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Evaluating the Immunogenicity and Safety of Quadrivalent Human Papillomavirus Recombinant Vaccine (Type 6, 11, 16, 18) in Healthy Chinese Female Subjects Aged 9 to 26 Years: A Phase 3, Open-label, Non-randomized Clinical Trial

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Trial Profile

Evaluating the Immunogenicity and Safety of Quadrivalent Human Papillomavirus Recombinant Vaccine (Type 6, 11, 16, 18) in Healthy Chinese Female Subjects Aged 9 to 26 Years: A Phase 3, Open-label, Non-randomized Clinical Trial

Status: Recruiting
Phase of Trial: Phase III

Latest Information Update: 22 Apr 2024

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At a glance

  • Drugs Human papillomavirus vaccine recombinant quadrivalent Merck (Primary)
  • Indications Anal cancer; Anal intraepithelial neoplasia; Cervical cancer; Condylomata acuminata; Human papillomavirus infections; Penile cancer
  • Focus Pharmacodynamics; Registrational
  • Sponsors Shanghai Bovax Biotechnology

    • Most Recent Events

    • 23 Feb 2022 Planned number of patients changed from 1350 to 1348.
    • 23 Feb 2022 Status changed from not yet recruiting to recruiting.
    • 06 Sep 2021 New trial record

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