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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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