BRIEF— Mochida files NDA for Epadel in China
Japan’s Mochida Pharmaceutical announced that it has submitted a New Drug Application (NDA) to the China National Medical Products Administration (NMPA) for Epadel S (MND-21), a highly purified eicosapentaenoic acid (EPA) ethyl ester formulation that is being jointly developed in China by Mochida and Sumitomo Pharma (Suzhou) Co, a Chinese subsidiary of Sumitomo Pharma Co.
As the clinical Phase III trial conducted in patients with severe hypertriglyceridemia in China has shown positive results, Mochida has submitted a New Drug Application for Epadel S.
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