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CRISPR Therapeutics nabs grant to fund development of treatment for Friedreich's Ataxia

Published 10/13/2017, 10:10 AM
© Reuters.  CRISPR Therapeutics nabs grant to fund development of treatment for Friedreich's Ataxia
CRSP
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  • The Friedreich's Ataxia Research Alliance (FARA), a non-profit organization aimed at curing the inherited nervous system disorder, awards a grant to CRISPR Therapeutics (CRSP -3.8%) to support the development of CRISPR-Cas9 gene-editing approaches to FA.
  • The company will collaborate with the University of Alabama-Birmingham's Dr. Marek Napierala on the development of gene-editing reagents that will be evaluated in humanized animal models. CRISPR has the option to advance the compounds into clinical trials.
  • The dollar amount of the grant is not disclosed.
  • Now read: Athersys Partners Up: Can Nikon CeLL Get MultiStem On Track?


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