Search for Clinical Trial Results
Iron Metabolism Disorders - 22 Studies Found
Status | Study |
Completed |
Study Name: Effects of Intravenous Injection of Erythropoietin on Hepcidin Pharmacokinetics in Healthy Volunteers Condition: Iron Metabolism Disorders Date: 2008-05-27 Interventions:
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Completed |
Study Name: Low Dose β-carotene Supplementation Diminishes Oxidative Stress in Type 2 Diabetics and Healthy Individuals Condition:
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Recruiting |
Study Name: Dose-escalation Trial of the Safety, Pharmacokinetics, and Pharmacodynamics of Iron Isomaltoside (Monofer®) Condition:
Interventions: Drug: Iron Isomaltoside The trial is a dose escalating trial. |
Recruiting |
Study Name: Extended Evaluation of Deferasirox Film-coated Tablet (FCT) Formulation Condition: Chronic Iron Overload Date: 2016-03-21 Interventions: Drug: Deferasirox Deferasirox FCT will be provided as 90 mg, 180 mg and 360 mg film-coated tablets for o |
Completed |
Study Name: Non-invasive Quantification of Liver Iron With MRI Condition:
Date: 2011-08-17 Interventions: Device: Non-contrast MRI Non-contrast MRI will be performed on each subject, at both 1.5T and 3.0T. Diff |
Completed |
Study Name: Retrospective Evaluation of Adult and Pediatric Transfusion-dependent Patients Treated With Deferasirox Therapy Condition: Iron Overload Date: 2013-05-26 |
Completed |
Study Name: Active Drug Surveillance Program of Ferriprox Use Condition: Transfusional Iron Overload Date: 2013-04-15 |
Terminated |
Study Name: Study for Transfusionally Iron Overloaded Children, Adolescents and Adults Using FBS0701 (SSP-004184) Condition: Iron Overload Due to Repeated Red Blood Cell Transfusions Date: 2012-08-16 Interventions: Drug: SSP-004184AQ Long term extension study of 8-75 mg/kg/d of SSP-004184AQ (equivalent to 7-68 mg/kg/d |
Terminated |
Study Name: Pharmacokinetics of SSP-004184 in the Treatment of Chronic Iron Overload Requiring Chelation Therapy Condition: Iron Overload Due to Repeated Red Blood Cell Transfusions Date: 2012-05-22 Interventions: Drug: SPD602 50 mg/kg/day orally twice daily for 24 weeks |
Recruiting |
Study Name: Massive Iron Deposit Assessment Condition:
Date: 2012-04-03 Interventions:
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