Transfusional Iron Overload Clinical Trial
Official title:
Active Drug Surveillance Program of Ferriprox Use
Observational, open label, prospective, multi-center, post-marketing drug surveillance program.
A post-marketing, drug surveillance program evaluating the use, monitoring, benefits and adverse effects of Ferriprox under clinical conditions in newly treated patients. ;
Observational Model: Cohort, Time Perspective: Prospective
Status | Clinical Trial | Phase | |
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Completed |
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Phase 1 | |
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Phase 2 | |
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Phase 4 | |
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Phase 2 | |
Withdrawn |
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Phase 2 | |
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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
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Phase 2 | |
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Phase 2 | |
Terminated |
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Phase 4 | |
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Phase 2 | |
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Phase 2 |