The overall aim of this study is to assess the efficacy and safety of AS1411, over a range of doses, when combined with cytarabine, in the treatment of patients with primary refractory or relapsed acute myeloid leukemia (AML).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
70
AS1411 IV administration continuously over 7 days. Dose either 10mg/kg/day or 40 mg/kg/day.
UCLA Medical Center
Los Angeles, California, United States
Univeristy of Colorado Health Cancer Center
Aurora, Colorado, United States
St. Francis Hospital and Health Center
Beech Grove, Indiana, United States
The prorportion of patients achieving a completel response (CR) after the first cycle of treatment in each treatment group
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University of Louisville, James Graham Brown Cancer Center
Louisville, Kentucky, United States
Washington University
St Louis, Missouri, United States
University of Nebraska Medical Center
Omaha, Nebraska, United States
Duke University Medical Center
Durham, North Carolina, United States
Medical University of South Carolina
Charleston, South Carolina, United States
Cancer Therapy and Research Center - Institute for Drug development
San Antonio, Texas, United States
Christchurch Hospital
Christchurch, New Zealand