131
Participants
Start Date
November 30, 2004
Primary Completion Date
March 31, 2006
Study Completion Date
March 31, 2006
Nexavar (Sorafenib, BAY43-9006)
BAY 43-9006 400mg b.i.d. Treatment will continue until progression of underlying disease, unacceptable toxicity whose causal relationship to the study drug cannot be ruled out and which requires discontinuation of the drug, or consent withdrawal.
Nagoya
Akita
Asahi
Chiba
Chiba
Matsuyama
Fukuoka
Fukuoka
Kurume
Isesaski
Maebashi
Sapporo
Sapporo
Sapporo
Sapporo
Sunagawa
Tsukuba
Morioka
Kita
Kagoshima
Kyoto
Kyoto
Tsu
Natori-shi
Sendai
Nagasaki
Kashihara
Niigata
Kurashiki
Okayama
Osaka
Sayama
Suita
Irima-gun
Tokorozawa
Hamamatsu
Sunto
Utsunomiya
Tokushima
Wakayama
Wakayama
Yamagata
Ube
Nakakoma
Tokyo
Tokyo
Tokyo
Tokyo
Tokyo
Tokyo
Tokyo
Lead Sponsor
Bayer
INDUSTRY