NewsInferno
06/17/2010
The Food & Drug Administration (FDA) has put off a decision on whether or not it should approve the expanded use of the Gardasil vaccine to older women, ages 27 to 45. The FDA’s decision, which was expected sometime next week, will not come until later this year.
Approved in 2006, Gardasil prevents four strains of HPV, two of which cause 70 percent of all cervical cancers. The other two HPV strains are responsible for about 90 percent of genital warts. The vaccine is approved for use in girls and young women, ages 9 to 26. Last year, the FDA approved Gardasil’s use in males 9 to 26 years old to prevent genital warts caused by HPV.
Merck has been seeking approval to market Gardasil to older women for more than two years. But according to The Wall Street Journal, the FDA delayed its approval because it wanted longer-term data on Gardasil’s efficacy, after four years of follow-up. Merck & Co., the maker of Gardasil, provided that information last year. The efficacy rate after four years of follow up was 88.7 percent compared with 91 percent after two years.
The FDA would not comment on the delay, the Journal said.
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