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Active Not RecruitingNCT07204236

Study to Evaluate Immunogenicity and Safety of TVAX-008 Injection in Non/Treated Chronic Hepatitis B Patients With HBsAg≤20IU/ml or HBsAg Negative Without Serological Conversion

Status
Active Not Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Grand Theravac Life Sciences (Nanjing) Co., Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to assess the immunogenicity and safety of TVAX-008 injection in antiviral untreated/untreated chronic hepatitis B patients with HBsAg≤20 IU/mL, or HBsAg negative and no seroconversion through an investigator-initiated clinical study.

Conditions

Interventions

TypeNameDescription
DRUGTVAX-008TVAX-008

Timeline

Start date
2024-01-18
Primary completion
2025-03-01
Completion
2026-03-01
First posted
2025-10-02
Last updated
2025-10-02

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07204236. Inclusion in this directory is not an endorsement.

Study to Evaluate Immunogenicity and Safety of TVAX-008 Injection in Non/Treated Chronic Hepatitis B Patients With HBsAg (NCT07204236) · Clinical Trials Directory