Acute Myeloid Leukemia Clinical Trial

Phase II Study of AS1411 Combined With Cytarabine to Treat Acute Myeloid Leukemia

Summary

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).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

primary refractory or relapsed AML
confirmed diagnosis of AML (de novo or secondary) as defined by WHO classification (Vardiman 2002)
aged at least 18 years

Exclusion Criteria:

initial diagnosis of acute promyelocytic leukemia as defined by French-American-British criteria (Bennett 1976)
patient in blast crisis stage of chronic myeloid leukemia
received high-dose cytarabine (total cumulative dose of >6g/m sq)in last 6 months
interval of <6 months between first onset of last complete remission and current relapse
those with primary refractory leukemia who have received more than three previous induction cycles
relapsed patients who have received more than three previous treatment regimens

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 2

Estimated Enrollment:

70

Study ID:

NCT00512083

Recruitment Status:

Completed

Sponsor:

Antisoma Research

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There are 9 Locations for this study

See Locations Near You

UCLA Medical Center
Los Angeles California, 90095, United States
Univeristy of Colorado Health Cancer Center
Aurora Colorado, 80010, United States
St. Francis Hospital and Health Center
Beech Grove Indiana, 46107, United States
University of Louisville, James Graham Brown Cancer Center
Louisville Kentucky, 40202, United States
Washington University
St Louis Missouri, 63110, United States
University of Nebraska Medical Center
Omaha Nebraska, 68198, United States
Duke University Medical Center
Durham North Carolina, 27710, United States
Medical University of South Carolina
Charleston South Carolina, 29425, United States
Cancer Therapy and Research Center - Institute for Drug development
San Antonio Texas, 78229, United States
Christchurch Hospital
Christchurch , , New Zealand

How clear is this clinincal trial information?

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 2

Estimated Enrollment:

70

Study ID:

NCT00512083

Recruitment Status:

Completed

Sponsor:


Antisoma Research

How clear is this clinincal trial information?

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