3-year Immunogenicity Evaluation of Quadrivalent HPV Vaccine in China

NCT01427777 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2011-09-02

No results posted yet for this study

Summary

The thirty-six-month immunogenicity evaluation of Quadrivalent HPV (Types 6, 11, 16, 18) L1 Virus-Like Particle (VLP) Vaccine in Chinese female subjects aged 9 to 45 years and male subjects aged 9 to 15 years.

Conditions

  • Anogenital Human Papilloma Virus Infection

Sponsors & Collaborators

  • Guangxi Center for Disease Control and Prevention

    lead OTHER_GOV

Principal Investigators

  • Rongcheng Li, MD · Guangxi CDC

Eligibility

Min Age
9 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-09-30
Completion
2012-06-30

Countries

  • China

Study Locations

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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 NCT01427777 on ClinicalTrials.gov