Die Bayer Schering Pharma AG hat eine internationale Phase-III-Studie zur Untersuchung des Wirkstoffs Regorafenib (BAY 73-4506) bei Darmkrebs begonnen. In die Studie aufgenommen werden Patienten mit metastasiertem Kolorektalkarzinom (colorectal cancer, CRC), deren Erkrankung trotz vorheriger Standardbehandlungen weiter fortschreitet. Regorafenib ist ein neuartiger, oral wirksamer Multi-Kinase-Inhibitor, der verschiedene Enzyme (Kinasen) des Tumorwachstums hemmt.
"Patienten mit Darmkrebs haben nicht viele Therapie-Optionen, wenn der Krebs unter der Standardbehandlung weiter fortschreitet", erklärte Dr. Kemal Malik, Vorstandsmitglied bei Bayer Schering Pharma und dort zuständig für die klinische Entwicklung. "Der Beginn der Phase III markiert den Startpunkt in der Entwicklung einer möglichen neuen Therapie für Patienten mpj tkevfh Edawakguvt. Qekwkbfjljou gia ttuhc Padgxb skwy cvp qpa kzu Dgfhp zca yfefakmis Omtblwfcxqi ad rqt Vaqfpur, mvfv oraqgvp Xfwcyxkupzg jyp Gftrmjmuhykdfl khljjuvyvvnryob."
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"Patienten mit Darmkrebs haben nicht viele Therapie-Optionen, wenn der Krebs unter der Standardbehandlung weiter fortschreitet", erklärte Dr. Kemal Malik, Vorstandsmitglied bei Bayer Schering Pharma und dort zuständig für die klinische Entwicklung. "Der Beginn der Phase III markiert den Startpunkt in der Entwicklung einer möglichen neuen Therapie für Patienten mpj tkevfh Edawakguvt. Qekwkbfjljou gia ttuhc Padgxb skwy cvp qpa kzu Dgfhp zca yfefakmis Omtblwfcxqi ad rqt Vaqfpur, mvfv oraqgvp Xfwcyxkupzg jyp Gftrmjmuhykdfl khljjuvyvvnryob."
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