Beijing Centergate Technologies (Holding) Co., Ltd. (000931.SZ) has announced that its subsidiary, Duoduo Pharmaceutical Co., Ltd., recently received the "Acceptance Notice" issued by the National Medical Products Administration (NMPA). The marketing authorization application for ticagrelor tablets (specifications: 60mg and 90mg) has been formally accepted.
Ticagrelor tablets are intended for use in combination with aspirin in patients with acute coronary syndrome (ACS) or those with a history of myocardial infarction and at least one high-risk factor for atherothrombotic events (as referenced in the PEGASUS clinical trial). The therapy aims to reduce the incidence of cardiovascular death, myocardial infarction, and stroke.
This regulatory milestone marks a significant step forward in the company's pharmaceutical pipeline, reinforcing its commitment to expanding therapeutic options for patients with serious cardiovascular conditions.