drugset / Trial / NCT00481143

Efficacy and Safety of Deferasirox in Patients With Myelodysplastic Syndrome and Transfusion-dependent Iron Overload

NCT00481143

Phase 4 Completed 63 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to investigate the effects of iron chelation using deferasirox in low and INT-1 risk (referring to the international prognostic scoring system, IPSS) MDS patients who show signs of iron overload due to repeated blood transfusions. This trial is not recruiting patients in the United States.

Timeline

Start
2007-05
Primary completion
2010-11
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Deferasirox Unknown 6 mg/kg Oral
Subject Deferasirox Unknown 20 mg/kg Oral
Subject Deferasirox Unknown 30 mg/kg Oral