CHAPEL HILL, N.C.--(BUSINESS WIRE)--POZEN Inc. (NASDAQ: POZN) announced today that it has submitted the findings from the short-term human volunteer study of the genotoxic potential of Treximet™ (formerly known as Trexima™) to the U.S. Food and Drug Administration (FDA). The results of this study, the design of which was agreed upon with the FDA prior to its conduct, indicate that no chromosomal aberrations were induced in peripheral blood lymphocytes when Treximet was administered to volunteers for seven days. The submission of this study report is in addition to the response made to the FDA in October 2007 which provided clarifying information on the Chinese Hamster Ovary (CHO) assay.
