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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary diseaseRecruitingPhase 22026-09-28NCT07024693
A Multiple Ascending Dose Study of DT-216P2 in Patients With Friedreich's AtaxiaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Friedreich ataxia, Nutritional and Metabolic Diseases, Spinocerebellar Degenerations, brain disorder, central nervous system disorder, cerebellar disorder, hereditary disease, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, spinal cord disorderRecruitingPhase 1 / Phase 22025-05-18NCT06874010
A Single Ascending Dose Study of DT-216P2 in Normal Healthy ParticipantsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Friedreich ataxia, Nutritional and Metabolic Diseases, Spinocerebellar Degenerations, brain disorder, central nervous system disorder, cerebellar disorder, hereditary disease, inborn mitochondrial metabolism disorder, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, spinal cord disorderNot yet recruitingPhase 12025-02-21NCT06772870