Genetic sequencing for mutations causing inherited eye diseases in Texas (Texas 1000 Project) We are identifying disease-causing mutations using next-generation …
September 21, 2018
Genetic sequencing for mutations causing inherited eye diseases in Texas (Texas 1000 Project) We are identifying disease-causing mutations using next-generation …
Argus II Implant post-market study for retinitis pigmentosa (RP) We are conducting a five-year post-market study of Argus™ II retinal …
X-linked retinoschisis natural history studies We are enrolling qualified patients with x-linked retinoschisis in order to measure disease progression in …
Choroideremia natural history studies We are enrolling qualified patients with choroideremia in order to measure disease progression in a group …
Stargardt disease treatment trials Qualifying patients enter a treatment trial in an attempt to slow down or halt the progression …
August 28, 2018
Usher Syndrome Type IIA natural history study Usher Syndrome Type IIA (USH2A) is the most common form of combined hearing …
February 25, 2016
First-in-human trial of a new gene therapy that seeks to restore sight for patients affected with retinitis pigmentosa (Dallas, Texas …
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