drugset / Trial / NCT01023035

Boceprevir/Peginterferon/Ribavirin for Chronic Hepatitis C: Erythropoietin Use Versus Ribavirin Dose Reduction for Anemia (P06086 AM2)

NCT01023035

Phase 3 Completed 687 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The current trial is designed to prospectively explore the safety of erythropoietin use for the treatment of anemia during boceprevir plus peginterferon alfa-2b/Ribavirin (PEG2b/RBV) therapy and to assess its relationship to efficacy. All participants in this trial will be treated with the triple combination of boceprevir plus PEG2b/RBV. If a participant becomes anemic during treatment, the participant will be randomized to one of two therapeutic strategies for management of anemia (erythropoietin use versus RBV dose reduction).

Timeline

Start
2009-12-07
Primary completion
2011-10-26
Completion
2011-10-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 600 mg Oral
Subject Ribavirin Small molecule 1400 mg Oral
Subject epoetin alfa Protein / enzyme biologic 40000 iu Subcutaneous
Background Boceprevir Small molecule 800 mg Oral
Background Peginterferon alfa-2b Protein / enzyme biologic 1.5 ug/kg Subcutaneous