drugset / Trial / NCT00121602

Efficacy Study: Darbepoetin Alfa for the Treatment of Anemia in Patients With Chronic Kidney Disease

NCT00121602

Phase 3 Completed 446 enrolled Amgen
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate whether the efficacy of darbepoetin alfa SF is equivalent to that of darbepoetin alfa RB for the treatment of anemia in patients with chronic kidney disease (CKD) receiving hemodialysis.

Timeline

Start
2005-03
Primary completion
2005-10
Completion
2006-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Darbepoetin alfa Protein / enzyme biologic 10 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 15 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 20 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 30 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 40 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 50 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 60 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 80 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 100 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 150 ug Subcutaneous