drugset / Trial / NCT04270773

Immunogenicity and Safety of a 9-valent Human Papillomavirus Vaccine in HIV-positive Women

NCT04270773

NaSingle-groupOpen-labelTreatment

Summary

In adult HIV-positive patients, data on the safety and immunogenicity of the quadrivalent HPV (qHPV) vaccine have been reported with excellent results (13 14); also, the results of a clinical trial of qHPV vaccine conducted in seropositive patients older than 36 years (WLHIV and MSM) have been published. Even now, there is not a trial about immunogenicity and safety of a 9-valent human papillomavirus vaccine in HIV-positive women; for this reason, the investigators plan to conduct this clinical trial. HYPOTHESYS: The administration of Nonavalent HPV vaccine (HPV-9) in adult women living with HIV will produce antibodies against nine genotypes of HPV, thus preventing the acquisition of new infections by those genotypes. Besides, this will prevent the cervical and anal dysplasia in these women.

Timeline

Start
2020-02-12
Primary completion
2024-09-30
Completion
2024-12-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Gardasil 9 Vaccine