Efficacy and Safety of Coblopasvir Hydrochloride Capsules Combined With Sofosbuvir Tablets for the Treatment of Chronic HCV Infection: A Prospective, Multi-center Real-world Study.

Sponsor
Beijing Tsinghua Chang Gung Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05601518
Collaborator
(none)
450
1
14
32.2

Study Details

Study Description

Brief Summary

Chronic hepatitis C is a long-lasting infectious disease caused by hepatitis C virus (HCV). According to statistics by the World Health Organization (WHO), the global HCV prevalence is estimated at 2.8%, equating to approximately 185 million. Chronic HCV infection can lead to chronic inflammatory necrosis and fibrosis in the liver, and in some patients can develop into hepatic cirrhosis and even hepatocellular carcinoma (HCC), endangering the health and life of patients.

The development of direct-acting antiviral agents (DAAs) since 2011 markedly improved antiviral efficacy and significantly shortened treatment cycle, making the drugs convenient for clinical use. Small molecule DAAs exert target-specific effects on proteins involved in the HCV life cycle and have been included in the treatment guidelines by leading associations for the study of liver diseases worldwide.

Treatment regimen for hepatitis C - coblopasvir hydrochloride capsules combined with sofosbuvir tablets:

Coblopasvir hydrochloride capsule is an NS5A inhibitor that inhibits the replication and assembly of HCV, and sofosbuvir tablet is a NS5B polymerase inhibitor. The primary efficacy results (sustained virologic response 12 weeks post-treatment, SVR12) were comparable between the phase II and III clinical studies: the overall SVR12 in subjects was 97%. The SVR12 after coblopasvir hydrochloride capsules combined with sofosbuvir tablets in genotype 3 infection with cirrhosis and genotype 3b infection with cirrhosis were superior to the results of sofosbuvir and velpatasvir tablets obtained in clinical studies in Asia (83% vs. 72%; 67% vs. 50%).

Coblopasvir hydrochloride capsule and sofosbuvir tablet were approved for marketing by National Medical Products Administration of China in Feb. 2020 and Mar. 2020, respectively. This study is designed to evaluate the safety and efficacy of coblopasvir hydrochloride capsules combined with sofosbuvir tablets in clinical practice after marketing.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    450 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Efficacy and Safety of Coblopasvir Hydrochloride Capsules Combined With Sofosbuvir Tablets for the Treatment of Chronic HCV Infection: A Prospective, Multi-center Real-world Study.
    Anticipated Study Start Date :
    Nov 1, 2022
    Anticipated Primary Completion Date :
    Dec 31, 2023
    Anticipated Study Completion Date :
    Dec 31, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Single Group Assignment

    Outcome Measures

    Primary Outcome Measures

    1. Sustained virologic response (SVR) [24 weeks]

      The proportion of patients with undetectable levels is detected by highly sensitive HCV RNA assay (lower limit of detection < 15 IU/mL)

    Secondary Outcome Measures

    1. Adverse events [24 weeks]

      Record AEs during the study (observe and record at any time).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Chronic hepatitis C infection

    2. Age 18 years and over

    3. Patients who treated with coblopasvir hydrochloride capsules/sofosbuvir tablets;

    Exclusion Criteria:
    1. Patients who are receiving other DAAs drugs at the same time;

    2. Subjects with poor compliance who are unable to complete treatment or follow-up.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bejing Tsinghua Changgung Hospital Beijing Bejing China 100015

    Sponsors and Collaborators

    • Beijing Tsinghua Chang Gung Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Beijing Tsinghua Chang Gung Hospital
    ClinicalTrials.gov Identifier:
    NCT05601518
    Other Study ID Numbers:
    • 22408-0-03
    First Posted:
    Nov 1, 2022
    Last Update Posted:
    Nov 1, 2022
    Last Verified:
    Oct 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Beijing Tsinghua Chang Gung Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 1, 2022