Veloxis Pharmaceuticals A/S Announces Financial Results for the First Three Months of 2013

Published: May 16, 2013

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HORSHOLM, Denmark, May 15, 2013 /PRNewswire/ --


•On 29 April, 2013 Veloxis submitted the MAA to the European Medicines Agency (EMA) seeking approval to market LCP-Tacro™ for the prevention of organ rejection in kidney transplant patients in the European Union. The MAA submission is based on the favorable results of the LCP-Tacro™ Phase III 3001 study in stable kidney transplant patients and data from an extensive Phase I and II clinical program. Veloxis expects the decision from the European Union in 2014.

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