Article: Antares Receives First FDA Approval of ATD(TM) Gel Platform.

Approval of Elestrin[TM] Triggers Approximately $2.6 Million Payment

EWING, N.J. -- Antares Pharma, Inc. (Amex: AIS) announced the U.S. Food and Drug Administration (FDA) approved for marketing Elestrin[TM] (formerly Bio-E-Gel[R]) in the United States. Antares' development partner, BioSante Pharmaceuticals (Amex: BPA) announced today that Bio-E-Gel will be marketed under the name Elestrin[TM] by Bradley Pharmaceuticals Inc. (NYSE: BDY) and is indicated for the treatment of moderate-to-severe vasomotor symptoms (hot flashes) associated with menopause. Elestrin is the first FDA approved product in Antares' Advanced Transdermal Delivery (ATD[TM]) gel platform. Two ...

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