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NCT06159062

A Clinical Study of 162 in Subjects With Chronic Hepatitis B Virus Infection

Terminated Phase 1 Last updated 16 July 2024
What this trial tests

Phase 1 trial testing 162 in Chronic Hepatitis B Virus Infection in 1 participant. Terminated before completion.

Timeline
3 June 2024
Primary endpoint
9 July 2024
9 July 2024

Quick facts

Lead sponsorYangshengtang Co., Ltd
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment1
Start date3 June 2024
Primary completion9 July 2024
Estimated completion9 July 2024
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Yangshengtang Co., Ltd

Who can join

Adults 18 to 65, any sex, with Chronic Hepatitis B Virus Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this intervention research is to learn about the safety and tolerability of 162 with a single ascending dose in subjects with chronic hepatitis B virus (HBV) infection.

Publications & conference data

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

  1. The significance of antibody to hepatitis B surface antigen in infection and clearance of hepatitis B virus.
    Ding L, Huang J, Huang S. · · 2025 · cited 3× · PMID 39754388 · DOI 10.1080/21645515.2024.2445283

Verify or expand the search:

Other trials of 162

Trials testing the same drug.

Other recruiting trials for Chronic Hepatitis B Virus Infection

Currently open trials in the same condition.

Other Yangshengtang Co., Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing