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MVA-HBV low dose formulation

Discontinued / Inactive

Developer: GlaxoSmithKline  |  Target Disease: Hepatitis B

Program Status: Inactive / Discontinued

Reason: Registry status: TERMINATED

Stage at discontinuation: phase_2

Category Resource

Explore licensed vaccines, adverse event reporting data, and history for this disease.

View Hepatitis B Vaccine Guide →
Development Phase Discontinued / Inactive Primary Status
Platform Technology Viral vector Biologic Architecture
Target Indication Hepatitis B Pathogen / Antigen
Last Verified 2026-07-10 Tier 1 Multi-Source Checked

Multi-Jurisdiction Regulatory Status

Official licensing, rolling submissions, or authorization status tracked across major health authorities.

Regulatory Authority Status & Details
US FDA Not Filed / Pre-submission
EMA (Europe) Not Filed / Pre-submission
Health Canada Not Filed / Pre-submission
TGA (Australia) Not Filed / Pre-submission

Scientific Profile & Documentation

Platform Architecture
Viral vector
Lead Developer
GlaxoSmithKline
Next Expected Milestone
Primary completion (most advanced trial): 2024-10-07 (registry estimate)
Analyst & Development Notes
Auto-grouped from 1 ClinicalTrials.gov record(s) sharing intervention/sponsor. Phases and timelines are registry fields and may lag company disclosures.
Primary Source Documentation
ClinicalTrials.gov NCT03866187 →

Registered Clinical Trials & Studies

Direct registry links to active, completed, or pivotal registration studies across phases.

NCT03866187 Discontinued / Inactive

Safety, Efficacy, Immunogenicity Study of GSK Biologicals' HBV Viral Vector and Adjuvanted Proteins Vaccine (GSK3528869A

Status: Active / Ongoing • Expected Readout: 2024-10-07

Milestone Overview

  • Stage Verification
    Discontinued / Inactive confirmed as of 2026-07-10.
  • Target Milestone
    Primary completion (most advanced trial): 2024-10-07 (registry estimate)

Vaccine Data Navigator Candidate Profile Registry:

This candidate profile is indexed across all clinical development levels (Preclinical through Phase 1–3, Regulatory Filing, and Licensure) from primary registry databases (ClinicalTrials.gov, WHO ICTRP, FDA CBER, EMA, Health Canada, TGA Australia). Data are updated continuously to track global biologic and vaccine pipelines.