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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

Bayer beantragt Zulassung in der EU für 6-monatiges Behandlungsintervall mit Eylea® 8 mg

(PresseBox) (Leverkusen, )
Bayer hat einen Antrag auf Verlängerung der Behandlungsintervalle von bis zu sechs Monaten mit Eylea® 8 mg (Aflibercept 8 mg, 114,3 mg/ml Injektionslösung) für die Behandlung der neovaskulären (feuchten) altersabhängigen Makuladegeneration (nAMD) und des diabetischen Makulaödems (DMÖ) bei der Europäischen Arzneimittel-Agentur (EMA) eingereicht / Der Antrag basiert auf den positiven Langzeitergebnissen aus den offenen Verlängerungsstudien der klinischen Studien PULSAR (bei nAMD) und PHOTON (bei DMÖ) über drei Jahre / 28% der Patienten bei DMÖ und 24% der Patienten bei nAMD hatten am Ende der drei Jahre ein letztes zugewiesenes Behandlungsintervall von 6 Monaten

Bayer hat bei der Europäischen Arzneimittel-Agentur (EMA)
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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.