drugset / Trial / NCT07519330
Clinical Study to Evaluate the Efficacy and Safety of HH-006 in Patients With Chronic Hepatitis B Virus Infection
Non-randomizedSingle-groupOpen-labelTreatment
Summary
Study HH006-202 is designed to assesses the efficacy and safety of HH-006 in adults chronic HBV infection. Eligible participants will receive study treatment for 48 weeks. All treated patients will also undergo a follow-up period after last study drug treatment.
Timeline
- Start
- 2026-05-14
- Primary completion
- 2028-02-28
- Completion
- 2028-03-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HH-006 | Monoclonal antibody | 240 mg | Subcutaneous |