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Ferumoxytol Versus Oral Iron in the Treatment of Anemia in Hemodialysis Patients

Anemia Clinical Trial

Official title:
A Phase III Study of the Safety and Efficacy of Ferumoxytol (Compared With Oral Iron) as an Iron Replacement Therapy in Hemodialysis Patients Who Are Receiving Supplemental EPO Therapy

Clinical Trial Summary

The study will evaluate the safety and efficacy of a new intravenously administered iron drug to treat anemia in patients on hemodialysis.

Clinical Trial Description

This study will evaluate the efficacy and safety of intravenous (IV) iron (ferumoxytol) as compared to oral iron in the treatment of anemia in hemodialysis patients receiving erythropoietin. Patients are randomized to receive either two doses of 510 mg of intravenous ferumoxytol in sequential dialysis sessions or 200 mg oral elemental iron daily for three weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00233597
Study type Interventional
Source AMAG Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 3
Start date August 2004
Completion date March 2007
View Details
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