Darbepoetin alfa once monthly corrects anaemia in patients with chronic kidney disease not on dialysis

Nephrology (Carlton). 2014 May;19(5):266-74. doi: 10.1111/nep.12214.

Abstract

Aim: While darbepoetin alfa (DA) can be administered once monthly (QM) to maintain haemoglobin (Hb) concentrations in anaemic patients with chronic kidney disease not on dialysis (CKD-ND), the QM use of DA for anaemia correction has not been previously investigated.

Methods: In this randomized, double-blind, non-inferiority, active-controlled study, adult subjects with CKD-ND, Hb levels <10 g/dL, and not treated with an erythropoiesis-stimulating agent were randomized 1:1 to receive DA every 2 weeks (Q2W) or QM for 33 weeks with initial doses of 0.75 μg/kg Q2W or 1.5 μg/kg QM. Subjects were treated to target Hb levels of 10-12 g/dL and ≥1 g/dL increase from baseline. The primary end-point was Hb change between baseline and the evaluation period (weeks 29-33), with a non-inferiority margin of -0.5 g/dL.

Results: Three hundred and fifty-five subjects received ≥1 dose of DA. Mean (95% confidence interval [CI]) change in Hb between baseline and the evaluation period was 2.16 (1.98-2.33) g/dL for the Q2W group and 1.97 (1.80-2.14) g/dL for the QM group, the mean (95% CI) difference in Hb change being -0.19 (-0.43 to 0.05) g/dL. Most subjects (97.9% Q2W; 98.1% QM) achieved a Hb level ≥10.0 g/dL and ≥1.0 g/dL increase in Hb from baseline. Mean DA (SD) weekly equivalent doses over the evaluation period were 0.20 (0.23) and 0.27 (0.31) μg/kg per week for the Q2W and QM groups, respectively. Safety profiles were similar between groups.

Conclusion: In subjects with CKD-ND, QM dosing was non-inferior to Q2W dosing for anaemia correction and had a similar safety profile.

Trial registration: ClinicalTrials.gov NCT00925587.

Keywords: anaemia; chronic kidney failure; darbepoetin alfa; haemoglobin; randomized controlled trial.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Anemia / blood
  • Anemia / diagnosis
  • Anemia / drug therapy*
  • Anemia / etiology
  • Australia
  • Biomarkers / blood
  • Darbepoetin alfa
  • Double-Blind Method
  • Drug Administration Schedule
  • Erythropoietin / administration & dosage
  • Erythropoietin / adverse effects
  • Erythropoietin / analogs & derivatives*
  • Europe
  • Female
  • Hematinics / administration & dosage*
  • Hematinics / adverse effects
  • Hemoglobins / metabolism
  • Humans
  • Male
  • Mexico
  • Middle Aged
  • Renal Insufficiency, Chronic / complications*
  • Renal Insufficiency, Chronic / diagnosis
  • Time Factors
  • Treatment Outcome
  • Up-Regulation
  • Young Adult

Substances

  • Biomarkers
  • Hematinics
  • Hemoglobins
  • Erythropoietin
  • Darbepoetin alfa

Associated data

  • ClinicalTrials.gov/NCT00925587