drugset / Trial / NCT00548691

Safety and Tolerability of FCM vs Standard of Care in Treating Iron Deficiency Anemia in Chronic Kidney Disease Patients

NCT00548691

Phase 3 Completed 513 enrolled American Regent, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The Objective of this study is to study the safety of FCM in patients with anemia caused by chronic kidney failure

Timeline

Start
2007-10
Primary completion
2009-01
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Ferric carboxymaltose Other / unclassified 15 mg/kg Intravenous
Subject Ferric carboxymaltose Other / unclassified 200 mg Intravenous

Indications