LUXTURNA
voretigene neparvovec-rzyl
Manufacturer: Spark Therapeutics, Inc.
FDA-Approved Indications (1)
indicated for the treatment of patients with confirmed biallelic RPE65 mutation-associated retinal dystrophy
Population: all ages
Indications & Usage
1 INDICATIONS AND USAGE LUXTURNA (voretigene neparvovec-rzyl) is an adeno-associated virus vector-based gene therapy indicated for the treatment of patients with confirmed biallelic RPE65 mutation-associated retinal dystrophy. Patients must have viable retinal cells as determined by the treating physician(s). LUXTURNA is an adeno-associated virus vector-based gene therapy indicated for the treatment of patients with confirmed biallelic RPE65 mutation-associated retinal dystrophy. Patients must have viable retinal cells as determined by the treating physician(s). ( 1 )
💙 Support Programs
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