Clinical Trials Directory

Trials / Completed

CompletedNCT00839982

Clofarabine and Cytarabine in Treating Older Patients With AML or High-Risk MDS

Study of Oral Clofarabine Plus Low-dose Cytarabine in Previously Treated AML and High-Risk MDS Patients at Least 60 Years of Age

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Fred Hutchinson Cancer Center · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Not accepted

Summary

This phase I/II trial studied the side effects and best dose of clofarabine when given together with cytarabine and to see how well they work in treating older patients with acute myeloid leukemia (AML) or high-risk myelodysplastic syndromes (MDS) that have relapsed or not responded to treatment.

Detailed description

PRIMARY OBJECTIVES: I. To estimate the maximum tolerated dose (MTD) of oral clofarabine when given with LDAC (cytarabine) in patients age \>= 60 with previously treated AML or high risk MDS. SECONDARY OBJECTIVES: I. To determine the response rate, disease-free survival (DFS), and overall survival (OS) after therapy with oral clofarabine and LDAC for previously treated AML or high-risk MDS. OUTLINE: This is a phase I, dose-escalation study of clofarabine followed by a phase II study. Patients receive clofarabine orally (PO) once daily (QD) on days 1-5 and low-dose cytarabine subcutaneously (SC) twice daily (BID) on days 1-10 or SC QD on days 1-14. Treatment repeats every 21-28 days for up to 4 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 3 months for 2 years and then annually for 3 years.

Conditions

Interventions

TypeNameDescription
DRUGclofarabineGiven PO
DRUGcytarabineGiven SC

Timeline

Start date
2008-11-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2009-02-10
Last updated
2017-07-11
Results posted
2017-07-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00839982. Inclusion in this directory is not an endorsement.