SSY GROUP (02005.HK): Choline Fenofibrate Sustained-release Capsule Obtains Drug Production Registration Approval

NewTimeSpace News: SSY GROUP (02005.HK) announced that the Group has obtained the drug production registration approval issued by NMPA for Choline Fenofibrate Sustained-release Capsule (135mg). Classified as Category 4 chemical drug, it is deemed to have passed consistency evaluation. The product is mainly applied to reduce triglyceride levels in patients with severe hypertriglyceridemia and treat primary hypercholesterolemia.

NewTimeSpace News: SSY Group (02005.HK) released a voluntary announcement on 16 July 2026. The Group has secured the drug production registration approval from the National Medical Products Administration (NMPA) for Choline Fenofibrate Sustained-release Capsule (135mg). As a Category 4 chemical drug, it is deemed to have passed generic consistency evaluation.

On the basis of dietary control for adult patients, the product is indicated for lowering triglyceride levels in patients with severe hypertriglyceridemia, as well as treating patients with primary hypercholesterolemia or mixed dyslipidaemia.

Compared with conventional fenofibrate, choline fenofibrate delivers direct therapeutic effect with less liver and kidney burden. Its administration is not affected by food intake and can be safely combined with statins. It serves as an upgraded high-end triglyceride-lowering product with strong clinical demand.

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