drugset / Trial / NCT01001143

Intravenous (IV) Decitabine and Oral Bexarotene for Acute Myelogenous Leukemia (AML)

NCT01001143

Phase 1 Completed 19 enrolled Washington University School of Medicine
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main objective is to determine the safety and tolerability of combination decitabine and bexarotene during four cycles of therapy.

Timeline

Start
2010-05
Primary completion
2013-05
Completion
2014-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Bexarotene Small molecule 100 mg/m2 Oral
Subject Bexarotene Small molecule 200 mg/m2 Oral
Subject Bexarotene Small molecule 300 mg/m2 Oral
Subject Decitabine Small molecule 20 mg/m2 Intravenous