Transfusional Iron Overload Clinical Trial
Official title:
Phase I Study to Examine the Effect of Deferasirox on Renal Hemodynamics in β-thalassemia Patients With Transfusional Iron Overload
The primary purpose of this study is to evaluate the effect of deferasirox on renal hemodynamics by determining glomerular filtration rate (GFR), renal plasma flow (RPF) and filtration fraction (FF).
n/a
Status | Clinical Trial | Phase | |
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Completed |
NCT00390858 -
A 4-year Extension Study to Core 1-year Study of Iron Chelation Therapy With Deferasirox in β-thalassemia Major Pediatric Patients With Transfusional Iron Overload.
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Phase 2 | |
Completed |
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Safety and Pharmacokinetic Study of Escalating Multiple Doses of an Iron Chelator in Patients With Iron Overload
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Phase 1 | |
Completed |
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Magnetic Resonance Imaging (MRI) Assessments of the Heart and Liver Iron Load in Patients With Transfusion Induced Iron Overload
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Phase 4 | |
Completed |
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Phase 2 | |
Withdrawn |
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Phase 2 | |
Completed |
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High-Tc Susceptometer to Monitor Transfusional Iron Overload
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Phase 2 | |
Completed |
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Active Drug Surveillance Program of Ferriprox Use
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N/A | |
Completed |
NCT01044186 -
A Protocol to Allow Treatment With ICL670 for Patients With or at Risk of Life-threatening Complications of Transfusional Iron Overload Who Are Unable to Tolerate Other Iron Chelators Because of Documented Severe Toxicity
|
Phase 2 | |
Completed |
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Extension Study of Iron Chelation Therapy With Deferasirox in Patients With Transfusional Iron Overload
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Phase 2 | |
Terminated |
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Myelodysplastic Syndrome (MDS) Gastrointestinal (GI) Tolerability Study
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Phase 4 | |
Completed |
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Safety and Pharmacodynamic Study of an Oral Iron Chelator Given for 6 Months to Patients With Iron Overload
|
Phase 2 | |
Terminated |
NCT01363908 -
Safety, Efficacy and Pharmacokinetics of an Oral Iron Chelator Given for a Year to Pediatric Patients With Iron Overload
|
Phase 2 |