Harrow purchases US commercialization rights to Samsung Bioepis' biosimilar portfolio
Business

Harrow purchases US commercialization rights to Samsung Bioepis' biosimilar portfolio

Acquisition includes two major anti-VEGF therapies for retinal diseases: OPUVIZ and BYOOVIZ, generic equivalents to EYLEA and Lucentis, respectively.
FDA accepts Aldeyra's resubmitted reproxalap NDA
Pipeline

FDA accepts Aldeyra's resubmitted reproxalap NDA

Company hopes third submission of the DED application is the charm for achieving marketing approval by a Dec. 26, 2025 PDUFA date.
Lupin launches Lotemax generic suspension in the US
Products

Lupin launches Lotemax generic suspension in the US

Loteprednol etabonate ophthalmic suspension, 0.5%, is indicated to treat postoperative inflammation and pain following ocular surgery, among other conditions.
Octane's Ophthalmology Tech Forum highlights AI and personalized medicine
Events

Octane's Ophthalmology Tech Forum highlights AI and personalized medicine

Annual industry event saw ophthalmology industry leaders discussing what the future holds for AI-powered care.
Researchers develop infrared light-sensing contacts for humans
Research

Researchers develop infrared light-sensing contacts for humans

The lenses converted infrared light into visible light and performed better when participants closed their eyes.
Belite Bio concludes enrollment for phase 3 GA trial on oral tinlarebant
Pipeline

Belite Bio concludes enrollment for phase 3 GA trial on oral tinlarebant

Also under clinical development for Stargardt disease, the once-daily tablet is under evaluation for its efficacy in slowing atrophic lesion growth.
Pivotal study validates SCANLY Home OCT device for nAMD management
Research

Pivotal study validates SCANLY Home OCT device for nAMD management

New research further supports the clinical performance of Notal Vision's FDA-cleared, AI-based OCT monitoring system for at-home use.
FDA OKs AAVantgarde's IND for Stargardt gene therapy trial
Pipeline

FDA OKs AAVantgarde's IND for Stargardt gene therapy trial

Clearance enables initiation of FIH study on AAVB-039, an AAV8 that delivers the full-length ABCA4 gene to address the disease’s root cause—enabling treatment for all types.
Meta reportedly buys minority stake in EssilorLuxottica
Business

Meta reportedly buys minority stake in EssilorLuxottica

The estimated $3.51 billion investment follows companies’ recent plans to launch AI-powered smart glasses for the Oakley sports performance frames this summer.
New IRD genetic testing maps mutations to improve diagnoses
Research

New IRD genetic testing maps mutations to improve diagnoses

Newly identified gene variants may enhance speed and accuracy in diagnosing inherited retinal diseases.
Nanoscope begins rolling BLA submission for RP gene-agnostic therapy
Pipeline

Nanoscope begins rolling BLA submission for RP gene-agnostic therapy

With a full submission planned for early 2026, MC0-010 has the potential to become the first optogenetic therapy to restore vision in legally blind RP patients.
Optometry Divas to host celebratory 10-year anniversary events
Events

Optometry Divas to host celebratory 10-year anniversary events

Weekend-long celebration includes 2025 annual educational retreat with 16 CE credits up for grabs, along with an Optometry Giving Sight-partnered banquet fundraiser.
Leadership watch: ViaLase, J&J, Alcon, and myze make executive additions
Business

Leadership watch: ViaLase, J&J, Alcon, and myze make executive additions

Check out the latest leadership news from the eyecare space, including a new CEO at ViaLase and a leading optometrist joining myze.
Eyes On Glaucoma 2025 highlights advancements in disease care
Events

Eyes On Glaucoma 2025 highlights advancements in disease care

Largest virtual glaucoma meeting of the year sees record attendance.
FDA agrees to Atsena's regulatory pathway for XLRS gene therapy
Pipeline

FDA agrees to Atsena's regulatory pathway for XLRS gene therapy

Expansion of LIGHTHOUSE study will support potential BLA submission in early 2028 to become the first FDA-approved treatment for the inherited retinal disease.
 4DMT cuts 25% of workforce and fast-tracks wet AMD gene therapy program
Business

4DMT cuts 25% of workforce and fast-tracks wet AMD gene therapy program

Company reports streamlined planning to advance phase 3 clinical trials of 4D-150, under evaluation to deliver a single, low-dose, and sustained multi-year intravitreal injection.
LENZ and Théa partner on Canadian commercialization of presbyopia eye drop
Pipeline

LENZ and Théa partner on Canadian commercialization of presbyopia eye drop

Licensing and commercialization agreement gives LENZ $70 million in upfront and milestone payments; news comes as company awaits FDA approval.
Alcon to purchase LumiThera
Business

Alcon to purchase LumiThera

Targeting a Q3 sale, acquisition includes Valeda Light Delivery System, the first and only PBM treatment for early-to-intermediate dry AMD.
Eyenovia rebrands as Hyperion DeFi, Inc with new focus
Business

Eyenovia rebrands as Hyperion DeFi, Inc with new focus

Name change aligns with company's pivot toward decentralized finance and focus on a cryptocurrency treasury reserve strategy; plans remain to commercialize Optejet.
Vision Expo shifting to single annual event in 2026
Events

Vision Expo shifting to single annual event in 2026

Starting next February in Orlando, the trade-only conference and exhibition will rotate its location throughout major U.S. cities moving forward.