Bayer hat einen Antrag auf Verlängerung der Behandlungsintervalle von bis zu sechs Monaten mit Eylea® 8 mg (Aflibercept 8 mg, 114,3 mg/ml Injektionslösung) für die Behandlung der neovaskulären (feuchten) altersabhängigen Makuladegeneration (nAMD) und des diabetischen Makulaödems (DMÖ) bei der Europäischen Arzneimittel-Agentur (EMA) eingereicht / Der Antrag basiert auf den positiven Langzeitergebnissen aus den offenen Verlängerungsstudien der klinischen Studien PULSAR (bei nAMD) und PHOTON (bei DMÖ) über drei Jahre / 28% der Patienten bei DMÖ und 24% der Patienten bei nAMD hatten am Ende der drei Jahre ein letztes zugewiesenes Behandlungsintervall von 6 Monaten
Bayer hat bei der Europäischen Arzneimittel-Agentur (EMA)
Bayer hat bei der Europäischen Arzneimittel-Agentur (EMA)
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