EMEA committee recommends approval of Gilead's Viread

18 October 2001

The European Commission's Committee for Proprietary Medicinal Productshas recommended granting marketing authorization for Gilead Sciences' HIV treatment Viread (tenofovir disoproxil fumarate), to be taken in combination with other antiretroviral agents. The company is expecting European authorization early next year.

The US Food and Drug Administration's Antiviral Drugs Advisory Committee also recommended marketing approval of Viread earlier this month.

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