IMVIONIX debuts with acquisition of BEOVU's North American rights
Business

IMVIONIX debuts with acquisition of BEOVU's North American rights

Biotech company launches to commercial space; secures U.S. and Canadian exclusive rights to the FDA-approved injection for wet AMD and DME.
The Empire Forum debuts in NYC with full day of retina pipeline, industry, and investor talks
Events

The Empire Forum debuts in NYC with full day of retina pipeline, industry, and investor talks

Co-chairs Rishi Singh, MD, and David Eichenbaum, MD, led the inaugural meeting, which is set to return in 2027.
VeonGen on track for phase 3 Stargardt trial after FDA meeting
Pipeline

VeonGen on track for phase 3 Stargardt trial after FDA meeting

Phase 1/2 trial data demonstrate favorable safety profile and BCVA improvements; company has met with the FDA to plan the phase 3 program.
Scope launches OPTASE Heat Mask Pro for dry eye relief
Products

Scope launches OPTASE Heat Mask Pro for dry eye relief

New addition to the OPTASE product line of dry eye management solutions delivers targeted and symptomatic relief via Hydrobead moist heat technology.
Newton launches all-in-one OD program, refreshes Founders Optical brand
Business

Newton launches all-in-one OD program, refreshes Founders Optical brand

Newton Preferred program offers technology, lenses, frames, financing, and pricing in a single vision care program for independent practices.
Gout linked to worse diabetic retinopathy outcomes
Research

Gout linked to worse diabetic retinopathy outcomes

Patients with T2D and gout had higher DR risk, while urate-lowering therapy was associated with lower risks of some adverse outcomes.
Harrow debuts prescribing and access pharmacy platform
Business

Harrow debuts prescribing and access pharmacy platform

Company positions HarrowRx as a first-of-its-kind platform in the U.S. bringing prescribing, fulfillment, and patient support into one place for its entire branded portfolio.
FDA orders NAION risk added to GLP-1 RA warning labels
Products

FDA orders NAION risk added to GLP-1 RA warning labels

Federal agency issues new safety warning following new evidence; will now require all manufactures to update medication labels.
Cloudbreak Pharma releases positive phase 3 topline data on pterygium therapy
Pipeline

Cloudbreak Pharma releases positive phase 3 topline data on pterygium therapy

Data demonstrate durable reductions in pterygium vascularity with a favorable safety profile; company intends to review findings with FDA.
Eyedaptic launches AI visual assistant for smart glasses
Products

Eyedaptic launches AI visual assistant for smart glasses

Eva integrates with the E7 as a new category of intuitive and responsive assistive tech offering the ability to infer, reason, and take action in real time.
Prenatal opioid exposure tied to poorer vision, attention in kids
Research

Prenatal opioid exposure tied to poorer vision, attention in kids

Evidence also points to cognitive and educational difficulties that may become more apparent with age.
Glaukos and RevOpsis partner on retina tri-specific therapy development, commercialization
Pipeline

Glaukos and RevOpsis partner on retina tri-specific therapy development, commercialization

Exclusive licensing agreement also extends up to four retinal biologics.
Dexamethasone eye drops may cut invasive ROP treatment in preterm infants
Research

Dexamethasone eye drops may cut invasive ROP treatment in preterm infants

A 47% relative risk reduction fell short of statistical significance, but the safety data keep topical steroids in play as a noninvasive option.
Nacuity doses first patient in phase 3 trial on oral therapy for RP associated with Usher syndrome
Pipeline

Nacuity doses first patient in phase 3 trial on oral therapy for RP associated with Usher syndrome

Sites in the U.S. and Australia are actively enrolling patients for the SLO-RP Preserve trial.
Simple OCT rule helps cut glaucoma false positives in myopia
Research

Simple OCT rule helps cut glaucoma false positives in myopia

Expert-derived OCT interpretation rules offer a practical way to reduce false-positive glaucoma diagnoses in myopic eyes.
EyeDock debuts AI clinical assistant for ECPs
Products

EyeDock debuts AI clinical assistant for ECPs

Online clinical reference and toolkit now comes with a virtual assistant for answering questions from a curated database of contact lenses, medications, conditions, and codes.
Report: Rural residents face steep gap in retina care access
Research

Report: Rural residents face steep gap in retina care access

One in three rural Americans lives beyond an hour's drive of a retina specialist.
FDA grants Orphan Drug designation to Octant's RP oral therapy
Pipeline

FDA grants Orphan Drug designation to Octant's RP oral therapy

Oral small molecule is designed to correct protein misfolding for RHO gene mutations, the root cause of RHO-adRP; phase 1/2 clinical study currently underway.
Leadership watch: LENZ, CooperCompanies CEOs step down, among exec changes
Business

Leadership watch: LENZ, CooperCompanies CEOs step down, among exec changes

Leadership changes are underway in the eyecare space—and we’ve got the latest.
Roivant, Priovant report positive phase 3 NIU data for brepocitinib
Pipeline

Roivant, Priovant report positive phase 3 NIU data for brepocitinib

Oral therapy demonstrates broad and significant benefits in adults with NIU; companies target H1 2027 sBLA submission.