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Two-dose Schedule of Quadrivalent HPV Recombinant Vaccine in 11-year-old Boys in Mexico City

Primary Purpose

Human Papilloma Virus

Status
Unknown status
Phase
Phase 3
Locations
Mexico
Study Type
Interventional
Intervention
quadrivalent human papillomavirus (types 6, 11, 16,18) recombinant vaccine
Sponsored by
Universidad Nacional Autonoma de Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Human Papilloma Virus focused on measuring quadrivalent, vaccine

Eligibility Criteria

10 Years - 11 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • All those children whose parents accept their participation in the study.

Exclusion Criteria:

  • Fever,
  • previous vaccination against HPV,
  • allergy to vaccine components,
  • thrombocytopenia,
  • immunosuppression,
  • diarrhea,
  • vomiting,
  • dyscrasia,
  • administration of another anti-viral vaccine in the previous 15 days.

Sites / Locations

  • Malaquias Lopez CervantesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Cohort 1

Cohort 2

Cohort 3

Arm Description

11 year old boys enrolled in fifth grade of 40 public elementary schools of Mexico City, from the political demarcations of Azcapotzalco, Gustavo A. Madero, Iztacalco, Miguel Hidalgo, Venustiano Carranza, Iztacalco and Tlalpan, reciving a two-dose vaccination scheme (0-6). 250 subjects will be recruited.

Historical cohort of young women 18-24 years old recruited by Lazcano et. al. receiving a standard vaccination schedule (0-1-6 months). 500 subjects were recruited.

11 year old girls enrolled in fifth grade of 40 public elementary schools of Mexico City, from the political demarcations of Azcapotzalco, Venustiano Carranza, Iztacalco and Tlalpan, reciving a two-dose vaccination scheme (0-6). 250 subjects will be recruited.

Outcomes

Primary Outcome Measures

Immunogenicity (Geometric mean antibody concentration will be compared between the two groups)
Geometric means will be compared between the two groups of interest (boys and young women)

Secondary Outcome Measures

Full Information

First Posted
March 3, 2015
Last Updated
March 6, 2015
Sponsor
Universidad Nacional Autonoma de Mexico
Collaborators
Merck Sharp & Dohme LLC, Secretaria de Salud, Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT02382900
Brief Title
Two-dose Schedule of Quadrivalent HPV Recombinant Vaccine in 11-year-old Boys in Mexico City
Official Title
Evaluation of a Two-dose Schedule of Quadrivalent Human Papilloma Virus (Types 6, 11, 16, 18) Recombinant Vaccine in 11-year-old Boys in Mexico City (Gardasil® Merck and Co.).
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
October 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Nacional Autonoma de Mexico
Collaborators
Merck Sharp & Dohme LLC, Secretaria de Salud, Mexico

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In the genital tract human papilloma virus (HPV), especially types 6 and 11 cause genital warts, the commonest viral sexually transmitted disease. The HPV 16 and 18 are the most common oncogenic "high-risk" genotypes and cause approximately 70% of all cervical cancers despite the fact that are associated with other anogenital cancers, anus, vagina, vulva and penis, and cancers of the head and neck. Current estimates are that 5.2% of all cancers are HPV associated. A large number of studies, including both adult and young females, have demonstrated that HPV vaccines are highly immunogenic and induce a long lasting protection against infection. Immunogenic vaccination results in young men and boys are equally satisfactory with the quadrivalent HPV (types 6, 11, 16, 18) vaccine recommended for men. The recommended vaccination scheme includes three shots giving the second at two months and the third at six months after the initial shot. Recently, it has been shown that the use of a two shot scheme (0 and 6 months) is equally effective among girls. The purpose of this study is to determine that the immunogenicity is non-inferior in boys using a two shot scheme compared with young women and girls.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Papilloma Virus
Keywords
quadrivalent, vaccine

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cohort 1
Arm Type
Experimental
Arm Description
11 year old boys enrolled in fifth grade of 40 public elementary schools of Mexico City, from the political demarcations of Azcapotzalco, Gustavo A. Madero, Iztacalco, Miguel Hidalgo, Venustiano Carranza, Iztacalco and Tlalpan, reciving a two-dose vaccination scheme (0-6). 250 subjects will be recruited.
Arm Title
Cohort 2
Arm Type
Active Comparator
Arm Description
Historical cohort of young women 18-24 years old recruited by Lazcano et. al. receiving a standard vaccination schedule (0-1-6 months). 500 subjects were recruited.
Arm Title
Cohort 3
Arm Type
Active Comparator
Arm Description
11 year old girls enrolled in fifth grade of 40 public elementary schools of Mexico City, from the political demarcations of Azcapotzalco, Venustiano Carranza, Iztacalco and Tlalpan, reciving a two-dose vaccination scheme (0-6). 250 subjects will be recruited.
Intervention Type
Biological
Intervention Name(s)
quadrivalent human papillomavirus (types 6, 11, 16,18) recombinant vaccine
Other Intervention Name(s)
Gardasil
Intervention Description
dose scheme (0 and 6 month)
Primary Outcome Measure Information:
Title
Immunogenicity (Geometric mean antibody concentration will be compared between the two groups)
Description
Geometric means will be compared between the two groups of interest (boys and young women)
Time Frame
7 months (1 month after the last dose)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All those children whose parents accept their participation in the study. Exclusion Criteria: Fever, previous vaccination against HPV, allergy to vaccine components, thrombocytopenia, immunosuppression, diarrhea, vomiting, dyscrasia, administration of another anti-viral vaccine in the previous 15 days.
Facility Information:
Facility Name
Malaquias Lopez Cervantes
City
Mexico
State/Province
Mexico city
ZIP/Postal Code
04510
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Malaquias Lopez, Ph. D.
Phone
+525556232427
Email
mlopez14@unam.mx
First Name & Middle Initial & Last Name & Degree
Reyna Lizette Pacheco, Dr. Sc.
Phone
+525556232373
Email
lirey@unam.mx

12. IPD Sharing Statement

Learn more about this trial

Two-dose Schedule of Quadrivalent HPV Recombinant Vaccine in 11-year-old Boys in Mexico City

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