Eylea HD (aflibercept) injection 8 mg approved by FDA for the treatment of macular oedema following retinal vein occlusion and for monthly dosing across approved indications

Regeneron Pharmaceuticals

19 November 2025 - Regeneron Pharmaceuticals today announced that the US FDA has approved Eylea HD (aflibercept) injection 8 mg for the treatment of patients with macular oedema following retinal vein occlusion with up to every 8 week dosing after an initial monthly dosing period. 

The FDA also approved an every 4 week (monthly) dosing option for some patients who may benefit from resuming this dosing schedule across approved indications: wet age-related macular degeneration, diabetic macular oedema, diabetic retinopathy and retinal vein occlusion.

Read Regeneron Pharmaceuticals press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , Registration