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Clinical Trial Summary

This is a multicenter study in which women are planned to receive either the HPV vaccine or control. Study participation will last approximately 72 months and involves a total of thirteen or fourteen scheduled visits.

Originally, the study was planned for 24 months. It was then extended for 2 more years with 4 additional visits (study end at Month 48).

The protocol posting has been updated as the study was extended by additional 2 years with two or three additional visits (study end at Month 72) for subjects who consent to participate in the extension.


Clinical Trial Description

This protocol posting has been updated following protocol amendment 6 dated 24 April 2014. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00779766
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 3
Start date October 22, 2008
Completion date February 28, 2016

See also
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