drugset / Trial / NCT00048035

A Study of Intravenous (iv) Mircera in Hemodialysis Patients With Chronic Renal Anemia

NCT00048035

Phase 2 Completed 91 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will determine the appropriate dose and frequency of administration of iv Mircera maintenance therapy in hemodialysis patients with chronic renal anemia who were previously receiving iv epoetin. The anticipated time on study treatment is 3-12 months and the target sample size is \<100 individuals.

Timeline

Start
2002-03
Primary completion
2005-06
Completion
2005-06

Drugs

EvaluationDrugModalityDoseRoute
Subject methoxy polyethylene glycol-epoetin beta Protein / enzyme biologic 0.25 ug/kg Intravenous
Subject methoxy polyethylene glycol-epoetin beta Protein / enzyme biologic 0.4 ug/kg Intravenous
Subject methoxy polyethylene glycol-epoetin beta Protein / enzyme biologic 0.6 ug/kg Intravenous

Indications