FDA approves novel gene therapy to treat patients with a rare form of inherited vision loss

December 19, 2017

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SILVER SPRING, Md., Dec. 19, 2017 /PRNewswire-USNewswire/ — The U.S. Food and Drug Administration today approved Luxturna (voretigene neparvovec-rzyl), a new gene therapy, to treat children and adult patients with an inherited form of vision loss that may result in blindness. Luxturna is…

Category: Precious Metals