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ACTIVE NOT RECRUITING
NCT04235257
PHASE4

Intradermal, Fractional Dose of HPV Vaccines:

Sponsor: University of Washington

View on ClinicalTrials.gov

Summary

This randomized phase IV trial compares 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, 12 months, and 24 months.

Official title: Immunogenicity of Fractional Dose of the Bivalent and Nonavalent Intradermal HPV Vaccines.

Key Details

Gender

All

Age Range

27 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2020-11-01

Completion Date

2026-12-31

Last Updated

2025-03-27

Healthy Volunteers

Yes

Interventions

BIOLOGICAL

HPV vaccine

Gardasil 9 Bivalent HPV VLP Vaccine, one-fifth dose Nonavalent HPV VLP Vaccine, one-fifth dose

Locations (1)

University of Washington Virology Research Clinic

Seattle, Washington, United States