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A Phase III Clinical Trial to Study the Tolerability and Immunogenicity of a 2-dose Regimen of V503, a Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine, Administered in Preadolescents and Adolescents (9 to 14 Year Olds) With a Comparison to Young Women (16 to 26 Year Olds)

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Trial Profile

A Phase III Clinical Trial to Study the Tolerability and Immunogenicity of a 2-dose Regimen of V503, a Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine, Administered in Preadolescents and Adolescents (9 to 14 Year Olds) With a Comparison to Young Women (16 to 26 Year Olds)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 13 May 2022

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At a glance

  • Drugs V 503 (Primary)
  • Indications Human papillomavirus infections
  • Focus Pharmacodynamics; Registrational
  • Sponsors Merck & Co; Merck Sharp & Dohme Corp.

Most Recent Events

  • 01 Jan 2021 Results published in the Pediatrics
  • 28 Jul 2017 Status changed from active, no longer recruiting to completed.
  • 22 Jun 2017 Planned End Date changed from 16 Jun 2017 to 3 Aug 2017.

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