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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
ATSN-201 Gene Therapy in RS1-Associated X-linked Retinoschisiseye disorder, retinal degeneration, retinal disorder, retinoschisisRecruitingPhase 32026-09-29NCT05878860
Study of Subretinally Injected ATSN-101 Administered in Patients With Leber Congenital Amaurosis Caused by Biallelic Mutations in GUCY2DEye Diseases, Hereditary, Leber congenital amaurosis, Leber congenital amaurosis 1, cone-rod dystrophy 6, eye disorder, littoral cell angioma of the spleen, retinal disorderActive, not recruitingPhase 1 / Phase 22026-08-03NCT03920007