drugset / Trial / NCT00239616

Pharmacokinetic of Intravenous Iron Sucrose in Adolescents on Hemodialysis or Peritoneal Dialysis Receiving Epoetin

NCT00239616

Phase 2 Completed 10 enrolled American Regent, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter pharmacokinetic study of Hemodialysis (HD) or Peritoneal Dialysis (PD) patients receiving erythropoietin. Patients were administered 100mg of iron sucrose undiluted by slow IV push over 5 minutes. Patients underwent serial blood draws and were subsequently followed for 7 days for safety endpoints.

Timeline

Start
2002-06-05
Primary completion
2003-09-15
Completion
2003-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron sucrose Unknown 100 mg Intravenous

Indications