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NCT01567813
Post-Licensure Study of the Safety of GARDASIL™ in Males (V501-070)
trial in Human Papilloma Virus Infection in 114,035 participants. Completed in 1 June 2019.
1 June 2019
Quick facts
| Lead sponsor | Merck Sharp & Dohme LLC |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 114,035 |
| Start date | 23 June 2011 |
| Primary completion | 1 June 2019 |
| Estimated completion | 1 June 2019 |
Conditions studied
- Human Papilloma Virus Infection — all drugs for Human Papilloma Virus Infection →
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):
-
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
Verify or expand the search:
- PubMed search for NCT01567813
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Human Papilloma Virus Infection
Currently open trials in the same condition.
- NCT06467942 — Effects of Chinese Medicine and Lactobacillus in Persistent HPV Infection · NA · recruiting
Other Merck Sharp & Dohme LLC trials
Trials by the same sponsor.
- NCT07224477 — A Clinical Study of V540A in Healthy Female Participants (V540A-005) · Phase 2 · not yet recruiting
- NCT07302347 — A Study of Pembrolizumab in Japanese Pediatric Participants With Solid Tumors or Lymphomas and Japanese Adult Participan · Phase 1, PHASE2 · recruiting
- NCT07528508 — A Clinical Trial in Healthy Participants to Study the Effect of a Single Dose of MK-8527 on Levels of Methadone (MK-8527 · Phase 1 · not yet recruiting
- NCT07513376 — A Clinical Trial of Adjuvant Intismeran (V940) With or Without Pembrolizumab Coformulated With Berahyaluronidase Alfa (M · Phase 3 · not yet recruiting
- NCT07532304 — A Clinical Trial of MK-4646 With Bictegravir/Emtricitabine/Tenofovir Alafenamide and Dolutegravir in Healthy Adult Parti · Phase 1 · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT01567813 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Merck Sharp & Dohme LLC
- Last refreshed: 22 July 2022
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