Eye Diseases, Hereditary (DBCOND0042563)

Identifiers

Synonyms
Eye Diseases Hereditary / Eye Disease, Hereditary / Hereditary Eye Disease

Associated Data

Indicated Drugs and Targets
Not Available
Clinical Trials
IdentifierTitleDrug(s)PurposePhaseStatus
NCT02435940
Inherited Retinal Degenerative Disease RegistryNo drug interventionsNot AvailableNot Availablerecruiting
NCT01399515
Efficacy and Safety of Oral Valproic Acid for Retinitis Pigmentosatreatment2completed
NCT04765345
Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1FNo drug interventionsNot AvailableNot Availableactive_not_recruiting
NCT03913130
Extension Study to Study PQ-110-001 (NCT03140969)treatment1 / 2terminated
NCT06627179
Study to Evaluate Ultevursen in Subjects with Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A Genetreatment2not_yet_recruiting
NCT05573984
Natural History of PRPF31 Mutation-Associated Retinal DystrophyNo drug interventionsNot AvailableNot Availablerecruiting
NCT02946879
Long-Term Follow-Up Gene Therapy Study for Leber Congenital Amaurosis OPTIRPE65 (Retinal Dystrophy Associated With Defects in RPE65)No drug interventionsNot AvailableNot Availablecompleted
NCT06162585
Non-Interventional Long Term Follow-up Study of Participants Previously Enrolled in the RESTORE StudyNo drug interventionsNot AvailableNot Availableenrolling_by_invitation
NCT02203682
Doxycycline Treatment in Mild Thyroid-Associated Ophthalmopathytreatment2unknown_status
NCT01727973
Efficacy of Subantimicrobial Dose Doxycycline for Moderate to Severe and Active Graves' Orbitopathytreatment1 / 2completed
NCT04945772
Efficacy and Safety of MCO-010 Optogenetic Therapy in Adults With Retinitis Pigmentosa [RESTORE]No drug interventionstreatment2completed
NCT00811512
Fundus Changes in the Microphthalmy EyesNo drug interventionsNot AvailableNot Availablecompleted
NCT03872479
Single Ascending Dose Study in Participants With LCA10treatment1 / 2active_not_recruiting
NCT03396042
Natural History Study of CEP290-Related Retinal DegenerationNo drug interventionsNot AvailableNot Availablecompleted
NCT05176717
Study to Evaluate the Efficacy Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene With Early to Moderate Vision Loss (Celeste)treatment2 / 3terminated
NCT05158296
Study to Evaluate the Efficacy Safety and Tolerability of Ultevursen in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene (Sirius)treatment2 / 3terminated
NCT03780257
Study to Evaluate Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Genetreatment1 / 2completed
NCT04123626
A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Genetreatment1 / 2active_not_recruiting
NCT03913143
A Study to Evaluate Efficacy, Safety, Tolerability and Exposure After a Repeat-dose of Sepofarsen (QR-110) in LCA10 (ILLUMINATE)treatment2 / 3active_not_recruiting
NCT00001732
Screening for Studies on Inherited Eye DiseasesNo drug interventionsNot AvailableNot Availablecompleted
NCT00011817
Evaluation and Treatment of Patients With Inherited Eye DiseasesNo drug interventionsNot AvailableNot Availablecompleted