drugset / Trial / NCT04111367

Study of Seraprevir in Combination With Sofosbuvir in Chronic Genotype 2,3,6 Hepatitis C Virus Infection Patients

NCT04111367

Phase 2 Unknown 36 enrolled Ginkgopharma CO., LTD
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study was to assess the safety and efficacy of Seraprevir in combination with sofosbuvir in patients with Hepatitis C (HCV) genotype2,3,6. Efficacy was assessed by the rate of sustained viral response (SVR) 12 weeks after the discontinuation of therapy (SVR12).

Timeline

Start
2019-04-03
Primary completion
2020-04-30
Completion
2020-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Seraprevir Unknown 100 mg Oral
Subject Sofosbuvir Small molecule 400 mg Oral