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Gene Therapy Breakthrough Targets Vision Loss

RAI Radio 3 Rome 14d14d Impact 8

A Phase 1 clinical study has reported success in treating patients with near-total blindness. Patients were able to begin reading letters on an optotype chart. The study results were also featured in a Guardian profile of Jean Bennett, Catherine Eyre, and Albert McGuire. The research focused on patients who previously could not see anything. One early patient reported being able to see their child's face and delicate veins for the first time. The therapy has been in use since the publication of its first experimental results in 2008. The source noted the treatment's effectiveness has been widely reported. Patients have shown improvement in their ability to see objects from a distance following gene therapy treatment. The Loxturna gene therapy has won the Breakthrough Prize for treating Weber congenital amaurosis.

A Phase 1 clinical study has reported success in treating patients with near-total blindness. Patients were able to begin reading letters on an optotype chart. The study results were also featured in a Guardian profile of Jean Bennett, Catherine Eyre, and Albert McGuire. The research focused on patients who previously could not see anything. One early patient reported being able to see their child's face and delicate veins for the first time. The therapy has been in use since the publication of its first experimental results in 2008. The source noted the treatment's effectiveness has been widely reported. Patients have shown improvement in their ability to see objects from a distance following gene therapy treatment. The Loxturna gene therapy has won the Breakthrough Prize for treating Weber congenital amaurosis. Researchers suggest the therapy could potentially be applied to treating macularopathy or optic nerve trauma and compression. The discovery is being discussed as a advancement in ocular medicine.

Topics

vision restoration clinical trials ophthalmology

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Sources · 7 independent

RAI Radio 3

“uno studio di fase 1, quindi c'era molta preoccupazione anche per eventuali. che qualcosa si muoveva a livello dei loro occhi, erano pazienti che praticamente quasi ciechi, non vedevano niente, e cominciavano a leggere le prime lettere dell'ottotipo”

RAI Radio 3

“dal 2008, quando è stato pubblicato l'articolo del relativo, appunto la prima sperimentazione di questa terapia genica che avete chiamato Lux Turn... Andata molto, molto bene.”

RAI Radio 3

“Dal 2019 abbiamo trattato 30 pazienti, 30 pazienti che rappresentano la casistica più grande d'Europa in un singolo centro... I risultati sono stati molto positivi nel senso che i pazienti hanno migliorato la loro capacità visiva da lontano.”

RAI Radio 3

“senso che i pazienti hanno migliorato la loro capacità visiva da lontano.”

RAI Radio 3

“i pazienti hanno migliorato la loro capacità visiva da lontano. del campo vissivo e di miglioramento della nictalopia che è questa incapacità di vedere in codizioni scarse a luce”

RAI Radio 3

“questa scoperta, prima o poi per analogia potrebbe avere delle ricadute anche nella cura della maculopatia o su una amaurosi del trauma e compressione del nervo ottico.”

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