The ongoing Phase II trial is a randomized, double-blind, placebo controlled multi-center study designed to evaluate the safety and efficacy of NurOwn(TM) in 48 ALS patients. The primary endpoint of the study is the safety of intrathecal and intramuscular administration of NurOwn(TM). Secondary endpoints include change in the ALS Functional Rating Scale (ALSFRS) and change in slow vital capacity (SVC). For further information, go to www.clinicaltrials.gov.
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UMass Memorial Medical Center is the advanced tertiary care referral center for Central New England. The Medical Center offers a full complement of sophisticated technology and support services necessary to provide the region with specialists renowned for their work in areas such as cardiology, cancer, diabetes and orthopedics. To learn more about UMass Memorial, please visit www.umassmemorial.org.
About BrainStorm Cell
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SOURCE: BrainStorm Cell Therapeutics