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Safety, immunogenicity, and efficacy of quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine in women aged 24–45 years: a randomised, double-blind trial

✍ Scribed by Nubia Muñoz; Ricardo Manalastas Jr; Punee Pitisuttithum; Damrong Tresukosol; Joseph Monsonego; Kevin Ault; Christine Clavel; Joaquin Luna; Evan Myers; Sara Hood; Oliver Bautista; Janine Bryan; Frank J Taddeo; Mark T Esser; Scott Vuocolo; Richard M Haupt; Eliav Barr; Alfred Saah


Book ID
117304699
Publisher
The Lancet
Year
2009
Tongue
English
Weight
171 KB
Volume
373
Category
Article
ISSN
0140-6736

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## Abstract The prevalence of HPV infection in Latin America is among the highest in the world. A quadrivalent (types 6/11/16/18) human papillomavirus L1 virus‐like‐particle vaccine has been shown to be 95–100% effective in preventing HPV 6/11/16/18‐related cervical and genital disease in women naï