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Bayer startet Phase-III-Studie mit Aflibercept 8 mg beim retinalen Venenverschluss

(PresseBox) (Berlin, )
Die weltweite Phase-III-Studie QUASAR wird die Wirksamkeit und das Sicherheitsprofil von Aflibercept 8 mg bei Makulaödem infolge eines retinalen Netzhautvenenverschlusses untersuchen / Die Studie folgt auf positive Daten aus der Phase-III-Studie PULSAR bei neovaskulärer (feuchter) altersabhängiger Makuladegeneration (nAMD) und der Phase-II/III-Studie PHOTON beim diabetischen Makulaödem (DMÖ) / QUASAR wird voraussichtlich etwa 800 Patienten in 27 Ländern einschließen / Die Studie ergänzt das Entwicklungsprogramm für Aflibercept 8 mg und untersucht den Erhalt der Sehschärfe mit verlängerten Behandlungsintervallen bei weiteren Patientengruppen

Berlin, 10. Mai 2023 – Bayer startet die Phase-III-Studie QUASAR, in der die Wirksamkeit und das Sicherheitsprofil von Aflibercept 8 mg
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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.