Langzeitergebnisse und Subgruppenanalysen belegen eine langanhaltende Wirksamkeit und konsistente Sicherheit von intravitrealem Eylea® 8 mg (Aflibercept 8 mg) mit verlängerten Behandlungsintervallen für die Behandlung von Patienten mit neovaskulärer (feuchter) altersabhängiger Makuladegeneration (nAMD) und diabetischem Makulaödem (DME)
Insgesamt werden 14 Abstracts zu Eylea 8 mg und Eylea® 2 mg (Aflibercept 2 mg) vorgestellt
Bayer gab heute bekannt, dass neue Langzeitergebnisse und Subgruppenanalysen aus dem zulassungsrelevanten klinischen Studienprogramm für Aflibercept 8 mg (Eylea® 8 mg) für die neovaskuläre (feuchte) altersabhängige Makuladegeneration (nAMD) und das diabetische Makulaödem (DMÖ) auf der Jahrestagung der Association for Research in Vision and Ophthalmology (arvo.org), in Seattle, Washington, 5.-9. Pec 8320, xfgkhoseovh fibjpr.
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