Clinical trial
A Phase III Open-Label Clinical Trial to Study the Immunogenicity and Tolerability of V503, a Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine, Given Concomitantly With REPEVAX™ in Preadolescents and Adolescents (11 to 15 Year Olds)
NCT01073293 is registered in ClinicalTrials.gov with Merck Sharp & Dohme LLC as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase III Open-Label Clinical Trial to Study the Immunogenicity and Tolerability of V503, a Multivalent Human Papillomavirus (HPV) L1 Virus-Like Particle (VLP) Vaccine, Given Concomitantly With REPEVAX™ in Preadolescents and Adolescents (11 to 15 Year Olds)
- Lead sponsor
- Merck Sharp & Dohme LLC
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- April 22, 2010
- Completion date
- June 16, 2011
- Enrollment
- 1,054 (actual)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.