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Active Not RecruitingNCT04235257

Intradermal, Fractional Dose of HPV Vaccines:

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

Status
Active Not Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
University of Washington · Academic / Other
Sex
All
Age
27 Years – 45 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHPV vaccineGardasil 9 Bivalent HPV VLP Vaccine, one-fifth dose Nonavalent HPV VLP Vaccine, one-fifth dose

Timeline

Start date
2020-11-01
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2020-01-21
Last updated
2025-03-27

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04235257. Inclusion in this directory is not an endorsement.