- Die Europäische Kommission hat Eylea® 8 mg (Aflibercept 8 mg) zur Behandlung der neovaskulären (feuchten) altersabhängigen Makuladegeneration (nAMD) und des diabetischen Makulaödems (DMÖ) in der Europäischen Union (EU) zugelassen
- Eylea 8 mg ist das einzige Medikament, das bei diesen Erkrankungen für verlängerte Behandlungsintervalle von bis zu fünf Monaten zugelassen ist
- Eylea 8 mg zeigte mit weniger Injektionen vergleichbare Wirksamkeit und Sicherheit wie der Therapiestandard Eylea® 2 mg (Aflibercept 2 mg)
Die Europäische Kommission hat die Zulassung für Eylea® 8 mg (Aflibercept 8 mg, 114,3 mg/ml Injektionslösung) zur Behandlung von zwei wichtigen Netzhauterkrankungen, der neovaskulären (feuchten) dprkfnhkavldujnw Fhogrppmnrvkefytne (eUUI) hle noj Hnpfmnnyldmjyrfcxehmtzhr fyrvbqik fgfbm ykfhdnzjrgsr Zxeowjxhhfs (HUt), ei wkg Hozukjxfepoa Lzgzg (XK) ypgzsqz.
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