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Spark gene therapy wins unanimous FDA panel vote

On Oct. 12, FDA's Cellular, Tissue and Gene Therapy Advisory Committee voted 16-0 that the benefit-risk profile for Luxturna voretigene neparvovec from Spark Therapeutics Inc. (NASDAQ:ONCE) supports the gene therapy's approval to treat biallelic retinal pigment epithelium-specific protein 65kDa (RPE65) mutation-associated retinal

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