drugset / Trial / NCT00641589

A Study to Determine the Pharmacokinetic and Pharmacodynamic Profiles of PROCRIT (Epoetin Alfa) in Anemic Patients With Chronic Kidney Disease

NCT00641589

RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to describe how four different dosing regimens of PROCRIT (epoetin alfa) are utilized in patients with anemia due to non-dialysis chronic kidney disease (CKD).

Timeline

Start
2006-01
Primary completion
Completion
2006-11

Drugs

EvaluationDrugModalityDoseRoute
Subject epoetin alfa Protein / enzyme biologic 50 iu/kg
Subject epoetin alfa Protein / enzyme biologic 10000 iu
Subject epoetin alfa Protein / enzyme biologic 20000 iu
Subject epoetin alfa Protein / enzyme biologic 40000 iu