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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Prescreening Study to Identify Potential Stargardt Participants for ACDN-01 Clinical Trials (STARPATH)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Juvenile Macular Degeneration, Stargardt Disease 1, Stargardt disease, cone-rod dystrophy, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, retinal degeneration, retinal disorderRecruitingNot stated2026-10-09NCT06445322
Suprachoroidal Administration in Subjects With Metastases to the ChoroidNeoplasms by Site, eye disorder, neoplasm, ocular cancerRecruitingPhase 22026-10-08NCT06643884
An Efficacy and Safety Study of Cenegermin Ophthalmic Solution Compared With Vehicle in the Treatment of PCEDConjunctival Diseases, Conjunctivitis, Allergic, Hypersensitivity, Immediate, conjunctivitis, eye disorder, immune system disorderRecruitingPhase 32026-10-07NCT07519902
Study to Evaluate ACDN-01 in ABCA4-related Stargardt Retinopathy (STELLAR)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Juvenile Macular Degeneration, Stargardt Disease 1, Stargardt disease, cone-rod dystrophy, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 1 / Phase 22026-10-07NCT06467344
ATSN-201 Gene Therapy in RS1-Associated X-linked Retinoschisiseye disorder, retinal degeneration, retinal disorder, retinoschisisRecruitingPhase 32026-09-29NCT05878860
ExCrossV Multi Site Trial for Vascularized High Risk KeratoplastyCorneal Transplant FailureRecruitingPhase 22026-09-21NCT06753916
Subconjunctival Humira for Boston KeratoprosthesisChemically-Induced Disorders, Conjunctival Diseases, Drug Eruptions, Drug-Related Side Effects and Adverse Reactions, Erythema, Hypersensitivity, Delayed, Pemphigoid, Benign Mucous Membrane, Skin and Connective Tissue Diseases, Stevens-Johnson syndrome, Stomatognathic Diseases, dermatitis, drug allergy, erythema multiforme, eye disorder, immune system disorder, mouth disorder, ocular cicatricial pemphigoid, skin disorder, stomatitis, vesiculobullous skin diseaseNot yet recruitingPhase 12026-08-31NCT06926478
An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Chronic Thyroid Eye Disease (TED)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Graves Ophthalmopathy, Graves disease, autoimmune disease, disease of orbital part of eye adnexa, endocrine system disorder, exophthalmos, eye disorder, goiter, hereditary disease, hyperthyroidism, immune system disorder, thyroid gland disorderActive, not recruitingPhase 32026-08-18NCT06625398
Clarifying the Optimal Application of SLT Therapy Trialeye disorder, glaucoma, ocular hypertensionRecruitingPhase 32026-08-14NCT04967989
A Phase 3 Randomized, Masked, Controlled Trial to Evaluate Efficacy and Safety of Belzupacap Sarotalocan (AU-011) Treatment Compared to Sham Control in Subjects With Primary Indeterminate Lesions or Small Choroidal MelanomaNeoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Uveal Neoplasms, eye disorder, malignant choroid melanoma, melanocytic neoplasm, melanoma, neoplasm, neuroendocrine neoplasm, ocular cancer, primitive neuroectodermal tumor, uveal disorder, uveal melanomaActive, not recruitingPhase 32026-07-31NCT06007690
Rate of Progression in USH2A-related Retinal DegenerationUsher syndrome type 2A, retinitis pigmentosa 39Active, not recruitingNot stated2026-07-23NCT03146078
Glaucoma Drainage Device and Endothelial Cell Loss Compare Trialeye disorder, glaucoma, ocular hypertensionRecruitingNot applicable2026-07-14NCT05924477
Study to Evaluate Ultevursen in Subjects With Retinitis Pigmentosa (RP) Due to Mutations in Exon 13 of the USH2A GeneAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Abnormalities, Eye Diseases, Hereditary, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Usher syndrome, Usher syndrome type 2, blindness (disorder), eye disorder, hearing disorder, hearing loss disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorderActive, not recruitingPhase 22026-07-09NCT06627179
Extended-release Sodium Oxybate (Lumryz) in Spasmodic Dysphonia and Voice TremorNeurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, laryngeal disorder, nervous system disorder, otorhinolaryngologic disease, respiratory system disorder, spasmodic dystonia, voice disordersNot yet recruitingPhase 12026-04-28NCT07041203
A Study to Investigate the Safety of DSP-3077 After a Unilateral Eye Injection in Male and Female Participants 18 Years of Age or Older With Retinitis PigmentosaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaRecruitingPhase 1 / Phase 22026-04-17NCT06891885
ctDNA in Cutaneous Squamous Cell CarcinomaNeoplasm, Residual, Neoplasms by Site, Neoplastic Processes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, neoplasm, skin disorder, skin neoplasm, skin squamous cell carcinomaRecruitingNot stated2026-03-30NCT06875609
A Trial of Hydrus Microstent Versus Goniotomyeye disorder, glaucoma, ocular hypertension, open-angle glaucomaRecruitingNot applicable2026-03-30NCT06289491
Study of Aspirin in Patients With Vestibular SchwannomaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Ear Diseases, NF2-related schwannomatosis, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Otorhinolaryngologic Neoplasms, acoustic neuroma, cranial nerve neoplasm, cranial nerve neuropathy, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neuroendocrine neoplasm, neurofibroma, neurofibromatosis, neuroma, otorhinolaryngologic disease, peripheral nervous system neoplasm, primitive neuroectodermal tumor, retrocochlear disease, schwannoma, vestibulocochlear nerve disorderActive, not recruitingPhase 22025-12-18NCT03079999
Brain Networks in DystoniaDyskinesias, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, basal ganglia disorder, blepharospasm-oromandibular dystonia syndrome, brain disorder, central nervous system disorder, craniofacial dystonia, dystonic disorder, focal hand dystonia, laryngeal disorder, movement disorder, nervous system disorder, otorhinolaryngologic disease, respiratory system disorder, spasmodic dystonia, voice disordersRecruitingNot stated2025-12-08NCT03042962
Study to Assess the Efficacy & Safety of KHK4951 in Patients With Neovascular Age-Related Macular DegenerationNeovascular Age-Related Macular Degeneration (nAMD)Active, not recruitingPhase 22025-10-30NCT06116890
Measurable Residual Disease Detection Using Tumor-Informed ctDNA Surveillance After Curative-Intent Treatment in HPV-Independent Squamous Cell Carcinoma of the Head and NeckHead and Neck Neoplasms, Neoplasms by Histologic Type, Neoplasms by Site, carcinoma, epithelial neoplasm, head and neck squamous cell carcinoma, neoplasm, squamous cell carcinomaRecruitingNot stated2025-05-18NCT06744296