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Imprimis Announces Successful Results from its Pharmacokinetic Study for its Impracor Topical NSAID
Date:2/19/2013

h the FDA has mandated as a part of the clinical development of our Impracor topical NSAID program.  This study provides us with greater confidence in the performance of Impracor as we ready our team for our Phase 3 human clinical trials which are being planned to start in a matter of months."  

"We are happy with the successful outcome of this FDA recommended pharmacokinetic study comparing blood levels of ketoprofen under different 'real world' conditions," said Dr. Joachim Schupp , Imprimis Chief Medical Officer. "The results are consistent with previous pharmacokinetic findings with Impracor and provide guidance for safe dosing in our upcoming efficacy trials," Dr. Schupp added.

The study was conducted by Novum Pharmaceutical Research Services, based in Pittsburgh, PA, at the in-house clinical research facility in Las Vegas, NV. PPD Laboratories in Middleton, WI performed the analysis of the active drug in the blood samples.

About Imprimis Pharmaceuticals, Inc.

Imprimis Pharmaceuticals is a specialty pharmaceutical company focused on the commercial development of compounded drug formulations.  Through an exclusive strategic relationship with the largest compounding pharmacy organization in North America, Imprimis expects to use its proprietary Accudel drug delivery technology, coupled with licensed technologies, and proprietary formulations and market data, to identify pharmaceutical development opportunities where there is a significant unmet need for a new drug product.  Imprimis is also internally developing non-invasive, topically delivered products. Our innovative patented Accudel cream formulation technology is designed to enable highly targeted site-specific treatment. Impracor, our lead Phase 3 pain product candidate, utilizes the Accudel platform technology to d
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SOURCE Imprimis Pharmaceuticals, Inc.
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