Executive Summary: Ophthalmic gene therapy clinical trials aim to correct or replace genes in the eye to slow, halt, or reverse inherited retinal diseases. Gene therapy has rapidly moved from concept to clinic in ophthalmology. The approval of voretigene neparvovec (Luxturna) for RPE65‑mediated retinal dystrophy demonstrated that targeted genetic...
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Website title: Drug and Biologic Contract Research Organization (CRO) | Medpace