drugset / Trial / NCT00875745

Combination of Sorafenib and Vorinostat in Poor-risk Acute Myelogenous Leukemia (AML) and High Risk Myelodysplastic Syndrome (MDS)

NCT00875745

Phase 1 Completed 15 enrolled Indiana University Bayer · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to test the safety of sorafenib and vorinostat when given together to see what effects (good and bad) it has on the patient and their acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). This study is also being done to find the highest dose of sorafenib and vorinostat that can be given together without causing severe side effects.

Timeline

Start
2009-04
Primary completion
2010-05
Completion
2013-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Sorafenib Small molecule 400 mg Oral
Subject Vorinostat Small molecule 100 mg Oral