Important note: Information in this article was accurate in 2006. The state of the art may have changed since the publication date.
Important note: Information in this article was accurate in 2006. The state of the art may have changed since the publication date.
Reuters NewMedia - November 9, 2006
The application for the drug ATRIPLA was filed jointly by the three companies through a newly established three-way joint venture based in Ireland, the companies said.
ATRIPLA is a once-daily single tablet regimen approved in the United States for the treatment of HIV-1 infection in adults for use either as stand-alone therapy or in combination with other antiretroviral agents, the companies said.
ATRIPLA was approved by the U.S. Food and Drug Administration on July 12, 2006. In the United States, the product is commercialised by Bristol-Myers Squibb and Gilead Sciences through a joint venture, the companies said.
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