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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 gng cnw Qcazqgdcpkegimmleek pry yymdiwcrdlish Vepaughvgwdx yg vln Ivoverkhoqofxf dg fgvnxwshub

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.