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Optics News
Study of atropine-based myopia treatment fails to meet primary efficacy endpoint
Eyenovia’s phase 3 CHAPERONE study evaluating low-dose atropine delivered via the company’s Optejet dispenser is not meeting its primary endpoint of a less than 0.50 D progression in visual acuity over 3 years, according to a press release.
The Latest News and Notes, plus Conversation with Tom Mitro
In this episode, John A. Hovanesian, MD, FACS, and Jim Mazzo discuss the latest news and trends and chat with Tom Mitro about his career and impact in ophthalmology.
Consistent research necessary to understand myopia as a disease
According to a new report from the National Academies of Sciences, Engineering and Medicine, more consistent international data are necessary to fully understand myopia and its underlying mechanisms.
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CureSight demonstrates greater visual acuity gains vs. patching in patients with amblyopia
Patients with amblyopia who were treated with the CureSight eye-tracking system achieved greater improvement in visual acuity at week 16 vs. those treated with patching, according to a study published in American Journal of Ophthalmology.
LENZ Therapeutics submits NDA for drops to treat presbyopia
LENZ Therapeutics has submitted a new drug application to the FDA for LNZ100, a preservative-free, once-daily aceclidine-based ophthalmic solution designed to treat presbyopia, the company announced in a press release.
Children with high myopia have greater foveal thickness in inner retina
The progression of myopia among school-aged children in China appeared to primarily affect changes in inner retinal thickness over the course of 1 year, according to research.
VIDEO: Study evaluates outcomes for optic pathway gliomas linked to neurofibromatosis type 1
PHILADELPHIA — In this video, Michael Fisher, MD, discusses the results of a natural history study he presented at the International Symposium on Pediatric Neuro-Oncology.
Real-world data show Luminopia improves visual acuity in children with amblyopia
Digital health company Luminopia Inc. announced real-world data from the Patients Using Prescription Luminopia Registry, which demonstrated the efficacy of its binocular, virtual reality-based medical device for children with amblyopia.
LFR-260 tele-refractor receives FDA clearance
The FDA cleared the LFR-260, a light field powered subjective tele-refractor, Evolution Optiks announced in a press release.
SightGlass receives FDA breakthrough designation for spectacle lenses that slow myopia
The FDA has granted breakthrough device designation to SightGlass Vision’s diffusion optics technology spectacle lenses, which are designed to slow myopia progression in children.
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