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RECRUITING
NCT05495906
PHASE4

A Study of Reduced Dosing of the Nonavalent HPV Vaccine in Women Living With HIV

Sponsor: University of British Columbia

View on ClinicalTrials.gov

Summary

There are very little data on human papillomavirus (HPV) vaccination among the 18 million women living with HIV (WLWH) globally, who constitute a population most vulnerable to HPV and the resultant cervical cancer. Particularly, there are no data to date on reduced-dose schedules of nonavalent HPV (9vHPV) vaccination in WLWH and there are very little data on the 9vHPV vaccine in this population overall. It is critical to examine the 9vHPV vaccine in WLWH now because the quadrivalent HPV (4vHPV) vaccine has been discontinued. Additionally, in order to reach the World Health Organization's global goal of cervical cancer elimination, we must determine the role of various HPV prevention strategies in this important population including reduced vaccine dosing which can drastically increase the feasibility of HPV vaccination programs globally. This randomized clinical trial will enrol WLWH aged 18-45 from across Canada who have not previously received an HPV vaccine. Participants will be randomized 1:1 to receive 3 doses of 9vHPV vaccine at the routine vaccine schedule of 0/2/6 months or 2 doses at an expanded schedule of 0/6 months with a third dose at month 12 to adhere to current recommendations for WLWH. We will compare the immune response generated to two versus three doses of 9vHPV vaccine and will follow participants for 2 years to examine the immune response over time. This study, which builds upon our team's prior work on HPV vaccination in WLWH, will determine whether two doses of 9vHPV vaccine can be used in WLWH instead of three, and will examine additional aspects of HPV vaccination in WLWH including the immune response to three doses, vaccine safety and efficacy, and attitudes towards self-collected HPV samples in this population. These data will inform global public health policy and programming and will inform the global strategy for cervical cancer elimination.

Key Details

Gender

FEMALE

Age Range

18 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

275

Start Date

2023-07-27

Completion Date

2028-01

Last Updated

2026-02-05

Healthy Volunteers

Yes

Interventions

BIOLOGICAL

Nonavalent HPV vaccine

Routine dosing form and dosage

Locations (10)

Positive Health Services - Fraser Health

Surrey, British Columbia, Canada

University of British Columbia

Vancouver, British Columbia, Canada

Health Sciences Centre

Winnipeg, Manitoba, Canada

Hamilton Health Sciences

Hamilton, Ontario, Canada

St. Michael's Hospital

Toronto, Ontario, Canada

Toronto General Hospital

Toronto, Ontario, Canada

Centre Hospitalier Universitaire Sainte-Justine

Montreal, Quebec, Canada

McGill University Health Centre

Montreal, Quebec, Canada

Centre Hospitalier de l'Université Laval

Québec, Quebec, Canada

Regina General Hospital

Regina, Saskatchewan, Canada