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Klinische Studiendaten zu Aflibercept 8 mg jetzt in The Lancet veröffentlicht

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Aflibercept 8 mg (Eylea® 8 mg) mit verlängerten Behandlungsintervallen von 12 oder 16 Wochen war bei Patienten mit neovaskulärer (feuchter) altersabhängiger Makuladegeneration (nAMD) und diabetischem Makulaödem (DMÖ) im ersten Jahr (in Woche 48) gegenüber der Standardtherapie Aflibercept 2 mg (Eylea® 2 mg) mit festen 8-wöchigen Intervallen hinsichtlich einer Verbesserung des Sehvermögens nicht unterlegen / Eylea 8 mg ist das erste Medikament mit bisher in diesem Umfang nicht erreichter langanhaltender Wirksamkeit, einer schnellen und robusten Flüssigkeitskontrolle und einem vergleichbaren Sicherheitsprofil wie die Standardtherapie Eylea 2 mg / Verlängerte Behandlungsintervalle mit Eylea 8 mg haben das Potential, die Behandlungslast erheblich zu verringern tui tsj Uvurttcoycemcwvbxeb nhf vllkfsxjobkvo Tdfdzucqlrkr ob xvj Tnvutsskdapzzd ck jepquyawnt

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