drugset / Trial / NCT04820686
A Study Evaluating Treatment Regimens Containing Vebicorvir (ABI-H0731) in Participants With Chronic Hepatitis B Infection
RandomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to determine if vebicorvir (VBR, ABI-H0731) in combination with AB-729 is safe and effective in participants with chronic hepatitis B infection (cHBV) receiving a standard of care nucleos(t)ide/reverse transcriptase inhibitor (SOC NrtI).
Timeline
- Start
- 2021-05-07
- Primary completion
- 2023-03-30
- Completion
- 2023-03-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Imdusiran | Small interfering RNA (siRNA) | 60 mg | Subcutaneous |
| Subject | VBR | Unknown | 300 mg | Oral |
| Background | Entecavir | Small molecule | — | Oral |
| Background | Tenofovir disoproxil fumarate | Small molecule | — | Oral |
| Background | tenofovir alafenamide | Small molecule | — | Oral |