<< Siemens recognized as one of the top 100 employers in Canada | Biocare Medical on the 2009 Inc. 5000 list of the fastest-growing private companies in the nation >>
Read in | English | Español | Français | Deutsch | Português | Italiano | 日本語 | 한국어 | 简体中文 | 繁體中文 | Русский

Advisory Committee on Immunization Practices supports the permissive use of GARDASIL

Published on October 22, 2009 at 5:17 AM · No Comments

Merck & Co., Inc. announced today that the U.S. Centers for Disease Control and Prevention’s (CDC’s) Advisory Committee on Immunization Practices (ACIP) supports the permissive use of GARDASIL® [Human Papillomavirus Quadrivalent (Types 6, 11, 16 and 18) Vaccine, Recombinant] for boys and young men ages 9 to 26, which means that GARDASIL may be given to males ages 9 to 26 to reduce the likelihood of acquiring genital warts at the discretion of the patient's health care provider. The ACIP also voted to recommend that funding be provided for the use of GARDASIL in males through the Vaccines for Children (VFC) program.

On October 16, the Food and Drug Administration (FDA) approved GARDASIL for use in boys and men 9 through 26 years of age for the prevention of genital warts caused by HPV types 6 and 11, making GARDASIL the only HPV vaccine approved for use in males. GARDASIL is also the only HPV vaccine that protects against HPV types 6 and 11 which cause approximately 90 percent of all genital warts cases.

“We are pleased that the ACIP has provided VFC funding for the use of GARDASIL in males, which should enable access to this important public health advance,” said Mark Feinberg M.D., Ph.D., vice president of Policy, Public Health and Medical Affairs, Merck Vaccines and Infectious Diseases. “We remain committed to helping to prevent HPV-related diseases in both males and females.”

For females, the ACIP also voted to recommend vaccination with either the bivalent or the quadrivalent HPV vaccine for the prevention of HPV 16 and -18 related cervical cancers, precancers and dysplastic lesions, and recommended vaccination with the quadrivalent HPV vaccine, GARDASIL, for the prevention of cervical, vulvar and vaginal cancers, precancers and dysplastic lesions due to HPV types 16 or 18, and for prevention of genital warts due to HPV types 6 or 11.

GARDASIL is approved in the U.S. for use in girls and young women 9 through 26 years of age 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. It is estimated that HPV types 16 and 18 account for 70 percent of cervical and vaginal cancer cases and up to 50 percent of vulvar cancer cases. Types 6 and 11 cause approximately 90 percent of all genital warts cases.

Approximately 75 to 80 percent of people acquire one or more types of HPV at some point in their lives. Nearly 17,000 new cases of genital HPV infection, of any type, occur each day in the U.S., in both males and females. For most people, the virus will go away on its own. But, for some people who don't clear certain types of the virus, HPV diseases can develop, and there is no way to predict who will or won't clear the virus. It is estimated that one million people in the U.S. will develop genital warts. Some resolve without treatment; but, for those that require treatment, warts recur in at least 25 percent of cases.

CDC adds GARDASIL to Vaccines for Children (VFC) program

Comments
The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News-Medical.Net.



  Country flag

biuquote
  • Comment
  • Preview
Loading