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GenSight Biologics Announces Regulatory Approval for GS010/LUMEVOQ® REVISE Dose-Ranging Study in France

PARIS, December 02, 2025--Regulatory News: GenSight Biologics (Euronext: SIGHT, ISIN: FR0013183985, PEA-PME eligible), a biopharma company focused on developing and commercializing innovative gene therapies for retinal neurodegenerative diseases and central nervous system disorders, today announced that the French medicines safety agency ANSM (Agence nationale de sécurité du médicament et des produits de santé) has authorized the dose-ranging study REVISE, which will investigate the efficacy and

articleGensight Biologics SaDecember 2, 20254/company/gensight-biologics-sa-1/news/gensight-biologics-announces-regulatory-approval-for-gs010lumevoqr-revise-dose-ranging-study-in-france-1
GenSight Biologics Announces Regulatory Approval for GS010/LUMEVOQ® REVISE Dose-Ranging Study in France

About this update from Gensight Biologics Sa

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Leber Hereditary Optic NeuropathyBiologicsREVISEgene therapiesclinical developmentEthics CommitteeRegulatory approvalthe Companyvision lossneurodegenerative diseasesmitochondrial diseaseANSM