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Bayer kündigt Phase-III-Studien mit neuer 8mg Aflibercept-Formulierung an

(PresseBox) (Berlin, )
Bayer und Regeneron Pharmaceuticals, Inc. planen zwei Phase-III-Studien mit den Bezeichnungen PHOTON und PULSAR. Die Studien untersuchen verlängerte Behandlungsintervalle mit einer neuen Aflibercept-Formulierung von 8mg zur intravitrealen Injektion. Die Zielgruppen sind Erwachsene mit Verschlechterung der Sehschärfe aufgrund eines diabetischen Makulaödems (DMÖ) und Erwachsene mit einer neovaskulären altersabhängigen Makuladegeneration (nAMD). Aflibercept 2mg ist bereits unter dem Markennamen Eylea® in mehr als 100 Ländern für fünf Indikationen zugelassen. Beide Studien sollen in diesem Jahr starten.

Die PHOTON- und PULSAR-Studien wurden bereits auf dem diesjährigen Kongress „Angiogenesis, Exudation and Degeneration“ in Miami, Florida, vorgestellt. Die multizentrischen, randomisierten, doppelblinden Studien untersuchen die Wirksamkeit und iyz Acdbkauqvbgfejfqv jik 2zg Vhuecydqznc jt Zlbbraskiprdfhqcdzp fgp 11 Rdduee (5 Fxjvdmr) hcj rzzjaf.

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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.