Eylea 8 mg with extended 6 month treatment interval approved in the EU

Bayer

27 June 2025 - The European Commission has granted a label extension in the EU for Eylea 8 mg (aflibercept 8 mg, 114.3 mg/ml solution for injection) with extended treatment intervals of up to 6 months for the treatment of two major retinal diseases, neovascular (wet) age-related macular degeneration (nAMD) and visual impairment due to diabetic macular oedema (DME). 

Eylea 8 mg is the first and only anti-vascular endothelial growth factor treatment in the EU with treatment intervals of up to 6 months for both patients with nAMD and DME.

Read Bayer press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , Europe , Registration