drugset / Trial / NCT02340962

Evaluate the Efficacy and Safety of TG-2349 in Subjects With Hepatitis C Infection

NCT02340962

Phase 2 Completed 25 enrolled TaiGen Biotechnology Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

A Phase 2, Multicenter, Randomized, Open-label, Dose-ranging Study to Evaluate the Efficacy and Safety of TG-2349 in Combination with Peg-interferon and Ribavirin in Treatment Naïve East Asian Subjects with Chronic Hepatitis C Virus Genotype 1b Infection.

Timeline

Start
2015-05
Primary completion
2016-08-12
Completion
2016-10-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Furaprevir Small molecule 200 mg Oral
Subject Furaprevir Small molecule 400 mg Oral
Background Ribavirin Small molecule Oral
Background interferon alfa Protein / enzyme biologic 180 ug Subcutaneous