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FDA will Alpharadin(TM) zur Behandlung des Prostatakarzinoms im vereinfachten Verfahren prüfen

"Fast Track"-Status für Krebsmedikament

(PresseBox) (Berlin, )
Die US-amerikanische Gesundheitsbehörde Food and Drug Administration (FDA) will AlpharadinTM (Radium-223-Chlorid), ein Entwicklungskandidat von Bayer und Algeta ASA, Oslo/Norwegen, in einem vereinfachten Verfahren ("Fast Track") prüfen. Das Mittel wird entwickelt für die Behandlung von Patienten mit kastrationsresistentem (hormonresistentem) Prostatakarzinom (CRPC), bei denen bereits Metastasen in den Knochen aufgetreten sind.

"Weltweit ist Prostatakrebs eine der häufigsten Todesursachen bei Männern. Besonders Patienten im fortgeschrittenen Stadium der Erkrankung, deren Krebs schon Tochtergeschwülste in den Knochen gebildet hat, benötigen dringend neue Behandlungsoptionen", sagte Dr. Kemal Malik, Leiter der Globalen Entwicklung und Mitglied des Bayer HealthCare Executive Committee. "Die Entscheidung der FDA, Alpharadin im 'Fast Vkckc'-Iurnmtfux xm jbrnru, ujj qrbax kgt eceqq Lvwdpkjblchsady ywr vbhhronaho Skvfyxvfm."

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