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Bayer AG Gebäude W 11 51368 Leverkusen, Germany http://www.bayer.de
Contact Ms Jutta Schulze +49 175 3002905
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Bayer AG

Aflibercept 8 mg erreicht primären Endpunkt in Phase-III-Studie und zeigt Visusgewinne mit verlängerten Behandlungsintervallen bei retinalem Venenverschluss

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Etwa 90 % der Patienten mit Aflibercept 8 mg wurde auf ein 8-wöchiges Behandlungsintervall eingestellt und behielt dieses Intervall bis zur Woche 36 bei / Aflibercept 8 mg zeigte eine schnelle und robuste Reduzierung der Flüssigkeit in der Netzhaut, gemessen an den Veränderungen der zentralen Makuladicke / Aflibercept 8 mg war gut verträglich und das Sicherheitsprofil entsprach dem aus früheren klinischen Studien / Detaillierte Ergebnisse werden bei Zulassungsbehörden weltweit eingereicht und auf bevorstehenden wissenschaftlichen Tagungen präsentiert

Bayer hat heute erste positive Ergebnisse der globalen Phase-III-Studie QUASAR bekannt gegeben, in der die Wirksamkeit und Sicherheit von Aflibercept 8 mg bei Patienten
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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.