drugset / Trial / NCT02233504

Pilot Study to Assess Hematologic Response in Patients With Acute Myeloid Leukemia or High Risk Myelodysplastic Syndromes Undergoing Monotherapy With Exjade (Deferasirox)

NCT02233504

Phase 0 Completed 25 enrolled Abramson Cancer Center at Penn Medicine
NaSingle-groupTreatment

Summary

The purpose of this trial is to examine the hematologic response rate of Exjade® in patients with AML and high risk MDS and chronic iron overload from blood transfusions. Deferasirox has been developed as an iron-chelating agent, and unlike deferoxamine, a previously developed iron chelator, deferasirox has the advantage of oral administration.

Timeline

Start
2014-08
Primary completion
2017-10
Completion
2017-10-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Deferasirox Unknown Oral