54
Participants
Start Date
October 31, 2009
Primary Completion Date
December 31, 2012
Study Completion Date
December 31, 2012
BMS-754807
Tablets, Oral, doses vary during dose escalation, once daily, varies - treatment is continued to disease progression or MD/subject/sponsor decision
cetuximab (Erbitux®)
IV infusion, IV, 400 mg/m² loading dose, then 250 mg/m², weekly, varies - treatment is continued to disease progression or MD/subject/sponsor decision
Duke University Medical Center, Durham
University Of Wisconsin, Madison
Nebraska Methodist Hospital, Omaha
Local Institution, Vancouver
Local Institution, Toronto
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY