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Intradermal, Fractional Dose of HPV Vaccines:

HPV Infection Clinical Trial

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

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04235257
Study type Interventional
Source University of Washington
Contact
Status Active, not recruiting
Phase Phase 4
Start date November 1, 2020
Completion date December 31, 2024
View Details
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