The primary objective is to determine the response rate (CR + PR) with CAMPATH-1H in patients with b-cell chronic lymphocyte leukemia (CLL) who have received an alkylating agent and who have failed fludarabine therapy. Secondary objectives are 1) to evaluate the safety profile of CAMPATH-1H in this population; and 2) to evaluate the clinical benefit of CAMPATH-1H in this population.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000865-26S1
Application #
6265335
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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