pSivida seeks European regulatory nod for Durasert

pSivida (NSDQ:PSDV) is looking to market its Durasert 3-year treatment for posterior segment uveitis in the European Union. Today, the Watertown, Mass.-based company submitted a marketing authorization application to the European Medicines Agency.
Earlier this month, pSivida reported that its 2nd Phase III trial, which followed patients for 3 years, met its primary endpoint of prevention of recurrence of posterior uveitis at 6 months.
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Source: Mass Device - June 22, 2017 Category: Medical Devices Authors: Sarah Faulkner Tags: Drug-Device Combinations Implants Optical/Ophthalmic Pharmaceuticals Regulatory/Compliance Wall Street Beat pSivida Corp. Source Type: news