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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Safety and Preliminary Efficacy of VG801 in Patients With ABCA4 Mutation-associated Retinal Dystrophy (Stargardt Disease)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt Disease 1, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 1 / Phase 22026-09-02NCT07002398

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OrganizationsLinked trials
VeonGen Therapeutics GmbH2

1 results · Page 1 of 1

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Research sitesCityCountryLinked trials
Shanghai General HospitalShanghaiChina59