Cervarix
The U.S. Food and Drug Administration (FDA) has approved Cervarix [Human papillomavirus bivalent (types 16 and 18) vaccine, recombinant] for the prevention of cervical pre-cancers and cervical cancer associated with oncogenic human papillomavirus (HPV) types 16 and 18 for use in girls and young...
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Cervarix

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Cervarix is Approved in Australia for Females 10-45 Years Old
First major market licence for the GlaxoSmithKline cervical cancer vaccine LONDON UK and RIXENSART Belgium, May 21, 2007 - Cervarix, the cervical cancer vaccine from GSK, has been granted a licence by the Therapeutic Goods Administration (TGA) of Australia for the prevention...
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Cervarix, GSKs Cervical Cancer Vaccine, Wins Tender for Dutch National Immunisation Programme
GlaxoSmithKlines (GSK) cervical cancer vaccine, Cervarix, was today confirmed by the Netherlands Vaccine Institute (NVI) as the cervical cancer vaccine for the Dutch National Immunisation Programme (NIP)....
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Cervarix U.S. Regulatory Update
...-- GlaxoSmithKline today provided the following update regarding its application to the U.S. Food and Drug Administration (FDA) for approval of Cervarix, its vaccine to prevent cervical cancer and cervical pre-cancer related to human papillomavirus types 16 and 18. GSK has submitted final data...
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See also: Human Papillomavirus Prophylaxis

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