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Upsher-Smith To Present New Research On USL255 (Extended-Release Topiramate) At 2013 American Epilepsy Society Annual Meeting
Date:11/18/2013

MAPLE GROVE, Minn., Nov. 18, 2013 /PRNewswire/ -- Upsher-Smith Laboratories, Inc. (Upsher-Smith), today announced that it will present new research from its epilepsy clinical development program for USL255 (extended-release topiramate) during the American Epilepsy Society's (AES) 67th Annual Meeting in Washington, DC, December 6-10, 2013.  

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Seven presentations will highlight results from the PREVAIL clinical trial, the first of its kind conducted on an extended-release formulation of topiramate.  The global Phase 3 study enrolled more than 200 patients and assessed the efficacy and safety of USL255 as an adjunctive treatment of epilepsy in patients with refractory partial-onset seizures (POS).  In addition, two presentations will feature Phase 1 findings including the pharmacokinetics of USL255 when sprinkled onto food or swallowed intact and the impact of delayed-dose administration of USL255.

USL255 is a once-daily, broad-spectrum antiepileptic drug specifically engineered to deliver a smooth pharmacokinetic profile.  It is being developed by Upsher-Smith for the management of seizure disorders.  Upsher-Smith's New Drug Application for USL255 has been accepted for review by the U.S. Food and Drug Administration (FDA).

"This year's AES meeting marks the first time the findings from our Phase 3 trial will be presented publicly," said William Pullman, MB BS, BMedSc, PhD, FRACP, Chief Scientific Officer, Upsher-Smith.  "We look forward to sharing data from the first global Phase 3 clinical trial of an extended-release formulation of topiramate with the epilepsy community at this year's Annual Meeting." 

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SOURCE Upsher-Smith Laboratories, Inc.
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