64
Participants
Start Date
July 3, 2012
Primary Completion Date
October 30, 2018
Study Completion Date
October 30, 2018
BT062 , intravenous administration
Dose escalation to determine dose limiting toxicities (DLTs) and/or the maximum tolerated dose (MTD)/recommended Phase II dose (RPTD) of BT062 in combination with lenalidomide/dexamethasone
Mount Sinai Medical Center, New York
Emory University Winship Cancer Institute, Atlanta
Mayo Clinic, Jacksonville
Memorial Healthcare System, Pembroke Pines
The University of Chicago, Chicago
University of Texas Health Science Center, San Antonio
USC Norris Comprehensive Cancer Center, Los Angeles
City of Hope, Duarte
Dana-Farber Cancer Institute, Boston
Hackensack University Medical Center, Hackensack
Lead Sponsor
Collaborators (1)
Biotest
INDUSTRY
Biotest Pharmaceuticals Corporation
INDUSTRY