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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Real-World Study to Gain Clinical Insights Into Roche Ophthalmology ProductsBranch Vein Occlusion, Embolism and Thrombosis, Venous Thrombosis, cardiovascular disorder, central retinal vein occlusion, diabetic macular edema, eye disorder, retinal disorder, retinal vein occlusion, thrombotic disease, vascular disorderActive, not recruitingNot stated2026-10-02NCT05476926
A Study to Test Whether BI 1815368 Helps People With an Eye Condition Called Diabetic Macular Edemaeye disorder, macular degeneration, macular retinal edema, retinal degeneration, retinal disorderRecruitingPhase 22026-10-01NCT06962839
A Study to Test Whether BI 764524 Helps People With an Eye Condition Called Diabetic RetinopathyDiabetes Complications, cardiovascular disorder, diabetes mellitus, diabetic peripheral angiopathy, diabetic retinopathy, endocrine system disorder, eye disorder, retinal disorder, vascular disorderActive, not recruitingPhase 22026-10-01NCT06321302
A Follow-on Study for Second-Eye Treatment for Participants Previously Treated With Gene Therapy for X-Linked Retinitis Pigmentosa (XLRP)X-Linked Retinitis PigmentosaActive, not recruitingPhase 22026-09-25NCT06646289
Follow-up Gene Therapy Trial for the Treatment of X-linked Retinitis Pigmentosa Associated With Variants in the RPGR GeneX-Linked Retinitis PigmentosaActive, not recruitingPhase 32026-09-25NCT04794101
Vitrectomy, Subretinal Tissue Plasminogen Activator (TPA) and Intravitreal Gas for Submacular Haemorrhage Secondary to Exudative (Wet) Age-related Macular Degeneration (TIGER).eye disorder, macular degeneration, retinal degeneration, retinal disorder, wet macular degenerationRecruitingPhase 32026-09-11NCT04663750
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic VariantsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaRecruitingNot stated2026-09-08NCT05589714
First-in-Human, Dose Escalation Trial of AXV-101 in BBS1-Related Retinal DegenerationBardet-Biedl syndrome 1, Eye Diseases, Hereditary, eye disorder, retinal degeneration, retinal disorderRecruitingEarly phase 12026-08-04NCT07269665
A Clinical Trial Evaluating the Safety and Efficacy of a Single Subretinal Injection of AGTC-501 in Participants With XLRPEye Diseases, Hereditary, eye disorder, retinal degeneration, retinal disorderActive, not recruitingPhase 2 / Phase 32026-04-07NCT04850118
Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1FCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, autosomal recessive nonsyndromic hearing loss 23, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaActive, not recruitingNot stated2026-02-04NCT04765345
Study of Serine Supplementation to Protect Vision in MacTelMacular Telangiectasia Type 2 (MacTel)Not yet recruitingPhase 32026-01-15NCT07342439
Investigating Geographic Atrophy Insights (i-GAIN) Natural History StudyEye Diseases, Hereditary, Geographic Atrophy, Skin Abnormalities, Skin and Connective Tissue Diseases, connective tissue disorder, eye disorder, macular degeneration, primary anetoderma, retinal degeneration, retinal disorder, skin disorderActive, not recruitingNot stated2025-06-13NCT05797896
Deciphering AMD by Deep Phenotyping and Machine Learning- Prospective Study - SUMMIT (Part 2)age-related macular degeneration, eye disorder, macular degeneration, retinal degeneration, retinal disorderEnrolling by invitationNot stated2024-11-12NCT06682455
Deciphering AMD by Deep Phenotyping and Machine Learning- Prospective Study - PINNACLEage-related macular degeneration, eye disorder, macular degeneration, retinal degeneration, retinal disorderActive, not recruitingNot stated2024-11-12NCT04269304