61
Participants
Start Date
August 31, 2009
Primary Completion Date
November 30, 2011
Study Completion Date
February 29, 2012
BI-6727
Low to high dose (administered every 3 weeks). Depending on the toxicities observed, intermediary dose levels may be added
BI 6727
low to high dose
1230.6.3201 Boehringer Ingelheim Investigational Site, Brussels
1230.6.3202 Boehringer Ingelheim Investigational Site, Leuven
Lead Sponsor
Boehringer Ingelheim
INDUSTRY