The FDA accepted Aldeyra's resubmitted NDA for reproxalap after previous rejections due to efficacy concerns, despite no ...

The US Food and Drug Administration (FDA) recently granted fast track designation to Sanofi’s SAR446597 for the treatment of geographic atrophy (GA). 1 ...

A Chinese study reveals that secondhand smoke exposure significantly increases the risk of early-onset myopia in children ...

Presentation highlights include 48-month data from the OAKS and DERBY trials as well as the GALE open-label extension.

Krystal Biotech announced the first patient has been dosed in EMERALD-1, its phase 1/2 clinical trial evaluating KB801 for ...

To mark Ophthalmology Times' 50th anniversary, we invited top experts to reflect on the most significant innovations in ...

Alcon’s Voyager is a fully automated, noncontact treatment approach that delivers 120 laser pulses through the limbus of the ...

The tool is designed to help with the application of mono-dose, dry eye eyedrop vials more easily and accurately.

Nanoscope’s BLA has been granted rolling review by the FDA, with the first modules already submitted. The completion of the ...

The survey shows the evolving landscape of nAMD and DME treatments, highlighting physician preferences, payer influences, and ...

KAIST developed a microbial strain for efficient lutein production, offering an eco-friendly alternative to traditional ...

Alcon's Clareon Panoptix Pro IOL enhances cataract surgery with advanced light utilization and low visual disturbance.