Articles

  • 1 week ago | ophthalmologytimes.com | Dilraj S. Grewal |Sydney M Crago |Kassi Filkins

    Dilraj S. Grewal, MD, FASRS, an associate professor of ophthalmology at Duke Eye Center, spoke with Ophthalmology Times at the 2025 Retina World Congress meeting held in Fort Lauderdale, Florida. At this meeting, Grewal gave a presentation entitled, "New therapeutics for non-infectious uveitis in 2025," which provided an in-depth overview of the current state of research and treatment innovations. Note: This conversation has been lightly edited for clarity.

  • 1 week ago | ophthalmologytimes.com | Priya S. Vakharia |Sydney M Crago |Kassi Filkins

    Priya S. Vakharia, MD, a retina specialist at Retina Vitreous Associates of Florida in Tampa Bay, presented findings from the ARCHER trial investigating geographic atrophy (GA) treatment for dry age-related macular degeneration (AMD) during the 2025 Retina World Congress annual meeting. Note: The following conversation has been lightly edited for clarity. Ophthalmology Times: You presented on the ARCHER trial here at Retina World Congress. Can you give us a few highlights from this presentation?

  • 1 week ago | ophthalmologytimes.com | Sydney M Crago |Sunir J. Garg |Kassi Filkins

    Sunir Garg, MD, a professor of ophthalmology at Wills Eye Hospital and partner with Mid-Atlantic Retina, discussed with Ophthalmology Times one significant challenge in ophthalmological procedures: patient discomfort during intravitreal injections caused by povidone iodine. Note: The following conversation has been lightly edited for clarity. Ophthalmology Times: Can you share more about the the challenges behind current anti-sepsis options for intravitreal injections?

  • 1 month ago | europe.ophthalmologytimes.com | Kassi Filkins

    A pioneer of refractive laser eye surgery in the UK, Professor David Gartry, MD, FRCS, FRCOphth, FCOptom, reached the milestone in the 36th year of his career

  • 1 month ago | optometrytimes.com | Martin Harp |Hattie Hayes |Kassi Filkins

    April 21, 2025By The FDA did not agree with a supplemental Biologics License Application for the addition of extended dosing intervals of up to 24 weeks across currently-approved indications.

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