Orbital and preseptal cellulitis are on the rise in the US
Research

Orbital and preseptal cellulitis are on the rise in the US

Study finds the incidence rate of preseptal cellulitis has increased three-fold since 2006.
Opus Genetics reports first-in-human trial data on LCA gene therapy
Pipeline

Opus Genetics reports first-in-human trial data on LCA gene therapy

One-month findings from the first of three pediatric dosings indicate a clinically meaningful improvement in vision following just one dosing.
Do personality traits play a role in DED development?
Research

Do personality traits play a role in DED development?

New study links higher neuroticism, lower conscientiousness to increased odds of dry eye disease.
FDA grants ANDA approval to olopatadine hydrochloride for ocular allergy relief
Products

FDA grants ANDA approval to olopatadine hydrochloride for ocular allergy relief

Generic of Alcon’s Pataday Once Daily Relief is intended for use as an antihistamine to treat itchy eyes.
Opthea to cut workforce by an estimated 65%
Business

Opthea to cut workforce by an estimated 65%

Significant layoffs follow in wake of the company's phase 3 trial failures and subsequent termination of its wet AMD program late last month.
How will reciprocal tariffs impact the optical industry?
Business

How will reciprocal tariffs impact the optical industry?

The Vision Council updates industry members as the U.S. imposes new 10% tariffs on 60+ countries across the globe—and 125% on China.
FDA accepts Outlook Therapeutics' bevacizumab BLA for wet AMD
Pipeline

FDA accepts Outlook Therapeutics' bevacizumab BLA for wet AMD

With a PDUFA date of Aug. 27, ONS-5010 (LYTENAVA) could become the first FDA-approved bevacizumab formulation targeting this retinal disease.
Daily hour of screen time increases myopia risk by nearly 25%
Research

Daily hour of screen time increases myopia risk by nearly 25%

Investigators report significant increase in myopia risk seen with up to 4 hours of daily screen time, after which the risk rose more gradually.
Tenpoint submits NDA for Brimochol PF for presbyopia
Pipeline

Tenpoint submits NDA for Brimochol PF for presbyopia

The FDA begins a 60-day review period to determine if the submission for the pupil-modulating eye drop is acceptable.
 Avisi reports positive 6-month data on VisiPlate aqueous shunt for glaucoma
Pipeline

Avisi reports positive 6-month data on VisiPlate aqueous shunt for glaucoma

MIBS device composed of non-fibrotic nanotechnology-based metamaterials lowered OAG patients’ mean IOP by 40%.
Hormones may play key role in DR risk among diabetes patients
Research

Hormones may play key role in DR risk among diabetes patients

Surprising findings reveal how sex hormones may secretly influence the risk for diabetic retinopathy.
Orasis's QLOSI for presbyopia launches in the US
Products

Orasis's QLOSI for presbyopia launches in the US

Pilocarpine 0.4% provides patients with flexible dosing for up to 8 hours of clear near vision; prescription-based drops are available through two pharmacy partners.
New North Dakota bill establishes optometric telemedicine guidelines
Legal

New North Dakota bill establishes optometric telemedicine guidelines

Legislation prioritizes patient safety and increased access to standardized virtual care across the state.
Avulux migraine glasses added to federal pediatric medical device accelerator
Products

Avulux migraine glasses added to federal pediatric medical device accelerator

FDA-funded MedTech organization will provide resources to support unique precision lens tech, designed to block up to 87% of harmful and mitigate photophobia effects.
Lifestyle habits may benefit cognitive impairment in glaucoma
Research

Lifestyle habits may benefit cognitive impairment in glaucoma

Mindfulness meditation may help slow the rate of neurocognitive decline.
Hoya introduces VisuPro All Day and Flex lenses for young presbyopes
Products

Hoya introduces VisuPro All Day and Flex lenses for young presbyopes

Advanced spectacle lenses target adult patients experiencing an initial gradual loss of vision.
 FDA rejects Aldeyra's reproxalap NDA for a second time
Pipeline

FDA rejects Aldeyra's reproxalap NDA for a second time

Agency states the candidate failed to demonstrate efficacy in treating ocular symptoms associated with dry eyes; company plans for a third submission.
Alcon launches Clareon PanOptix Pro IOL in the US
Products

Alcon launches Clareon PanOptix Pro IOL in the US

With a broad commercial rollout planned for next month, this will be the company’s first presbyopia-correcting IOL available in its Clareon AutonoMe preloaded system.
OKYO's urcosimod demonstrates long-term stability for NCP
Pipeline

OKYO's urcosimod demonstrates long-term stability for NCP

With a real-world study ongoing, urcosimod’s +2.5-year shelf stability further supports a potential NDA submission for regulatory approval down the road.
Chronic stress linked to increased AMD risk
Research

Chronic stress linked to increased AMD risk

Study joins a growing body of evidence that chronic stress is an important risk factor for ocular diseases.