A Prospective, Multi-centre Post Marketing Surveillance (PMS) Cohort Study to Monitor the Safety of GlaxoSmithKline (GSK) Biologicals' Human Papillomavirus (HPV)-16/18 L1 VLP AS04 Vaccine in Female Chinese Subjects Aged Between 9 and 25 Years, When Administered According to the Prescribing Information (PI) as Per Routine Practice

Trial Profile

A Prospective, Multi-centre Post Marketing Surveillance (PMS) Cohort Study to Monitor the Safety of GlaxoSmithKline (GSK) Biologicals' Human Papillomavirus (HPV)-16/18 L1 VLP AS04 Vaccine in Female Chinese Subjects Aged Between 9 and 25 Years, When Administered According to the Prescribing Information (PI) as Per Routine Practice

Recruiting
Phase of Trial: Phase IV

Latest Information Update: 13 Aug 2018

At a glance

  • Drugs Human papillomavirus vaccine recombinant bivalent Japan Vaccine/MedImmune (Primary)
  • Indications Cervical cancer; Cervical intraepithelial neoplasia; Human papillomavirus infections
  • Focus Adverse reactions
  • Sponsors GlaxoSmithKline
  • Most Recent Events

    • 02 Aug 2018 Status changed from not yet recruiting to recruiting.
    • 05 Jun 2018 Planned initiation date changed from 11 Jun 2018 to 31 May 2018.
    • 08 Mar 2018 Planned End Date changed from 30 Dec 2020 to 14 Mar 2021.
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