Papillomavirus Vaccines Clinical Trial
Official title:
Complementary Testing to Further Evaluate the Immunogenicity of a GSK Biologicals' HPV Vaccine (580299) in Healthy Female Subjects Aged Over 26 Years Enrolled in Study 104820.
Infection with human papillomavirus (HPV) has been clearly established as the central cause
of cervical cancer. Indeed, certain oncogenic types of HPV can infect the cervix (part of
the uterus or womb). This infection may go away by itself, but if it does not go away (this
is called persistent infection), it can lead in women over a long period of time to cancer
of the cervix. This study will supplement an ongoing study evaluating the safety, efficacy
and immunogenicity of the vaccine in women aged 26 years and above. This study will
therefore assess additional immunogenicity parameters of the vaccine in women from selected
investigative sites.
The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep
2007.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
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