drugset / Trial / NCT01590225

Efficacy and Safety of Boceprevir in Combination With Peginterferon Alfa-2b Plus Ribavirin in Pediatric Subjects With Chronic Hepatitis C Genotype 1 (P08034)

NCT01590225

Phase 3 Withdrawn Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a three-part (Part A, Part B, and Part C), open-label, multicenter study of boceprevir in pediatric participants with chronic hepatitis C (CHC) genotype 1 (GT1). In Part A and Part B, efficacy and safety will be evaluated in participants with CHC GT1 who are non-cirrhotic, treatment naïves (Part A) or who are non-cirrhotic, treatment failures to (peg)interferon/ribavirin or who are cirrhotics (whether treatment naïve or treatment failure) (Part B). Part C is long-term follow up and no study treatment will be administered during this period, but participants who do not achieve viral clearance will be allowed to receive other treatments for CHC.

Timeline

Start
2013-01-28
Primary completion
2021-08-18
Completion
2021-08-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Boceprevir Small molecule 11.4 mg/kg Oral
Subject Peginterferon alfa-2b Protein / enzyme biologic 60 ug/m2 Subcutaneous
Subject Ribavirin Small molecule 15 mg/kg Oral