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Aflibercept 8 mg von Bayer zur Zulassung in der EU empfohlen

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Die Empfehlung durch den Ausschuss für Humanarzneimittel (CHMP) basiert auf den positiven Ergebnissen der klinischen Studien PULSAR bei neovaskulärer (feuchter) altersabhängiger Makuladegeneration (nAMD) und PHOTON beim diabetischen Makulaödem (DMÖ) / Nach Genehmigung der Zulassung durch die Europäische Kommission wird Aflibercept 8 mg das einzige Arzneimittel sein, das verlängerte Behandlungsintervalle von bis zu 5 Monaten bei Patienten mit nAMD und DMÖ ermöglicht / Diese Intervalle erzielte Aflibercept 8 mg bei vergleichbarem Wirksamkeits- und Sicherheitsprofil im Vergleich zum Therapiestandard Eylea® (Aflibercept 2 mg) / Die Entscheidung der Europäischen Kommission wird in den nächsten Monaten erwartet

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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.