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Published 19 November 2008, doi:10.1136/bmj.a2554
Cite this as: BMJ 2008;337:a2554
| The first 150 words of the full text of this article appear below. |
The government chose the human papillomavirus (HPV) vaccine of GlaxoSmithKline (GSK), Cervarix, after considering protection against cancer causing HPV 16 and 18, HPV 6 and 11 (which cause genital warts), and HPV strains not included in the vaccine formulation; price; and supply.1
Its decision was based on a comprehensive review of published and unpublished clinical efficacy and safety data. New data from GSK included the demonstration of high protection against HPV 16 and 18 for over 6.4 years, the longest protection reported for any cervical cancer vaccine to date. The study is being extended for up to 9.5 years in a subset of women.
The UK has awarded a national licence, but in many other European countries licences are awarded regionally. Only once licensed in a country can a vaccine compete in tender applications. Gardasil was licensed in the European Union a year before Cervarix, and was, until recently, the
Pim Kon, medical director1
1 GlaxoSmithKline UK, Uxbridge UB11 1BT
pim.7.kon@gsk.com