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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Safety and Efficacy of rAAV.hCNGA3 Gene Therapy in Patients With CNGA3-linked AchromatopsiaEye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, achromatopsia, color vision disorder, cone dystrophy, eye disorder, nervous system disorder, vision disorderActive, not recruitingPhase 1 / Phase 22024-04-18NCT02610582

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Research sitesCityCountryLinked trials
University Hospital Tuebingen, Center for OphthalmologyTübingenGermany1