19
Participants
Start Date
January 31, 2008
Primary Completion Date
December 31, 2009
Study Completion Date
December 31, 2009
ertumaxomab
Ertumaxomab will be intravenously administered to see if it can increase the patient's objective response rate.
Minneapolis
Lebanon
New York
Ottawa
Montreal
Lead Sponsor
Collaborators (1)
Fresenius Biotech North America
INDUSTRY
Neovii Biotech
INDUSTRY