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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Function and Imaging Assessments for G1961E-associated Stargardt DiseaseCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt Disease 1, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderActive, not recruitingNot stated2025-04-22NCT05674058

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OrganizationsLinked trials
University Hospital, Basel, Switzerland243

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Research sitesCityCountryLinked trials
University Hospital BaselBaselSwitzerland3