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Active Not RecruitingNCT06989788

A Study to Evaluate the Safety and Immunogenicity of an Investigational Vaccine for Chronic Hepatitis B Virus Infection, in Healthy Adults

A Randomised, Double-blind, Placebo-controlled, Single Centre, Phase I Study to Evaluate the Safety, Reactogenicity and Immunogenicity of AstriVax' Investigational Therapeutic Hepatitis B Virus (HBV) Vaccine (AVX70371) in Healthy Adults Aged 18 to 40 Years

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
16 (estimated)
Sponsor
AstriVax Therapeutics · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this first time in humans trial is to evaluate the safety, reactogenicity and immunogenicity of repeated administrations of AVX70371 in healthy participants.

Conditions

Interventions

TypeNameDescription
BIOLOGICALAVX70371AstriVax Therapeutics' HBV immunotherapeutic
OTHERPlaceboPlacebo

Timeline

Start date
2025-05-06
Primary completion
2026-08-31
Completion
2026-08-31
First posted
2025-05-25
Last updated
2025-06-22

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT06989788. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Safety and Immunogenicity of an Investigational Vaccine for Chronic Hepatitis B Virus Infection, (NCT06989788) · Clinical Trials Directory