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Darolutamid erreicht primären Endpunkt in Phase-III-Studie ARANOTE bei Patienten mit metastasiertem hormonsensitivem Prostatakrebs

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ARANOTE-Studie erreicht den primären Endpunkt und verlängert signifikant das radiologische progressionsfreie Überleben (rPFS) mit Darolutamid plus Androgendeprivationstherapie (ADT) im Vergleich zu Placebo plus ADT / Die Sicherheitsanalyse zeigt, dass Darolutamid plus ADT mit Placebo plus ADT vergleichbar ist, und bestätigt damit das etablierte Verträglichkeitsprofil von Darolutamid, das in den Studien ARAMIS und ARASENS beobachtet wurde / Darolutamid plus ADT nun mit positiven Ergebnissen in zwei Phase III Zulassungsstudien im metastasierten hormonsensitiven Prostatakrebs (mHSPC) - sowohl mit als auch ohne Docetaxel / Bayer plant, die detaillierten Daten auf einem bevorstehenden wissenschaftlichen Kongress zu präsentieren und die Einreichung einer Zulassungserweiterung bei den
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