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FDA approves expanded EYLEA HD dosing intervals
Regeneron Pharmaceuticals’ EYLEA HD (aflibercept) injection 8 mg has received expanded FDA approval for extended dosing intervals in wet age-related macular degeneration (AMD) and diabetic macular edema (DME). This allows for administration up to every 20 weeks following one year of successful response, building on previous approvals. The decision is based on 96-week data from the PULSAR and PHOTON trials, demonstrating sustained efficacy and safety with extended intervals.