- Hengrui said its subsidiary Fujian Shengdi received regulatory clearance in China to begin clinical trials of HRS9531, targeting risk reduction of major cardiovascular events in patients with atherosclerotic cardiovascular disease.
- The company stated there are no approved comparable drugs globally for this indication, positioning the program in a less crowded competitive landscape.
- Hengrui reported cumulative R&D spending for the HRS9531 program of about CNY 631.5 million.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Jiangsu Hengrui Medicine Co. Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260326-12069002), on March 26, 2026, and is solely responsible for the information contained therein.
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