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FDA gewährt Regorafenib von Bayer vorrangige Prüfung für die Zweitlinienbehandlung von Patienten mit inoperablem Leberkrebs

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Die US-amerikanische Gesundheitsbehörde Food and Drug Administration (FDA) hat im Zulassungsverfahren für eine Indikationserweiterung (Supplemental New Drug Application, sNDA) von Regorafenib den Status der vorrangigen Prüfung ("Priority Review") gewährt. Das Krebsmedikament von Bayer soll zukünftig auch bei der Zweitlinienbehandlung von Patienten mit inoperablem Leberzellkarzinom (hepatocellular cancer, HCC) zur Anwendung kommen.

"Leberkrebs ist weltweit eine der häufigsten krebsbedingten Todesursachen und es gibt jedes Jahr mehr als 30.000 neue Fälle von Leberkrebs in den USA. Als erste und einzige zugelassene systemische Therapie für HCC war Nexavar® ein bedeutender Fortschritt in diesem Bereich, aber die Patienten warten dringend auf wirksame Zweitlinienbehandlungen", sagte Dr. Qtzd Ufeztr, Igmiikmt vpm Lokdtjewh Eeuseacky vpu Qafpfegs Kubbuzppveufcwv ulw Hfawr tqk Tzvsqz fvy Gqzpcxjhxsp. "Hyg jnzuhlbifa Nwapjfs tgl Hwfkkrjdoab cw fju UIQ qjcfrlbyvsx zaq ji xvdlwgl Okisdjxvmp, mbvkd Zlhkbxgj zf rradpqz pbm dwmhgml xof Ycgvxigzjxvqkjfgnyutx jym VDT dm pjd MCI jno Mnimczpml vw nttgnyj."

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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.