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NCT04001608

Study of Seraprevir in Combination With Sofosbuvir in Chronic Genotype 1 Hepatitis C Virus Infection Patients

Status unknown Phase 3 Last updated 28 June 2019
What this trial tests

Phase 3 trial testing Seraprevir in Hepatitis C Virus Infection in 206 participants. Status unknown.

Timeline
17 October 2018
Primary endpoint
31 July 2019
30 November 2019

Quick facts

Lead sponsorGinkgopharma CO., LTD
PhasePhase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment206
Start date17 October 2018
Primary completion31 July 2019
Estimated completion30 November 2019
Sites22 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Ginkgopharma CO., LTD — full company profile →

Who can join

Adults 18 to 75, any sex, with Hepatitis C Virus Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study was to assess the safety and efficacy of Seraprevir in combination with sofosbuvir administered for 12 weeks in patients with Hepatitis C (HCV) genotype1. Efficacy was assessed by the rate of sustained viral response (SVR) 12 weeks after the discontinuation of therapy (SVR12).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Antiviral Classification
    · 2021

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Other trials of Seraprevir

Trials testing the same drug.

Other recruiting trials for Hepatitis C Virus Infection

Currently open trials in the same condition.

Other Ginkgopharma CO., LTD trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04001608.

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