drugset / Trial / NCT00171821

A Study Assessing the Efficacy and Safety of Deferasirox in Patients With Transfusion-dependent Iron Overload

NCT00171821 ↗

Phase 3 Completed 1784 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study uses a single arm, multi-center, open-label trial design. The study will assess the efficacy and safety of 52 weeks of treatment with deferasirox (ICL670) in patients with evidence of transfusion induced iron overload.

Timeline

Start
2005-04
Primary completion
2009-05
Completion
2010-07

Outcome

Met primary endpoint

paper Overall, there was a significant reduction in serum ferritin from baseline (-264 ng/mL; P<0.0001) PMID 19951979 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Deferasirox Unknown 20 mg/kg Oral