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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |