drugset / Trial / NCT01652872

Strategies Using Darbepoetin Alfa to Avoid Transfusions in Chronic Kidney Disease

NCT01652872

Phase 3 Completed 756 enrolled Amgen
RandomizedParallel-groupTriple-blindTreatment

Summary

A phase 3, multicenter, randomized, double-blind, parallel group study. Anemic subjects with chronic kidney disease (CKD) and not on dialysis will be randomized 1:1 to 1 of 2 dosing strategies to evaluate the proportion of subjects receiving at least one red blood cell (RBC) transfusion. In the haemoglobin (Hb)-based titration group, darbepoetin alfa doses will be titrated to maintain Hb ≥ 10.0 grams/deciliter (g/dL). In the fixed dose group, subjects will receive a fixed dose of darbepoetin alfa. Treatment group, darbepoetin alfa doses, and protocol specified Hb concentrations will be blinded. Subjects will be followed for approximately 2 years from the date of randomization.

Timeline

Start
2012-07-30
Primary completion
2017-10-19
Completion
2017-10-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Darbepoetin alfa Protein / enzyme biologic 0.45 ug/kg Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 10 ug Subcutaneous
Subject Darbepoetin alfa Protein / enzyme biologic 300 ug Subcutaneous

Indications

No indication recorded.