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Bayer AG Gebäude W 11 51368 Leverkusen, Germany http://www.bayer.de
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Bayer AG

Aflibercept 8 mg erster Wirkstoff mit verlängerten Injektionsintervallen von 16 Wochen bei bis zu 89 Prozent der Patienten

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In zwei internationalen zulassungsrelevanten Studien erreicht Aflibercept 8 mg jeweils den primären Endpunkt auf Nicht-Unterlegenheit bei neovaskulärer (feuchter) altersbedingter Makuladegeneration (nAMD) und diabetischem Makulaödem (DMÖ) in Bezug auf die Veränderung der bestkorrigierten Sehschärfe versus Eylea® (Aflibercept 2 mg) nach 48 Wochen / Lang anhaltende Wirksamkeit bei nAMD und DMÖ: 77 % der nAMD- und 89 % der DMÖ-Patienten behielten 16-wöchiges Dosierungsintervall mit nur 5 Injektionen im ersten Jahr bei / Aflibercept 8 mg zeigt vergleichbares Sicherheitsprofil wie etabliertes Sicherheitsprofil von Eylea / Bayer wird Daten bei Gesundheitsbehörden außerhalb der USA einreichen

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