drugset / Trial / NCT02640157

A Study Comparing Efficacy and Safety of ABT-493/ABT-530 to Sofosbuvir Dosed With Daclatasvir in Adults With HCV Genotype 3 Infection

NCT02640157 ↗

Phase 3 Completed 506 enrolled AbbVie
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to compare the safety and efficacy of ABT-493/ABT-530 to the combination of sofosbuvir (SOF) and daclatasvir (DCV) in adults with genotype 3 (GT3) chronic hepatitis C virus (HCV) infection.

Timeline

Start
2015-12
Primary completion
2016-10
Completion
2017-02

Outcome

Met primary endpoint

registry analysis (non-inferiority test); Arm A vs Arm B; Difference in percentage of participants -1.2 (95% CI -5.6 to 3.1) NCT02640157 ↗

registry analysis (non-inferiority test); Arm A; percentage of participants 95.3 (97.5% CI 92.2 to 98.4) NCT02640157 ↗

release “ENDURANCE-3 study, 95 percent (n=149/157) of GT3 chronic HCV-infected patients without cirrhosis and who were new to treatment achieved sustained virologic response” enanta.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Daclatasvir Small molecule 60 mg —
Comparator Sofosbuvir Small molecule 400 mg —
Subject glecaprevir Other / unclassified 300 mg —
Subject pibrentasvir Other / unclassified 120 mg —