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Genetic Study of Macular Degeneration Clinical Trial

Principal Investigator

Richard B. Rosen, M.D.

Enrollment Status:

Closed to Enrollment


To correlate the genotypic make-up with the disease phenotype in rare ophthalmic diseases. Genes and diseases currently being tested:

Aniridia, Axenfeld-Rieger Syndrome, Best Disease, Congential Cranial Dysinnervation Diseases (CCDD), Choroideremia, Cone Rod Dystrophy, Congenital Stationary Night Blindness, Corneal Anterior Stromal Dystrophies, Meesman's Epithelial Dystrophy, Bietti's Crystalline Corneal-Retinal Dystrophy, Soyne Honeycomb Dystrophy, Familial Exudative Vitreal Retinopathy, Glaucoma, Infantile Neuroaxonal Dystrophy (INAD), Optic Atrophy, Pattern Dystrophy, Pantothenate Kinase-associated Neuropathy (PKAN), Juvenile X-linked Retinoschisis, Retinitis Pigmentosa (RP) and Retinal Degenerations, Retinoblastoma, Sorsby Fundus Dystrophy, Stargardt Disease.


Please contact the study manager.

Contact Us

Dr. Richard Rosen, Principal InvestigatorTel: (212) 979-4284

Katy Tai, Research ManagerTel: (212) 979-4251

Address310 E. 14th StreetNew York, NY 10003

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