drugset / Trial / NCT06115993

A Study to Evaluate the Safety and Efficacy of AHB-137 in Healthy Participants and HBeAg-negative Chronic Hepatitis B (CHB) Patients

NCT06115993

Phase 1/2 Completed 129 enrolled Ausper Biopharma Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of AHB-137 subcutaneous injection in healthy participants after single and multiple doses, and evaluate the preliminary efficacy of AHB-137 in CHB participants after up to 24 weeks of treatment as a proof-of-concept.

Timeline

Start
2023-08-03
Primary completion
2024-12-03
Completion
2025-11-10

Drugs

EvaluationDrugModalityDoseRoute
Subject AHB-137 Antisense oligonucleotide 75 mg Subcutaneous
Subject AHB-137 Antisense oligonucleotide 150 mg Subcutaneous
Subject AHB-137 Antisense oligonucleotide 225 mg Subcutaneous
Subject AHB-137 Antisense oligonucleotide 300 mg Subcutaneous
Subject AHB-137 Antisense oligonucleotide 450 mg Subcutaneous