US drug major Merck & Co's cervical cancer vaccine Gardasil has received further approvals from the Food and Drug Administration for the prevention of vulvar and vaginal cancers caused by human papillomavirus types 16 and 18.
The approval, based on data from a combined analysis of more than 15,000 patients, sees Gardasil cleared for the prevention of cervical, vulvar and vaginal cancers caused by HPV types 16 and 18; genital warts caused by HPV types 6 and 11; and precancerous or dysplastic lesions caused by HPV types 6, 11, 16 and 18 in girls and young women aged nine through 26 years.
Label for Gardasil now includes five-year extension study data
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