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ACTIVE NOT RECRUITING
NCT05291871
PHASE4
Immunogenicity of Fractional Dose of the HPV Vaccines
Sponsor: University of Washington
View on ClinicalTrials.gov
Summary
This randomized phase IV trial compares intramuscular and intradermal fractional dose of bivalent HPV vaccine to fractional dose of nonavalent HPV vaccine among men and women aged 27-45 years in Seattle, Washington. Participants will have immune response assessed at baseline, 4 weeks, 6 months, and 12 months
Key Details
Gender
All
Age Range
27 Years - 45 Years
Study Type
INTERVENTIONAL
Enrollment
92
Start Date
2022-06-15
Completion Date
2026-12-31
Last Updated
2025-03-27
Healthy Volunteers
Yes
Conditions
Interventions
BIOLOGICAL
HPV vaccine
One-fifth dose bivalent HPV Vaccine or One-fifth dose nonavalent HPV Vaccine
Locations (1)
University of Washington Virology Research Clinic
Seattle, Washington, United States