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Cervarix Immunogenicity and Safety in Healthy Indian Women
NCT00344032Phase 3Completed
- Sponsor
- GSK
- Start
- Jul 2006
- Primary completion
- Dec 2007
- Modality
- Vaccines & Immunotherapeutics
- Countries
- 1
01
Overview
Phase 3, randomised, double-blind trial in human papillomavirus infection comparing Cervarix with Placebo (2 arms). Primary endpoint: Number of Subjects Who Seroconverted for Anti-human Papilloma Virus 16 and 18 Antibodies at Month 7. Started Jul 2006; status: completed.
02
Drugs
Human papillomavirus type 16 L1 capsid protein residues 2-471 antigen
03
Conditions
human papillomavirus infection
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