drugset / Trial / NCT00882076

Clofarabine, Etoposide, and Mitoxantrone for Relapsed and Refractory Acute Leukemias

NCT00882076

Phase 1 Terminated 22 enrolled Milton S. Hershey Medical Center
Non-randomizedFactorialOpen-labelTreatment

Summary

The purpose of this study is to establish toxicity and a maximum tolerated dose recommended phase 2 dose of Clofarabine in combination with Etoposide and Mitoxantrone for therapy of relapsed or refractory acute leukemias. The investigators will observe responses with these therapy agents and assess the impact of Clofarabine interacting with Etoposide in induction of DNA strand breaks.

Timeline

Start
2009-03
Primary completion
2011-03
Completion
2011-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Clofarabine Other / unclassified 10 mg/m2 Intravenous
Subject Clofarabine Other / unclassified 20 mg/m2 Intravenous
Subject Clofarabine Other / unclassified 25 mg/m2 Intravenous
Subject Clofarabine Other / unclassified 30 mg/m2 Intravenous
Subject Etoposide Small molecule 100 mg/m2
Subject Mitoxantrone Small molecule 8 mg/m2

Indications