ROCKVILLE, Md., Jan. 4, 2013 /PRNewswire/ -- Neuralstem, Inc. (NYSE MKT: CUR) announced that President and CEO Richard Garr will present at the fifth annual Biotech Showcase in San Francisco on Tuesday, January 8, 3:45 p.m. PT, in Room Powell. Garr will present a business overview, including a first look at the Phase I/II Stroke/NSI-566 cell therapy trial expected to commence in Beijing within several weeks. Garr will also provide an update on the company's ALS cell therapy trial and plans for the Phase II. The trial's investigators recently announced a substantial grant for the Neuralstem ALS Phase II trial from the National Institutes of Health (NIH). Garr will also update the trial progress of its first-in-class neurogenic NSI-189 small molecule drug which stimulates new neuron growth in the hippocampus, currently in a Phase Ib major depressive disorder (MDD) trial.
The audio webcast will be available in real-time at http://www.media-server.com/m/p/y46fee25 and archived for one year. The webcast link will also be posted on the Investor Center home page on Neuralstem's website: www.neuralstem.com.
The 2013 Biotech Showcase will be held at the Parc 55 Wyndham Hotel in San Francisco, January 7-9. For more information, see: http://www.ebdgroup.com/bts/index.php.About Neuralstem 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 completed dosing of the last patient in an FDA-approved Phase I safety clinical trial for amyotrophic lateral sclerosis (ALS), often referred to as Lou Gehrig's disease, in August 2012; the trial ends six months after that last surgery. Neuralstem has been awarded orphan status designation by the FDA for its ALS cell therapy. 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 stroke and glioblastoma (brain cancer). The company has submitted an IND (Investigational New Drug) application to the FDA for a Phase I safety trial in spinal cord injury.