- CEO
- Da Tao Liu
- Full Time Employees
- 1,325
- Sector
- Health technology
- Industry
- Pharmaceuticals: major
- Address
- Building 2 Room 105, No. 230 Cailun RoadChina (Shanghai) Pilot Free Trade Zone Shanghai, 201210China Shanghai SH China 201210
- IPO Date
- Jan 18, 2022
- Business
- Mabwell (Shanghai) Bioscience Co., Ltd. (688062.SS) is a China-based innovation-driven biopharmaceutical company engaged in the research, development, manufacturing, and commercialization of biologic drugs across oncology, immunology, ophthalmology, bone disorders, hematology, infectious diseases, metabolism, and cardiovascular disease; the company offers approved products including JUNMAIKANG (adalimumab biosimilar for autoimmune diseases such as rheumatoid arthritis), MAILISHU and MAIWEIJIAN (denosumab biosimilars for postmenopausal osteoporosis and giant cell tumor of bone), MAILISHENG (albipagrastim alfa, a novel long-acting G-CSF using albumin fusion technology for chemotherapy-induced neutropenia), alongside a robust pipeline of over 30 candidates such as anti-ST2 antibody 9MW1911 (phase II for COPD and fibrosis), anti-IL-11 antibody 9MW3811 (phase II for pathological scarring), B7-H3 ADC 7MW3711 (phase I/II oncology), CDH17 ADC 7MW4911 (IND cleared), anti-VEGF 9MW0813 (NDA submitted for wet AMD), and 9MW3011 (phase II hematology for iron overload). Founded in 2017 and headquartered at Building 3, No. 576 Libing Road, Pudong New Area, Shanghai, China, Mabwell operates manufacturing bases in Taizhou and Shanghai (GMP-compliant, EU QP audited), R&D sites in Shanghai, Beijing, Nanjing, and San Diego, US, and serves domestic and international markets. Recent developments include the September 2025 strategic collaboration with Insilico Medicine and ChemExpress to develop a novel ADC compound library; formation of Kalexo Bio with Aditum Bio for siRNA therapy 2MW7141 in cardiovascular disease; licensing agreements for 9MW3811 with Calico, albipagrastim alfa with Qilu Pharmaceutical, and 9MW3011 with Disc Medicine (up to $412.5 million milestones); NMPA approvals for phase II trials of 9MW3811 and IND clearance for 7MW4911; NDA acceptance for 9MW0813; first-patient dosing in US phase II for 9MW3011; and positive phase IIa data for 9MW1911 reducing severe COPD exacerbations by over 40%.