7:02AM Aegerion Pharma submits marketing applications for Lomitapide in U.S. and EU (AEGR) 17.10 : Co announced that it has submitted a New Drug Application to the FDA, and a Marketing Authorization Application to the European Medicines Agency seeking approval of Aegerion's lead investigational therapeutic, lomitapide, as an adjunct to a low fat diet and other lipid-lowering therapies to reduce cholesterol in patients with Homozygous Familial Hypercholesterolemia. Co plans to initiate a clinical study of lomitapide for the treatment of FC in 2012.
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