Prognia
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🇪🇺EU · EMAAuthorisedATC: S01LA05

Eyluxvi(aflibercept)

Wet Macular Degeneration;Macular Edema;Diabetes Complications;Retinal Vein Occlusion

Marketing Authorisation Holder: Biolitec pharma Limited Zweigniederlassung Jena

EMA Authorisation: 15/09/2025

INN: aflibercept

Indication

Eyluxvi is indicated for adults for the treatment of- neovascular (wet) age-related macular degeneration (AMD) (see section 5.1),- visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO) (see section 5.1),- visual impairment due to diabetic macular oedema (DME) (see section 5.1),- visual impairment due to myopic choroidal neovascularisation (myopic CNV) (see section 5.1). 

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.