STZ eyetrial

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
PDE6A Gene Therapy for Retinitis Pigmentosa	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosa	Active, not recruiting	Phase 1 / Phase 2	2024-04-18		NCT04611503
Safety and Efficacy of rAAV.hCNGA3 Gene Therapy in Patients With CNGA3-linked Achromatopsia	Eye 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 disorder	Active, not recruiting	Phase 1 / Phase 2	2024-04-18		NCT02610582

Clinical trials