17
Participants
Start Date
October 1, 2010
Primary Completion Date
May 1, 2013
Study Completion Date
May 1, 2013
afatinib 20mg
patient to receive afatinib low dose po daily in combination with vinorelbine iv
afatinib 40mg
patient to receive afatinib high dose po daily in combination with vinorelbine iv
vinorelbine IV 25 or 20mg/m2
patient to receive standard dose vinorelbine once a week for four times per cycle
1200.84.003 Boehringer Ingelheim Investigational Site, Chuo-ku, Osaka, Osaka
1200.84.004 Boehringer Ingelheim Investigational Site, Kashiwa, Chiba
1200.84.001 Boehringer Ingelheim Investigational Site, Nagoya, Aichi
1200.84.002 Boehringer Ingelheim Investigational Site, Sakyo-ku, Kyoto, Kyoto
Lead Sponsor
Boehringer Ingelheim
INDUSTRY