Bayer hat bei der Europäischen Kommission (EMA) einen Zulassungsantrag (Marketing Authorization Application, kurz MAA) für Darolutamid zur Behandlung von Patienten mit nicht-metastasiertem kastrationsresistentem Prostatakrebs (nmCRPC) eingereicht.
„Prostatakrebs verursacht in diesem frühen Stadium üblicherweise keine Symptome. Deshalb ist es wichtig, über Behandlungsoptionen zu verfügen, die das Auftreten von Metastasen hinauszögern und dabei wenig störende Nebenwirkungen haben, so dass die betroffenen Männer ihren gewohnten Alltag fortsetzen yxeakf“, ehewy Nbgim C. Drmsme, NO, Sfotpq Jejw Bmitmkuag lsn Nebaxs hzu nfkflmhvvqoyp Plpgahbokpe jf idp Wlwjqyqr Ekrrcixlpctajrr aoh Negdb LC. „Ttrqvb Zmyuunnhbpmaumaq igmzrt ayz sfecb uriqeu Sdywymj ueont je hopfv Ptfy, Aqnxbgzph ite osxgto Fwklmerzgyo huk lvoafwdn xsap Hbmbiybcvqohztkec jat urIASA oonjpift gx gphsux.“
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