Bayer HealthCare und Onyx Pharmaceuticals haben eine weitere internationale Phase-III-Studie mit Nexavar® (Wirkstoff: Sorafenib) in der Indikation Lungenkrebs begonnen. In die Studie sollen Patienten mit fortgeschrittenem nicht-kleinzelligem Lungenkarzinom (Non-small cell lung cancer = NSCLC) aufgenommen werden, die bereits zwei oder drei vorherige Therapien erhalten hatten. Untersucht werden Patienten aller Histologien (Zellarten) außer denen mit Plattenepithelkarzinom.
"Nexavar hat seine Wirksamkeit bei zwei Tumortypen bewiesen. Unser Ziel ist es nun, den Einsatz von Nexavar bei einer Vielzahl anderer solider Tumoren zu untersuchen", so Dr. Dimitris Voliotis, zuständig für die klinische Entwicklung von Nexavar bei Bayer HealthCare. "Auf Basis der positiven Ergebnisse vorausgegangener Ccmhsbg uacfhxp krz bu rir Jiminihxg wbz Folvjgq xsj Tgjdhelypnhi nfp Aireslwom jgy ZNPFP."
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"Nexavar hat seine Wirksamkeit bei zwei Tumortypen bewiesen. Unser Ziel ist es nun, den Einsatz von Nexavar bei einer Vielzahl anderer solider Tumoren zu untersuchen", so Dr. Dimitris Voliotis, zuständig für die klinische Entwicklung von Nexavar bei Bayer HealthCare. "Auf Basis der positiven Ergebnisse vorausgegangener Ccmhsbg uacfhxp krz bu rir Jiminihxg wbz Folvjgq xsj Tgjdhelypnhi nfp Aireslwom jgy ZNPFP."
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