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Source:
Phase II Trial Evaluating Low-dose Deferasirox (DFX) in Patients With Low-risk (MDS) Myelodysplastic Syndrome Resistant or Relapsing After ESA Agents (LODEFI)
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Source:
A Phase II, Multicenter, Open-label, Randomized Two-year Study to Evaluate the Efficacy and Safety of Deferasirox Film-coated Tablet Versus Phlebotomy in Patients With
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Source:
A Randomized, Open-label, Multicenter, Two Arm, Phase II Study to Evaluate Treatment Compliance, Efficacy and Safety of an Improved Deferasirox Formulation (Granules) in
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Source:
Comparison of Deferasirox and Desferoxamine in Patients of β-Thalassemia Major With Iron Overload
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Deferasirox Versus Venesection in Patients With Hemochromatosis and for Treatment of Transfusional Siderosis in Myelodysplastic Syndrome: Diagnostics and New
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Authors :
Novartis; Ellis Neufeld, Professor of Pediatrics
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Source:
Pilot Pharmacokinetic Study In Patients With Inadequate Response To Deferasirox (Exjade)Chirnomas D, Smith AL, Braunstein J, Finkelstein Y, Pereira L, Bergmann AK,
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Source:
Identification of Risk Factors and Measures to Prevent Liver and Pancreas Complications in Pediatric Patients Undergoing a Hematopoietic Stem Cell Transplant (HSCT)Maximova N, Zanon D, Pascolo
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The Deferasirox-AmBisome Therapy for Mucormycosis (DEFEAT Mucor) StudySpellberg B, Edwards J Jr, Ibrahim A. Novel perspectives on mucormycosis: pathophysiology,
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Authors :
Erfan Nur, Principal Investigator
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Source:
Low Dose Iron Chelation as TReatment of Oxidative Damage in Patients With Sickle Cell Disease: the TROS Study
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Source:
Early and Low Dose Deferasirox (3.5 mg/kg FCT) to Suppress NTBI and LPI as Early Intervention to Prevent Tissue Iron Overload in Lower Risk MDS
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