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Business North Carolina • March, 2008 • Triangle
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CHAPEL HILL -- Pozen expects to hear by mid-April whether its migraine treatment will be approved by the federal Food and Drug Administration. In August, the agency requested further study of whether Treximet, formerly known as Trexima, could cause genetic damage. Pozen submitted the latest study to the FDA in March. Treximet would be its first product.


COPYRIGHT 2008 Business North Carolina Reproduced with permission of the copyright holder. Further reproduction or distribution is prohibited without permission.
Copyright 2008 Gale, Cengage Learning. All rights reserved. Gale Group is a Thomson Corporation Company.
NOTE: All illustrations and photos have been removed from this article.


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