drugset / Trial / NCT00605293

A Study of Intravenous Mircera (C.E.R.A or Methoxy Polyethylene Glycol-epoetin Beta) for the Maintenance Treatment of Hemodialysis Participants With Chronic Renal Anemia

NCT00605293

Phase 3 Completed 101 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This 2 arm study will compare the efficacy and safety of monthly administration of intravenous (IV) Mircera versus epoetin alfa for the maintenance of hemoglobin levels in hemodialysis patients with chronic renal anemia. Participants currently receiving maintenance treatment with epoetin alfa will be randomized either to receive monthly injections of 120, 200 or 360 micrograms Mircera, with the starting dose derived from the dose of epoetin alfa they were receiving in the week preceding study start, or to continue on epoetin alfa treatment. The anticipated duration of study is 32 weeks, and the target sample size is 146 participants.

Timeline

Start
2008-01
Primary completion
2010-01
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator epoetin alfa Protein / enzyme biologic 7443 iu Intravenous
Subject methoxy polyethylene glycol-epoetin beta Protein / enzyme biologic 120 ug Intravenous
Subject methoxy polyethylene glycol-epoetin beta Protein / enzyme biologic 200 ug Intravenous
Subject methoxy polyethylene glycol-epoetin beta Protein / enzyme biologic 360 ug Intravenous

Indications