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Clinical Trial Summary

The purpose of this study is to evaluate the immunogenicity and the safety of Cervarix administered according to a 2-dose schedule at 0, 6 months compared to Gardasil, administered according to a 2-dose schedule at 0, 6 months or the standard 3-dose schedule of 0, 2, 6 months in 9-14 years old healthy females.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01462357
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 3
Start date November 21, 2011
Completion date October 27, 2015

See also
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