95
Participants
Start Date
December 31, 2005
Primary Completion Date
June 30, 2008
Study Completion Date
July 31, 2008
Sorafenib (Nexavar, BAY43-9006)
Sorafenib 200 mg tablets (400 mg \[2 x 200 mg tablets\] twice daily \[bid\] or 400 mg once daily \[od\] or 400 mg every other day \[qod\]) administered orally
Akita
Asahi
Chiba
Chiba
Matsuyama
Fukuoka
Fukuoka
Kurume
Isesaki
Maebashi
Sapporo
Sapporo
Sapporo
Sunagawa
Tsukuba
Morioka
Kagoshima
Kyoto
Kyoto
Tsu
Natori-shi
Kashihara
Kurashiki
Okayama
Osaka
Sayama
Suita
Hidaka
Irima-gun
Tokorozawa
Hamamatsu
Sunto
Utsunomiya
Tokushima
Arakawa-ku
Bunkyo-ku
Chuo-ku
Itabashi-ku
Shinjuku-ku
Yamagata
Ube
Lead Sponsor
Bayer
INDUSTRY