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NCT01567813

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

Completed Last updated 22 July 2022
What this trial tests

trial in Human Papilloma Virus Infection in 114,035 participants. Completed in 1 June 2019.

Timeline
23 June 2011
Primary endpoint
1 June 2019
1 June 2019

Quick facts

Lead sponsorMerck Sharp & Dohme LLC
StatusCompleted
Study typeOBSERVATIONAL
Enrollment114,035
Start date23 June 2011
Primary completion1 June 2019
Estimated completion1 June 2019

Conditions studied

Sponsor

Merck Sharp & Dohme LLC — full company profile →

Who can join

Adults 9 to 26, male only, with Human Papilloma Virus Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Human papillomavirus vaccination: a case study in translational science.
    Palmer AK, Harris AL, Jacobson RM. · · 2014 · cited 4× · PMID 24841923 · DOI 10.1111/cts.12166

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Other recruiting trials for Human Papilloma Virus Infection

Currently open trials in the same condition.

Other Merck Sharp & Dohme LLC trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01567813.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing