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NCT05376124

Clinical Characteristics, Natural Outcome and Treatment Optimization of Refractory

Status unknown Last updated 3 February 2023
What this trial tests

trial testing original therapy in Hepatitis B, Chronic in 110 participants. Status unknown.

Timeline
1 January 2022
Primary endpoint
31 December 2024
31 December 2025

Quick facts

Lead sponsorFirst Affiliated Hospital Xi'an Jiaotong University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment110
Start date1 January 2022
Primary completion31 December 2024
Estimated completion31 December 2025
Sites13 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

First Affiliated Hospital Xi'an Jiaotong University

Who can join

Adults 18 to 70, any sex, with Hepatitis B, Chronic or Virus Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Refractory hepatitis B is to point to although standard application nucleoside (acid) analogue treatment undertakes primary treatment and two strengthen treatment, but existence is persistent viremia. Currently, there is no consensus on salvage therapy for patients who remain virus-positive after a second round of antiviral therapy. This is the first multicenter, prospective, parallel controlled, open-label cohort study to compare the efficacy and safety of TDF/TAF combined with ETV1.0mg regimen versus continuation of the original regimen in the treatment of refractory hepatitis B.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hepatitis B, Chronic

Currently open trials in the same condition.

Other First Affiliated Hospital Xi'an Jiaotong University 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/NCT05376124.

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