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Ian C. Han, MD, shares his thoughts on the value of anecdotal evidence in our winter 2024 editorial.
Options empower patients and providers to decrease treatment burden
Clinical associations, imaging strategies and establishing a differential diagnosis from pseudopapilledema.
Boehringer Ingelheim announced that the phase 2 clinical studies will investigate a potential first-in-class oral compound and a highly specific antibody fragment for geographic atrophy.
The platform, developed by University College London and Heidelberg Engineering, demonstrated accuracy and precision in early tests.
Neovascular macular degeneration is multifactorial, which requires future agents to target multiple pathways.
The CNPV program was announced by the FDA in June 2025 and offers companies the opportunity to reduce standard application review times from 10–12 months to just 1–2 months.
Vitreoretinal SpecialistWestchester Medical CenterAssistant Professor, New York Medical CollegeValhalla, New York
Ferhina S. Ali, MD, discussed the real-world efficacy and durability of next-generation anti-VEGF agents like faricimab and aflibercept 8 mg, emphasizing how large-scale data offers insights into their performance and safety beyond clinical trials.
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