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Clinical Trial Summary

To prove that quadrivalent HPV (types 6, 11, 16, 18) L1 virus-like particle (VLP) vaccine is generally safe and well tolerated in the Chinese population.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00635830
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 1
Start date March 2008
Completion date April 2008

See also
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Recruiting NCT05027776 - Immunogenicity and Safety of Quadrivalent HPV Vaccine in Healthy Chinese Female Subjects Aged 9 to 19 Years Phase 3
Suspended NCT00733122 - Tolerability and Immunogenicity of Gardasil in Females Between 16 and 23 Years of Age in India (V501-034) Phase 3
Recruiting NCT04895020 - Immunobridging Study of 9-valent Human Papillomavirus Recombinant Vaccine in Chinese Females Aged 9 to 19 Years Phase 3
Recruiting NCT05371353 - Immune Persistence After the Whole Vaccination Shcedule With Recombination Quadrivalent HPV Vaccine
Completed NCT03900572 - A Study of Safety and Primary Immunogenicity of 9-valent HPV Recombinant Vaccine Phase 1
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Completed NCT00378560 - V501 Efficacy Study in Women Aged 18 to 26 (V501-027) Phase 2
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Completed NCT00411749 - V501 Immunogenicity Study in Females Age 9 to 17 Years (V501-028) Phase 2
Completed NCT00943722 - A Study of V503 (A Multivalent Human Papillomavirus [HPV] L1 Virus-Like Particle [VLP] Vaccine) in Preadolescents and Adolescents (V503-002) Phase 3