drugset / Trial / NCT00469560

Safety, Tolerability, and Efficacy of Deferasirox in MDS

NCT00469560

Phase 3 Completed 158 enrolled GIMEMA Foundation
NaSingle-groupOpen-labelTreatment

Summary

Open label, single arm study on Deferasirox treatment in MDS patients with chronic transfusional hemosiderosis. Patients receive daily oral dosis of Deferasirox in order to eliminate the quantity of iron administered during transfusions and, if needed, to reduce the overload of already present iron. After an screening phase in which patients are evaluated according to eligibility criteria, a one year treatment phase foresees monthly visits to evaluate safety and efficacy signs.

Timeline

Start
2007-06
Primary completion
2010-03
Completion
2013-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Deferasirox Unknown Oral