Automated vision-testing kiosks face concerns amid national expansion
Products

Automated vision-testing kiosks face concerns amid national expansion

With Eyebot’s 90-second vision tests rolling out across the country, the AOA is voicing words of caution over the self-administered kiosks.
CSI Dry Eye Innovations unveils new branding and software patent
Business

CSI Dry Eye Innovations unveils new branding and software patent

Rebrand paves way for potential future dry eye product launches to join its flagship, AI-based program: CSI Dry Eye Software.
Study demonstrates accuracy of new platform for comparing AI-based DR screening systems
Research

Study demonstrates accuracy of new platform for comparing AI-based DR screening systems

New testing platform allows for comparison of effectiveness and fairness in commercial AI systems.
FDA grants Fast Track designation for Drug Farm's ROSAH syndrome asset
Pipeline

FDA grants Fast Track designation for Drug Farm's ROSAH syndrome asset

S
Pseudoexfoliation glaucoma is most prevalent among Indigenous populations in the US
Research

Pseudoexfoliation glaucoma is most prevalent among Indigenous populations in the US

Study finds American Indian or Alaska Native patients are impacted by PXG and PG nearly threefold more than the general U.S. population.
FDA approves Tenpoint's YUVEZZI as first dual-agent presbyopia drop
Products

FDA approves Tenpoint's YUVEZZI as first dual-agent presbyopia drop

First and only combination drop of carbachol and brimonidine tartrate achieves miosis within 30 minutes and lasts up to 10 hours following once-daily dosing.
FDA approves Glaukos' iDose TR for repeat treatment labeling
Products

FDA approves Glaukos' iDose TR for repeat treatment labeling

Travoprost intracameral implant can now be re-administered using a repeat treatment protocol—enabling greater flexibility in glaucoma patient management.
Cannabis implicated in ocular inflammatory disease development
Research

Cannabis implicated in ocular inflammatory disease development

Cannabis use associated with higher risk of developing uveitis and other posterior segment diseases.
FDA approves Alembic's difluprednate 0.05% generic
Products

FDA approves Alembic's difluprednate 0.05% generic

Generic version of Sandoz’s Durezol is indicated for postop pain and inflammation as well as endogenous anterior uveitis.
Nidek launches Phantom Open-field Refraction System
Products

Nidek launches Phantom Open-field Refraction System

Device corrects refractive errors with virtual lenses simulating the same properties as real lenses—in under 5 minutes.
Conflicting evidence surrounds astigmatism's role in myopia
Research

Conflicting evidence surrounds astigmatism's role in myopia

Study highlights need for further investigation into the impact of astigmatism on myopia onset and progression.
FDA clears Novaliq's IND for NIAU phase 2 trial
Pipeline

FDA clears Novaliq's IND for NIAU phase 2 trial

Clearance enables FIH study of potentially the first steroid-free eye drop for controlling IOI among non-infectious anterior uveitis patients.
Novartis's ianalumab earns FDA Breakthrough Therapy designation for Sjögren’s disease
Pipeline

Novartis's ianalumab earns FDA Breakthrough Therapy designation for Sjögren’s disease

Fully human monoclonal antibody is delivered as a monthly subcutaneous injection; company plans to submit for global approval in early 2026.
OCuSOFT launches Retaine Omega Forte for dry eye
Products

OCuSOFT launches Retaine Omega Forte for dry eye

New nutritional supplement offers a daily dose of omega-3 essential fatty acids.
Leadership watch: Emmecell, ABO, Outlook, and Heidelberg make changes
Business

Leadership watch: Emmecell, ABO, Outlook, and Heidelberg make changes

Leadership changes are underway in the eyecare space—and we’ve got the latest.
FDA grants Orphan Drug designation to BlueRock's RP cell therapy
Pipeline

FDA grants Orphan Drug designation to BlueRock's RP cell therapy

Marks second designation for OpCT-001; includes tax credits for qualified clinical testing and, if approved, 7 years of U.S. market exclusivity.
New QLOSI safety data supports drop as pupil selective for presbyopia
Research

New QLOSI safety data supports drop as pupil selective for presbyopia

Head-to-head trial finds pilocarpine 0.4% resulted in no significant changes in ciliary muscle or lens thickness following dosing.
BioAge Labs expands into DME clinical program for oral inhibitor asset
Pipeline

BioAge Labs expands into DME clinical program for oral inhibitor asset

Preclinical evidence on NLRP3 inhibitor BGE-102 shows potential for therapeutic retinal exposure, with an initial POC trial to kick off later this year.
Registration now open for Eyes On Dry Eye 2026
Events

Registration now open for Eyes On Dry Eye 2026

Largest virtual dry eye event of the year offers up to 7 hours of free CE from leading clinical experts.
Could high HDL levels lead to lower DR risk?
Research

Could high HDL levels lead to lower DR risk?

Study emphasizes importance of monitoring HDL levels in patients with diabetic retinopathy.