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V502

Discontinued / Inactive

Developer: Merck Sharp & Dohme LLC  |  Target Disease: HPV

Program Status: Inactive / Discontinued

Reason: Registry status: WITHDRAWN

Stage at discontinuation: phase_2

Category Resource

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

View HPV Vaccine Guide →
Development Phase Discontinued / Inactive Primary Status
Platform Technology Biological (unspecified platform) Biologic Architecture
Target Indication HPV 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
Biological (unspecified platform)
Lead Developer
Merck Sharp & Dohme LLC
Next Expected Milestone
See linked ClinicalTrials.gov records for primary completion dates
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 NCT00365443 →

Registered Clinical Trials & Studies

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

NCT00365443 Discontinued / Inactive

Broad Spectrum HPV Vaccine Tolerability, Immunogenicity, and Efficacy Study (V502-003)

Status: Active / Ongoing • Expected Readout: TBD

Milestone Overview

  • Stage Verification
    Discontinued / Inactive confirmed as of 2026-07-10.
  • Target Milestone
    See linked ClinicalTrials.gov records for primary completion dates

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.