- CEO
- Li Li
- Full Time Employees
- 1,926
- Sector
- Healthcare
- Industry
- Drug Manufacturers - Specialty & Generic
- Address
- No. 21 Langshan Road Shenzhen ENG People's Republic of China 518057
- IPO Date
- Apr 13, 2021
- Business
- Shenzhen Hepalink Pharmaceutical Group Co., Ltd. (SHEZF) manufactures and sells pharmaceutical products with a focus on the heparin industrial chain, CDMO services for large molecule biologics, and innovative drug research, development, and commercialization; its core offerings include finished dose products such as enoxaparin sodium injections (branded Inhixa, Neoparin, Prolongin), active pharmaceutical ingredients (APIs) comprising heparin sodium API, enoxaparin sodium API, and pancreatin API, alongside contract development and manufacturing organization (CDMO) services for recombinant biomacromolecules, gene therapy intermediates, and naturally derived pharmaceuticals through subsidiaries Cytovance Biologics and Scientific Protein Laboratories (SPL). Founded in 1998 and headquartered in Shenzhen, China, the company operates globally across over 50 countries and regions, including key markets in Europe, the United States, China, Turkey, Brazil, Thailand, New Zealand, Argentina, and South Africa; it maintains dual listings on the Hong Kong Stock Exchange (9989.HK) and Shenzhen Stock Exchange (002399.SZ), with subsidiaries like Techdow Pharma entities in Europe and the US, Aridis Pharmaceuticals, and OncoVent Biomedical. The company targets healthcare providers, hospitals, and biopharma clients in the anticoagulants, biologics, and oncology sectors, emphasizing vertically integrated heparin production and high-value innovative therapies. Recent developments include receipt of National Medical Products Administration approval in February 2025 for Phase I clinical trials of its in-house heparanase inhibitor H1710 injection for solid tumors, with first patient dosing in July 2025; a distribution agreement with Zhejiang Yongtai Pharmaceutical for US commercialization of Gabapentin capsules; continued advancement of fosaprepitant dimeglumine commercialization in the US via self-operated teams; market authorizations in South Africa, Argentina, Thailand, and New Zealand; European GMP certification and EMA approval for its Pingshan production base, boosting enoxaparin capacity to 550 million doses annually; and a licensing deal for Oregovomab with Orient EuroPharma via subsidiary Shenzhen OncoVent, alongside ongoing Phase III planning for AR-301 (tosatoxumab) targeting ventilator-associated pneumonia. In 2024, the company reported revenue of RMB5.26 billion with gross profit margin rising to 33.1% from 17.3%, driven by double-digit enoxaparin sales growth and CDMO expansion, alongside a shift to profitability with RMB647 million net profit attributable to shareholders; for H1 2025, revenue stood at RMB2.79 billion with enoxaparin sales up 21.6% year-over-year despite API pricing pressures.