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Study identifier: NCT05266898 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Immunogenicity of Gardasil-9 HPV Vaccine in People Living With HIV

Condition: Papillomavirus Vaccines · Human Immunodeficiency Virus · Papillomavirus Infection  ·  Sponsor: Louisiana State University Health Sciences Center in New Orleans

PhasePhase 4
Planned participants250
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

The primary objective of this study is to determine the magnitude and breadth of the serum antibody response to the nonavalent HPV vaccine (Gardasil-9) in adults with well-controlled HIV infection. The secondary objectives of the study are to observe short term clinical outcomes of prevalent HPV genotype-specific anogenital infections in adults living with HIV who complete the three-dose Gardasil-9 vaccine series, and to determine the protection afforded by Gardasil vaccine over time in previously vaccinated adults living with HIV. The clinical hypothesis is that adults with virologically controlled HIV mount a serum antibody response to the nonavalent HPV vaccine that is comparable to HIV negative counterparts. We also postulate that HPV vaccination will provide short-term clinical benefit against HPV infections and disease associated with vaccine genotypes and continuing protection against vaccine genotypes of HPV over time.

This description comes directly from the study's public registry record.

Talk to the study team

Vice Chancellor for Academic Affairs and Research  ·  504-568-4804  ·  dporch@lsuhsc.edu

Executive Director, Office of Research Services  ·  504-568-4985  ·  jalam@lsuhsc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University Medical Center New OrleansNew Orleans, Louisiana, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05266898