The primary objectives of this study are to evaluate the safety and tolerability and determine the maximally tolerated dose of humanized monoclonal antibody Hu1D10 administered to patients with previously treated non-Hodgkin's lymphoma expressing the antigen recognized by 1D10 and to measure pharmacokinetics to compare pharmacology at different dose levels and determine the optimal biological dose of Hu1D10.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000059-40
Application #
6422342
Study Section
Special Emphasis Panel (ZRR1)
Project Start
2000-12-01
Project End
2001-11-30
Budget Start
Budget End
Support Year
40
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
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