Cipher Pharmaceuticals Inc. (TSX: DND) today announced the U.S. Food and Drug Administration ("FDA") has approved CIP-TRAMADOL ER, the Company's extended-release tramadol product, for the treatment of moderate to moderately severe chronic pain in adults.
"This represents our second FDA approval - a major achievement for the Company that reflects a significant amount of effort and dedication from our team, led by Dr. Jason Gross," said Larry Andrews, President and CEO of Cipher. "We are excited about the opportunity for CIP-TRAMADOL ER in the large and growing U.S. pain market. There were more than 28 million tramadol prescriptions written in 2009, only 5% of which were for once-daily formulations, indicating there is a substantial opportunity for a new entrant. We believe our product's unique capsule formulation comprising an immediate-release tablet and sustained-release beads, combined with having no food effect, will make it an attractive alternative for clinicians and chronic pain sufferers."
Cipher is currently preparing for the U.S. commercial launch of the product, which includes securing a marketing partner and finalizing commercial manufacturing requirements. The actual timing of the launch will also be influenced by the outcome of the appeal filed by Purdue Pharma Products L.P. against Par Pharmaceutical, Inc., which relates to the Orange Book-listed patents for Ultram(R) ER, the reference product in Cipher's New Drug Application. A decision in that case is not expected until late 2010.
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