A PHASE III CLINICAL TRIAL TO STUDY THE TOLERABILITY AND IMMUNOGENICITY OF A 2-DOSE REGIMEN OF V503, A MULTIVALENT HUMAN PAPILLOMAVIRUS (HPV) L1 VIRUS-LIKE PARTICLE (VLP) VACCINE, ADMINISTERED IN PREADOLESCENTS AND ADOLESCENTS (9 TO 14 YEAR OLDS) WITH …

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE III CLINICAL TRIAL TO STUDY THE TOLERABILITY AND IMMUNOGENICITY OF A 2-DOSE REGIMEN OF V503, A MULTIVALENT HUMAN PAPILLOMAVIRUS (HPV) L1 VIRUS-LIKE PARTICLE (VLP) VACCINE, ADMINISTERED IN PREADOLESCENTS AND ADOLESCENTS (9 TO 14 YEAR OLDS) WITH A COMPARISON TO YOUNG WOMEN (16 TO 24 YEAR OLDS)

Intervention/treatment:
V503 (NONAVALENT HPV L1 VLP VACCINE)
Medical condition:
HUMAN PAPILLOMA VIRUS (HPV)
Protocol code:
010-00
Control number:
168341
Status:
No match, ongoing
Approved:
October 17, 2013
Trial phase:
Other
For more information:
No registry match found

Eligibility

Sex: ALL
Age

Contacts and locations

Contact
Sponsor
MERCK CANADA INC
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