
-- Neuralstem, Inc. (NYSE MKT: CUR) announced that it has granted the first licenses for use of its Spinal Cord Delivery Platform
and Floating Cannula, for delivering therapeutic agents to the spinal cord, to Salt Lake City-based Q Therapeutics. This platform
and cannula have been in use since 2010, in the recently completed Phase I ALS trial delivering Neuralstem's NSI-566 neural
stem cells into the spinal cords of patients with amyotrophic lateral sclerosis, (ALS or Lou Gehrig's disease). The devices
have been demonstrated to be safe in the 18 industry-leading surgeries. Neuralstem holds the exclusive worldwide licenses to the
surgical devices. The financial terms of the agreement were not disclosed.
"This is the beginning of a new paradigm
in treating multiple indications for spinal cord diseases," said Richard Garr, Neuralstem's President and CEO.
"Intraspinal delivery of therapeutics has long been thought to pose problems too difficult to overcome. However, we have
established compelling safety data in our first-in-human, 18-patient trial, and we expect to continue to license out the surgical
devices to both industry and academia as they now begin to explore the possibilities our technology has enabled."
Neuralstem's patented technology enables
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 constitutively into mature, physiologically relevant human neurons and glia. Neuralstem has
recently completed an FDA-approved Phase I safety clinical trial for amyotrophic lateral sclerosis (ALS), often referred to as
Lou Gehrig's disease, and has been awarded orphan status designation by the FDA.
In addition to ALS, the company is also
targeting major central nervous system conditions with its NSI-566 cell therapy platform, including spinal cord injury, ischemic
spastic paraplegia and chronic stroke. The company has submitted an IND (Investigational New Drug) application to the FDA for a
Phase I safety trial in chronic spinal cord injury.
Neuralstem also has the ability to generate
stable human neural stem cell lines suitable for the systematic screening of large chemical libraries. Through this proprietary
screening technology, Neuralstem has discovered and patented compounds that may stimulate the brain's capacity to generate new
neurons, possibly reversing the pathologies of some central nervous system conditions. The company is in a Phase Ib safety
trial evaluating NSI-189, its first neurogenic small molecule compound, for the treatment of major depressive disorder (MDD). Additional
indications could include chronic traumatic encephalopathy (CTE), Alzheimer's disease, and post-traumatic stress disorder (PTSD).
For more information, please visit www.neuralstem.com
or connect with us on Twitter and Facebook.
Cautionary Statement Regarding Forward
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-K for the year ended December 31, 2011 and the quarterly report on Form 10-Q for the period
ended June 30, 2012.