drugset / Trial / NCT01652872
Strategies Using Darbepoetin Alfa to Avoid Transfusions in Chronic Kidney Disease
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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.