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Study of Deferasirox Relative to Subcutaneous Deferoxamine in Sickle Cell Disease Patients

Sickle Cell Disease Clinical Trial

Official title:
A Randomized, Open-label, Multi-center, Phase II Study to Evaluate the Safety and Efficacy of Deferasirox (ICL670) 20 mg/kg/Day Relative to Subcutaneous Deferoxamine in Sickle Cell Disease Patients With Iron Overload From Repeated Blood Transfusions

Clinical Trial Summary

This study will examine the long-term safety and efficacy of Deferasirox in patients with sickle cell disease and iron overload from repeated blood transfusions.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00110617
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date May 2005
Completion date April 2008
View Details
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