Post-Licensure Study of the Safety of GARDASIL™ in Males (V501-070)

NCT01567813 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 114035

Last updated 2022-07-22

No results posted yet for this study

Summary

This is a post-licensure safety observation cohort study to describe the general safety of GARDASIL™ (a quadrivalent human papillomavirus vaccine) in males.

Conditions

  • Human Papilloma Virus Infection

Sponsors & Collaborators

Eligibility

Min Age
9 Years
Max Age
26 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-06-23
Primary Completion
2019-06-01
Completion
2019-06-01

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01567813 on ClinicalTrials.gov