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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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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.