WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Sept. 22, 2006--GARDASIL(R) (Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant Vaccine), the cervical cancer vaccine from Merck & Co., Inc., has been granted a license by the European Commission. GARDASIL has been approved as the first and only vaccine in the European Union (EU) for use in children and adolescents aged 9 to 15 years and in adult females aged 16 to 26 years for the prevention of cervical cancer, high-grade cervical dysplasias/precancers (cervical intraepithelial neoplasia (CIN 2/3)), high-grade/precancerous vulvar dysplastic lesions (VIN 2/3) and external genital warts (condyloma acuminata) caused by human papillomavirus (HPV) types 6, 11, 16 and 18. This license applies to the 25 countries that are members of the EU, including the five largest which are France, Germany, Italy, Spain and the United Kingdom.
