The purpose of this study is to provide an opportunity for patients who exhibit progressive disease while receiving placebo on the companion 93-04-11 study to receive ONTAK. It is also designed to determine the effectiveness of ONTAK in Cutaneous T-cell Lymphoma (CTCL) patients whose tumors do not express CD25.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
86
Objective Rate of Response (ORR), defined as CR + CCR + PR
Time-to-Treatment Failure
Time-to-Progression
Duration of Response
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University of Texas, M.D. Anderson Cancer Center
Houston, Texas, United States
Level 4 Department of Haematology Royal North Shore Hospital
Saint Leonard's, New South Wales, Australia
Westmead Hospital, Department of Haematology
Westmead, New South Wales, Australia
Mater Misericordiae Adult Hospital
South Brisbane, Queensland, Australia
Oncology Haematology Radiation Oncology Unit, Princess Alexandra Hospital
Woolloongabba, Queensland, Australia
Peter MacCallum Cancer Institute
Melbourne, Victoria, Australia
LKH Universitatsklinikum Graz
Graz, Austria
Allgemeines Krankenhaus der Stadt Wien
Vienna, Austria
Cross Cancer Centre
Edmonton, Alberta, Canada
Hamilton Regional Cancer Center
Hamilton, Ontario, Canada
...and 24 more locations