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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03431246
Other study ID # CÉ: 2017-3036-21
Secondary ID
Status Completed
Phase Phase 3
First received January 26, 2018
Last updated February 6, 2018
Start date October 1, 2016
Est. completion date December 5, 2016

Study information

Verified date February 2018
Source Laval University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will assess the immunogenicity of one dose of Gardasil and one dose of Gardasil-9


Description:

This is a one group exploratory study.

The main objective of this study is to assess the persistance of anti-HPV after a single dose Gardasil and the effect of one dose of Gardasil-9 when administered 3-8 years later.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date December 5, 2016
Est. primary completion date November 5, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria: Have received a single dose of Gardasil 3-8 years before recruitement.

Exclusion Criteria: Immunossupressed or blood coagulation problems

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Gardasil and Gardasil-9
All subjects will receive one dose of Gardasil-9. Blodd samples for serological testing will be collected just before and one month post Gardasil-9 administration.

Locations

Country Name City State
Canada Laval University Research Hospital Center Quebec

Sponsors (2)

Lead Sponsor Collaborator
Laval University Centers for Disease Control and Prevention

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anti-HPV seropositivity Seropositivity to 9 HPV types included in Gardasil-9 vaccine will be assessed. One month post vaccine administration.
Secondary HPV antibody titers Geometrical mean titers of antibodies to 9 HPV types included in Gardasil-9 vaccine will be assessed One month post vaccine administration
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