Inflammation after Voretigene Neparvovec Administration in Patients with RPE65-Related Retinal Dystrophy
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference12 articles.
1. Genetic basis of inherited retinal disease in a molecularly characterized cohort of more than 3000 families from the United Kingdom;Pontikos;Ophthalmology,2020
2. Inherited retinal diseases: therapeutics, clinical trials and end points—A review;Georgiou;Clin Exp Ophthalmol,2021
3. The natural history of inherited retinal dystrophy due to biallelic mutations in the RPE65 gene;Chung;Am J Ophthalmol,2019
4. Voretigene neparvovec in patients with RPE65 mutation-associated inherited retinal dystrophy: baseline characteristics from the real-world, prospective, observational PERCEIVE study;Fischer;Invest Ophthalmol Vis Sci,2021
5. Perifoveal chorioretinal atrophy after subretinal Voretigene Neparvovec-rzyl for RPE65-mediated Leber congenital amaurosis;Gange;Ophthalmol Retina,2022
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1. Interim safety and efficacy of gene therapy for RLBP1-associated retinal dystrophy: a phase 1/2 trial;Nature Communications;2024-09-10
2. Dose-Dependent Progression of Chorioretinal Atrophy at the Injection Site After Subretinal Injection of rAAV2/8 in Nonhuman Primates;Ophthalmology Science;2024-09
3. An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI Study;Human Gene Therapy;2024-08-01
4. Myopic Macular Hole and Detachment after Gene Therapy in Atypical RPE65 Retinal Dystrophy: A Case Report;Genes;2024-07-04
5. Objective Outcomes to Evaluate Voretigene Neparvovec Treatment Effects in Clinical Practice;Ophthalmology Retina;2024-07
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