Trial intelligence / Profile preview

Immunogenicity and Safety of Cervarix in Healthy Females Aged 15-25 Years

NCT00485732Phase 3Completed

Sponsor
GSK
Start
Jun 2007
Primary completion
Mar 2008
Modality
Vaccines & Immunotherapeutics
Countries
1
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Overview

Phase 3, randomised, double-blind trial in human papillomavirus infection comparing Cervarix Group with Placebo Group (2 arms). Primary endpoint: Number of Subjects Seroconverted for Anti-human Papilloma Virus 16 (Anti-HPV-16) and Anti-human Papilloma Virus 18 (Anti-HPV-18) Antibodies at Month 7. Started Jun 2007; status: completed.

02

Drugs

Human papillomavirus type 16 L1 capsid protein residues 2-471 antigen
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Conditions

human papillomavirus infection

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