drugset / Trial / NCT00749515

Pilot Study for Patients With Poor Response to Deferasirox

NCT00749515

Phase 4 Completed 15 enrolled Boston Children's Hospital Novartis · collab
NaSingle-groupOpen-labelTreatment

Summary

This purpose of this study is to understand the differences between people who have a good response to deferasirox (exjade) compared to people who have a poor response to this medication when used for transfusion-dependent iron overload. The hypothesis is that patients with poor responses have physiologic barriers to deferasirox that may include absorption, pharmacokinetics of drug metabolism, hepatic clearance and/or genetic factors.

Timeline

Start
2008-03
Primary completion
2008-10
Completion
2008-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Deferasirox Unknown 35 mg/kg Oral
Subject Deferoxamine Other / unclassified 50 mg/kg