January 21, 2013

FDA approves alternative storage conditions for EGRIFTATM

Theratechnologies Inc. (TSX: TH) (NASDAQ: THER) announced today that the U.S. Food and Drug Administration (FDA) has granted approval of a Supplemental New Drug Application (sNDA), filed by its commercial partner, EMD Serono, Inc., providing for the revision of the EGRIFTATM (tesamorelin for injection) prescribing information, to include storage conditions for the 2 mg vial up to 12 weeks at or below 25°C after dispensing to the patient.