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Clinical Trial Summary

The purpose of this study is to evaluate the tolerability, and pharmacokinetics of AHB-137 subcutaneous injection in healthy participants after single and multiple doses. In addition, the study will evaluate the antiviral efficacy of AHB-137 in chronic hepatitis B (CHB) patients following a multiple dosing regimen.


Clinical Trial Description

This study is a two-part study of AHB-137, including Part Ia and Part Ib. Part Ia evaluates the tolerability, pharmacokinetics of AHB-137 following subcutaneous single-ascending doses (SAD) or multiple-ascending doses (MAD) in healthy volunteers. Part Ib is a multiple dose study to assess the safety, tolerability, pharmacokinetics, and antiviral efficacy of AHB-137 in chronic hepatitis B (CHB) patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06115993
Study type Interventional
Source Ausper Biopharma Co., Ltd.
Contact Bella Lu
Phone +8615968607969
Email bingxia.lu@ausperbio.com
Status Recruiting
Phase Phase 1
Start date August 3, 2023
Completion date October 2024

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