August 27, 2026
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DENVER — Two studies presented at the Association for Research in Vision and Ophthalmology meeting explored the benefits of ATSN-101 for Leber congenital amaurosis and ATSN-201 for X-linked retinoschisis. In July, Atsena Therapeutics received orphan drug designation for the two gene therapy candidates from the European Medicines Agency, according to a press release.
August 27, 2026
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DENVER — A gene therapy showed “encouraging visual function improvements” in patients with Usher syndrome type 1B, according to a…

In this video interview, Sunir J. Garg, MD, FACS, FASRS, discussed 2-year results of the phase 2 LUNA study on ixoberogene…

A one-time injection of ABBV-RGX-314, a gene therapy for wet age-related macular degeneration, yielded reductions in treatment…

MONTREAL — In a phase 2b study, an intravitreal gene therapy reduced the treatment burden in patients with neovascular…

DENVER — MCO-010, an optogenetic therapy, demonstrated vision improvements for patients with retinitis pigmentosa at 3 years,…

Genethon’s Recent Accomplishments Underscore the Progress of Genetic Medicine from Scientific Promise to Clinical RealityRead…