drugset / Trial / NCT02113631

Comparative Effectiveness and Tolerability of Boceprevir vs Telaprevir

NCT02113631

Completed 50 enrolled Louis Stokes VA Medical Center
RandomizedParallel-groupOpen-labelTreatment

Summary

1. The primary objective is to study the comparative effectiveness and tolerability of boceprevir vs. telaprevir in HCV treatment, within the VA population. 2. The secondary objective: * Resource use: recording of differences in resource use, such as direct costs (e.g., drug acquisition costs) and other indirect cost (e.g., staff utilization etc.) as the study will not only derive data by comparing those two drugs but also study the effect on different treatment lengths.

Timeline

Start
2011-09
Primary completion
2013-04
Completion
2013-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Boceprevir Small molecule 800 mg Oral
Comparator Telaprevir Small molecule 1125 mg Oral
Comparator Peginterferon alfa-2a Protein / enzyme biologic 45 ug Subcutaneous
Comparator Peginterferon alfa-2a Protein / enzyme biologic 180 ug Subcutaneous
Comparator Ribavirin Small molecule 800 mg
Comparator Ribavirin Small molecule 1200 mg