Bayer hat heute die Zulassung von der Europäischen Kommission für ein neues Behandlungsschema mit Eylea® erhalten. Dieses ermöglicht eine frühzeitige Verlängerung der Behandlungsintervalle bei Patienten mit neovaskulärer altersabhängier Makuladegeneration (nAMD) bereits im ersten Behandlungsjahr. Das neue Behandlungsschema erlaubt es den behandelnden Ärzten, die individuellen Behandlungsintervalle für die Patienten, abhängig von den funktionellen und/oder morphologischen Befunden auszudehnen.
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