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A Phase 1/2 Randomized, Observer-blinded, Multi-country Study to Evaluate Safety and Immunogenicity of Investigational Adjuvanted Human Papillomavirus Vaccine in Females (16 to 26 Years of Age)

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Trial Profile

A Phase 1/2 Randomized, Observer-blinded, Multi-country Study to Evaluate Safety and Immunogenicity of Investigational Adjuvanted Human Papillomavirus Vaccine in Females (16 to 26 Years of Age)

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 10 Feb 2025

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At a glance

  • Drugs Human-papillomavirus-adjuvanted-vaccine-GlaxoSmithKline/Xiamen-Innovax-Biotech (Primary) ; V 503
  • Indications Cervical intraepithelial neoplasia
  • Focus Adverse reactions; First in man; Pharmacodynamics
  • Acronyms HPV9-AS04-001
  • Sponsors GlaxoSmithKline; GlaxoSmithKline Biologicals; GSK
  • Most Recent Events

    • 03 Feb 2025 Primary endpoints updated.
    • 13 Nov 2024 Status changed from active, no longer recruiting to completed.
    • 25 May 2024 This trial has been completed in Poland (Global end date: 23 Feb 2024).

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