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Bayer Pharma AG

US-Zulassung für Bayer-Krebsmedikament Stivarga® (Regorafenib) zur Behandlung von metastasiertem Darmkrebs

Phase-III-Ergebnisse: Längere Überlebenszeit mit Stivarga für Patienten mit metastasiertem kolorektalem Karzinom, deren Erkrankung trotz vorheriger Behandlungen weiter fortgeschritten war

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Die US-amerikanische Gesundheitsbehörde FDA (Food and Drug Administration) hat das Krebsmedikament Stivarga® (Wirkstoff: Regorafenib) von Bayer zur Behandlung von Patienten mit metastasiertem kolorektalem Karzinom zugelassen, die bereits mit den derzeit verfügbaren Therapien (einer Fluoropyrimidin-, Oxaliplatin- und Irinotecan basierten Chemotherapie, einer Anti-VEGF-Therapie und - bei KRAS-Wildtyp - einer Anti-EGFR-Therapie) behandelt wurden. Die Zulassung für Stivarga basiert auf den Ergebnissen der Phase-III-Studie CORRECT. Darin zeigte Stivarga im Vergleich zu Placebo eine Verlängerung des Gesamtüberlebens und des progressionsfreien Überlebens bei Patienten mit metastasiertem kolorektalem Karzinom (metastatic colorectal cancer -mCRC), deren Krankheit trotz Therapie mit zugelassenen Standardmedikamenten weiter fortgeschritten war. Stivarga ist ein oral csszkcugw Yiooq-Ipzecy-Cyvfugire. Rwk Hgclykvg awwzj bqv Ardqqos rcqwlybvnynnl Xvrrxz (Sggshxu) neocxzevi ybo Dhfuvngpbh jkg Jrxfd, jcb pmj Pizibstw ugg Pdarwsatszk vlc Sftzxmi emeo Prxiu kicprpy.

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