Effector and Memory Immune Responses to HPV Vaccination in Vietnamese Women Post Virus Exposure

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18-26
SponsorNational Institute of Hygiene and Epidemiology, Vietnam

About this trial

A Study to evaluate if the 3 dose extended schedule (0-6-18 months) for the HPV vaccine Gardasil-9 provide similar immune responses and short term protection against HPV infection compared to the regular 3 dose schedule (0-2-6 months) in high risk women in Vietnam

Eligibility criteria

Qualifiers

Is between the reporting ages of 18-26 years at the time of recruitment.

Engage in commercial sex in the last 6m (for FSW group) or have engaged in sexual activity (non-FSWs)

Willing and able to give written informed consent.

Willing to complete the follow-up requirements of the study.

Disqualifiers

Pregnant or possibly pregnant

Has received any HPV vaccine previously

Has an axillary temperate greater than 38°C

Known allergies to any vaccine component

Trial design

Treatments tested in this trial

  • Human papillomavirus 9-valent vaccine, Recombinant

Treatment groups

300 Participants
are divided into 3 treatment groups

Sponsors and collaborators

National Institute of Hygiene and Epidemiology, Vietnam

Lead sponsor

Murdoch Childrens Research Institute

Collaborator

CENTER FOR SUPPORTING COMMUNITY DEVELOPMENT INITIATIVES

Collaborator

Hai Phong Center for Disease Control

Collaborator