drugset / Trial / NCT00117507

Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients

NCT00117507

Phase 4 Completed 24 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

Thirty patients were to be enrolled and 24 patients were actually enrolled into this open-label, single-arm trial designed to assess the safety and tolerability of oral deferasirox in adult transfusion dependent myelodysplastic syndrome (MDS) patients with iron overload. Patients enrolled in this study had low or intermediate (INT-1) risk MDS per International Prognostic Scoring System (IPSS) criteria. All patients initiated treatment with 20mg/kg/day deferasirox. Deferasirox were administered orally once per day for 12 months.

Timeline

Start
2005-09
Primary completion
2008-01
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Deferasirox Unknown 20 mg/kg Oral