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This partnership unites two leading eye health organizations to restore sight and transform millions of lives.
The breakthrough treatment, developed over 25 years, has already helped restore vision for some patients.
Three 2026 Breakthrough Prize winners reflect on developing Luxturna, a gene therapy that treats blindness caused by rare inherited eye diseases
Doctors at Duke Health are using a cell-based implant to slow down the progression of MacTel, a rare retinal disease that damages light-sensitive cells in the back of the eye, caus...
Restore Vision, a company developing gene therapy drugs to regenerate vision lost due to retinal diseases, announced on the 15th that it has raised ¥1.3 billion in a Pre-Series B r...
Critical Path Institute Awards $249,719 Grant to Odylia Therapeutics for Groundbreaking Gene Therapy Targeting Usher Syndrome Type 1C Vision Loss In an ambitious effort to combat a...
A 6-year-old girl in the UK is able to see normally again in the day and night thanks to a one-time gene therapy for a rare form of congenital blindness. At this very tender age, S...
In a groundbreaking study published in Cell Death Discovery, researchers led by Chien, JY., Woon, P.Y., and Tsai, HY. have illuminated a previously uncharted pathway in retinal deg...
Saffie's mum says Luxturna therapy at Great Ormond Street has been like "someone waved a magic wand".
Disrupting the eye’s internal limiting membrane enables transplanted stem cell–derived retinal ganglion cells to survive, migrate, and form connections, offering a potential future...
THURSDAY, April 23, 2026 — A new gene therapy to treat inherited deafness produces a lasting cure, a new international study has found. The treatment, which targets the OTOF gene,...
A nanosized extract of the plant thylakoid grana — the molecular engine behind photosynthesis — is transplanted into the eye's corneal cells, producing a key protective molecule wh...
A group of pediatric eye disease researchers has launched an open-access tool designed to help manage pediatric cases of amblyopia, a condition in which the brain fails to properly...
The organisers said the campaign is expected to benefit residents from Arusha and surrounding regions, where visual impairment remains among the leading causes of disability.
Rund 76 Millionen Menschen weltweit sind am Grünen Star erkrankt. Forschende der Medizinischen Hochschule Hannover entwickeln derzeit ein individuell steuerbares Implantat für Glau...
A married couple of scientists who met as students at Harvard has won the 2026 Breakthrough Prize in Life Sciences for creating the world's first gene therapy to restore sight in p...
Learn about a new map of the human eye made using donated eyeballs that could help explain and possibly prevent a handful of sight-related diseases.
A new tool that tethers healthy mitochondria to ailing cells has shown promise in mice with inherited blindness. The post Scientists Revive Failing Cells With Mitochondria Transpla...
Regeneration has long been the stuff of science fiction. At UNLV, researchers are now studying frogs that can regrow their eyes in days — work that could bring that idea closer to...
The drops, tested on mice, healed eye damage using light-sensitive particles—sourced from ordinary spinach. The post Photosynthetic Drops Soothe Dry Eyes With Sunlight appeared fir...
Prevent Blindness to host four 2026 webinars engaging allies and advocates to improve access to vision and eye care.
The VCF is working closely with the IAPB, a founding partner of the VCF, alongside leading international eye health organizations.
Scientists at UC Irvine have found a way to potentially reverse age-related vision loss by targeting the ELOVL2 “aging gene” and restoring vital fatty acids in the retina. Their ex...
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