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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Gyrate Atrophy Ocular and Systemic StudyAtrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, eye disorder, hereditary disease, optic choroid disorder, ornithine aminotransferase deficiency, uveal disorderActive, not recruitingNot stated2026-08-17NCT05312736

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