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Voretigene neparvovec-rzyl (Luxturna) was approved by FDA in December of 2017 and is an adeno-associated virus vector-based gene therapy indicated for the treatment of patients with confirmed biallelic RPE65 mutation-associated retinal dystrophy

Studies on rodents and cells have been used to suggest that BPC-157 might help heal tissues like tendons, joints, nerves, the intestinal tract, stomach and skin, but these havent been supported by studies in humans

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