drugset / Trial / NCT06159062

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

NCT06159062 ↗

Phase 1 Terminated 1 enrolled Yangshengtang Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2024-06-03
Primary completion
2024-07-09
Completion
2024-07-09

Outcome

Outcome not reported

Stopped (Enrollment): “Enrollment difficulty”

Drugs

EvaluationDrugModalityDoseRoute
Subject 162 Monoclonal antibody 50 mg —
Subject 162 Monoclonal antibody 75 mg —
Subject 162 Monoclonal antibody 100 mg —