Studies Demonstrate Gardasil® Has Long Duration of Protection From HPV Disease
LYON, France, December 6, 2012 /PRNewswire/ --
Data represents the largest follow-up available for an HPV vaccine
Data from two large, long term follow-up studies continue to show that vaccination with Gardasil offers a long duration of protection from human papillomavirus (HPV) diseases related to HPV types 6, 11, 16 and 18. HPV-related diseases include cervical cancer and genital warts.
The interim data, presented at the 28th International Papillomavirus Conference (IPV) in Puerto Rico, showed that young women and adolescent girls and boys vaccinated with Gardasil were protected from HPV-related diseases for up to eight years following vaccination. Furthermore, data on immunogenicity (the degree to which an immune response is induced) showed that immune levels remained high for nine years following vaccination.
"These latest data show an encouraging trend of continued protection with Gardasil against HPV-related cervical, vaginal and vulvar disease in women through eight years," said Professor Susanne Krüger Kjær, Danish Cancer Society. "These studies provide further evidence for the ongoing efficacy, immunogenicity, and safety of Gardasil."
The European studies were conducted in Sweden, Denmark, Norway and Iceland. One study followed young women aged between 16-23 years and the second study followed adolescent boys and girls between 9-15 years. The studies will continue tracking the study participants for at least 14 years.
Benoit Soubeyrand, Executive Director, Medical Affairs for Sanofi Pasteur MSD, stated: "These data tell us that Gardasil can in effect help protect people from HPV diseases during the entire period when they are most at risk - from adolescence into early adulthood. That's nearly a decade of protection that could save many lives over time."
More than 100 million doses of Gardasil® have been distributed worldwide since 2006.
Notes to Editors
About the studies
The Scandinavian study among young women is an extension of the pivotal Phase III FUTURE II clinical trial of Gardasil. The study is being conducted through the national health registry systems in four Nordic countries: Denmark, Iceland, Norway and Sweden. Because of the extensive nationwide registers in these countries, it is possible to conduct follow-up studies that can track the health of the study participants well into the future, beyond the original study's timeframe. The Long Term Follow-Up (LTFU) study evaluated effectiveness against the early stages of cervical cancer, vulvar cancer and vaginal cancer related to HPV types 6/11/16/18. Data from this Scandinavian study showed a trend of continued protection, with no breakthrough cases of disease, through eight years. Analysis and observation of the study participants will be followed for 10 years, for a total of 14 years post vaccination.
The study among adolescent girls and boys aged 10-15 years followed a randomized, double-blind trial of 1,781 participants. Safety, immunogenicity and effectiveness of Gardasil were assessed following vaccination in this population as they got older and as some became sexually active. Results also showed persistence of high immune response to HPV types 6, 11, 16 or 18 over 8 years in study participants. In this follow up period there were no cases of disease related to vaccine HPV types 6, 11, 16 or 18 through 8 years. This study will continue to follow participants through at least 10 years of post-vaccination follow-up.
- Krüger Kjær S et al. Long-term effectiveness of Gardasil™ in the Nordic countries. Poster and abstract presented at the 28th International Papillomavirus Conference, Puerto Rico, Nov 30- Dec 6 2012.
- Saah A et al. Long-term extension study of Gardasil in adolescents; results through month 96. Poster and abstract presented at the 28th International Papillomavirus Conference, Puerto Rico, Nov 30- Dec 6 2012.
- Nygård M et al. A long term follow-up study of the immunogenicity of the quadrivalent HPV (qHPV) vaccine in Scandinavia and Iceland. Poster and abstract presented at the 28th International Papillomavirus Conference, Puerto Rico, Nov 30- Dec 6 2012.
About Sanofi Pasteur MSD
Sanofi Pasteur MSD is a joint venture between Sanofi Pasteur, the vaccine division of Sanofi, and Merck, known as MSD outside the USA and Canada. Combining innovation and expertise, Sanofi Pasteur MSD is the only company in Europe dedicated exclusively to vaccines. Sanofi Pasteur MSD is able to draw on the research expertise of Sanofi Pasteur and Merck to focus on the development of new vaccines for Europe to improve the acceptability, efficacy and tolerability of vaccination.
For further information please contact:
Senior Director External Communications Europe
Sanofi Pasteur MSD
Tel : +33-4-37-28-4040
Mob : +33-6-33-46-1365
SOURCE Sanofi Pasteur MSD
More by this Source
GARDASIL® 9: 2-dose Schedule Approved in Europe
07 Apr, 2016, 08:00 BST
Vaxelis®, New Fully-liquid Paediatric Hexavalent Vaccine Approved in the European Union
19 Feb, 2016, 08:00 GMT
Get content for your website
Enhance your website's or blog's content with PR Newswire's customised real-time news feeds.
Contact PR Newswire
Send us an email at MarketingUK@prnewswire.co.uk or call us at +44 (0)20 7454 5382
Become a PR Newswire client
Request more information about PR Newswire products & services or call us at +44 (0)20 7454 5382