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Eye Diseases, Hereditary

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Eye Diseases, Hereditary

Explore clinical trials studying Eye Diseases, Hereditary. Study availability and eligibility vary by location and protocol.

836 public trials 191 recruiting studies

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Eye Diseases, Hereditary trial results

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Study of EO2002 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction

NCT07729137

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Diseases, Corneal Dystrophies, Hereditary, +21 more
Locations: Clinical Site 1 Menlo Park, California, United States

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Haloperidol For Outpatient Symptom Management in Patients Diagnosed With Cannabinoid Hyperemesis Syndrome in the Emergrency Department

NCT07726069

Conditions: Albinism, Cannabinoid Hyperemesis Syndrome, Chediak-Higashi Syndrome, +15 more
Locations: University of Illinois Hospital Chicago, Illinois, United States

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A Phase III Study of KHN939 in Chinese Patients With Moderate-to-Severe Active Thyroid Eye Disease

NCT07720635

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University Shanghai, Shanghai Municipality, China

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A Phase III Study of KHN939 in Chinese Patients With Moderate-to-Severe Inactive Thyroid Eye Disease

NCT07720648

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University Shanghai, Shanghai Municipality, China

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A 24-Month Trial of NPI-001 for the Preservation of Photoreceptors in Retinitis Pigmentosa Associated With Usher Syndrome

NCT07710196

Conditions: Abnormalities, Multiple, Blindness, Congenital Abnormalities, +24 more
Locations: Not specified

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Safety and Tolerability of Subretinal OPGx-RDH12-1001 for LCA-Associated Inherited Retinal Degeneration (LCA-IRD)

NCT07681778

Conditions: Eye Diseases, Eye Diseases, Hereditary, Leber Congenital Amaurosis, +2 more
Locations: Associated Retina Consultants Phoenix, Arizona, United States

Perelman School of Medicine, University of Pennsylvania Philadelphia, Pennsylvania, United States

Retina Consultants of Texas & Retina Group Inc. Houston, Texas, United States

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24-Month Trial of NPI-001 for the Preservation of Photoreceptors in Retinitis Pigmentosa Associated With Usher Syndrome

NCT07290530

Conditions: Abnormalities, Multiple, Blindness, Congenital Abnormalities, +24 more
Locations: Not specified

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Open-Label Extension Study of MHB018A in Patients With Thyroid Eye Disease

NCT07620405

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Not specified

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Treatment of Chronic Thyroid Eye Disease With MHB018A

NCT07622121

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Not specified

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Treatment of Active Thyroid Eye Disease With MHB018A in a Randomized, Placebo-Controlled Study

NCT07622108

Conditions: Autoimmune Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, +12 more
Locations: Not specified

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Eye Diseases, Hereditary

Eye Diseases, Hereditary trial results

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