28
Participants
Start Date
May 31, 2008
Primary Completion Date
March 31, 2012
Study Completion Date
March 31, 2012
Elotuzumab (HuLuc63)
Cohort 1 - 2.5 mg/kg elotuzumab IV with bortezomib on Days 1 \& 11, with only Bortezomib IV on Days 4 \& 8; Cohort 2 - 5.0 mg/kg elotuzumab IV with bortezomib on Days 1 \& 11, with only Bortezomib IV on Days 4 \& 8; Cohort 3 - 10.0 mg/kg elotuzumab IV withbortezomib on Days 1 \& 11, with only Bortezomib IV on Days 4 \& 8; and Cohort 4 - 20.0 mg/kg elotuzumab IV with bortezomib on Days 1 \& 11, with only Bortezomib IV on Days 4 \& 8.
Site Reference ID/Investigator# 63850, Buffalo
Site Reference ID/Investigator# 63849, Columbus
Site Reference ID/Investigator# 63855, Chicago
Site Reference ID/Investigator# 63853, Los Angeles
Site Reference ID/Investigator# 63848, Seattle
Site Reference ID/Investigator# 63847, Boston
Site Reference ID/Investigator# 63852, Ann Arbor
Site Reference ID/Investigator# 63854, Hackensack
Lead Sponsor
Collaborators (1)
Bristol-Myers Squibb
INDUSTRY
Abbott
INDUSTRY