1
Participants
Start Date
December 31, 2009
Primary Completion Date
July 31, 2010
Study Completion Date
July 31, 2010
teplizumab
Cohorts 1-5: escalating doses of subcutaneously administered teplizumab; cohort 6: intravenous administration of maximum tolerated subcutaneous dose.
University of Michigan Medical Center, Ann Arbor
Oregon Health & Science University, Portland
Lead Sponsor
Eli Lilly and Company
INDUSTRY
MacroGenics
INDUSTRY