** U.S.-listed shares of Swiss-based gene editing company
CRISPR Therapeutics AG CRSP.O up 5.1% at $65.8 premarket
** U.S. FDA late-Thursday accepted review of marketing
application for CRSP's experimental gene-editing therapy,
exa-cel, for two types of blood disorders - co
** CRSP is developing exa-cel with partner Vertex
Pharmaceuticals Inc VRTX.O as a potential one-time treatment,
which would be the first therapy to use the nobel-winning CRISPR
gene editing technology if approved
** FDA has granted priority review for the therapy in severe
sickle cell disease (SCD) and a standard review for
transfusion-dependent beta thalassemia (TDT)
** FDA is set to make a decision on the therapy's use in SCD
and TDT by December 8, 2023, and March 30, 2024, respectively -
co
** Separately on Friday, CRSP/VRTX reported updated data on
the therapy and said it met primary and key secondary study
goals at interim analyses of the trials
** Up to Thursday close, stock gained nearly 54% YTD
(Reporting by Pratik Jain in Bengaluru)
((Pratik.Jain@thomsonreuters.com;))