53
Participants
Start Date
July 31, 2010
Primary Completion Date
November 30, 2012
Study Completion Date
November 30, 2012
BIBW 2992 low dose
patient receives low dose BIBW 2992 po daily on day 1 of 21 day cycle
BIBW 2992 high dose
patient receives high dose BIBW 2992 po daily on day 1 of 21 day cycle
pemetrexed
given intravenously on day 1 of a 21 day cycle
pemetrexed
given intravenously on day 1 of a 21 day cycle
BIBW 2992 high dose 6 day
patient receives high dose BIBW 2992 po daily on days 1-6 on 1 of 21 day cycle
pemetrexed
given intravenously on day 1 of a 21 day cycle
pemetrexed
given intravenously on day 1 of a 21 day cycle
pemetrexed
given intravenously on day 1 of a 21 day cycle
pemetrexed
given intravenously on day 1 of a 21 day cycle
BIBW 2992 low dose 6 day
patient receives low dose BIBW 2992 po daily on days 1-6 on day 1 of 21 day cycle
BIBW 2992 medium dose 6 day
patient receives medium dose BIBW 2992 po daily on day1 to 6 of a 21 day cycle
BIBW 2992 medium dose
patient receives medium dose BIBW 2992 po daily on day 1 of 21 day cycle
1200.92.1001 Boehringer Ingelheim Investigational Site, Edmonton
1200.92.1002 Boehringer Ingelheim Investigational Site, Hamilton
Lead Sponsor
Boehringer Ingelheim
INDUSTRY