- Business
- Jiangsu Sinopep-Allsino Biopharmaceutical Co., Ltd. (688076.SS) is a leading China-based biomedical company that specializes in the research, development, production, sale, and technical services of peptide drugs, oligonucleotides, and small molecule drugs. The company operates through customized product and independently selected product businesses; its customized segment provides CDMO (Contract Development and Manufacturing Organization) services, CRO (Contract Research Organization) technical services, and technology transfer for peptides, oligonucleotides, small molecules, and conjugates including peptide-oligonucleotide conjugates (POCs), peptide-conjugated PMOs (PPMOs), and peptide-drug conjugates (PDCs); it also offers generic APIs such as semaglutide, liraglutide, oseltamivir phosphate, thymalfasin, eptifibatide, bivalirudin, octreotide acetate, lanreotide acetate, cetrorelix, fulvestrant, and inclisiran, alongside intermediate products and finished dosage form (FDF) formulation services for oral solid dosage forms and lyophilized powder injections. Founded in 2009, the company is headquartered in Hangzhou, Zhejiang Province, China, with key manufacturing sites in Lianyungang (Jiangsu), Jiande, Hainan, and Hangzhou (including the Xiasha site via subsidiary Apextide); it serves pharmaceutical and biotechnology clients in domestic China and overseas markets, targeting high-demand therapeutic areas such as diabetes, cardiovascular diseases, oncology, antiviral treatments, and assisted fertility. Recent developments include the establishment of a strategic joint venture with Vazyme (688105.SH) in 2025 to advance synthetic biology applications across biopharmaceuticals, animal healthcare, and agriculture, with Sinopep holding majority control; the launch of its fourth-generation large-scale peptide production facility (Workshop 601) at Lianyungang; FDA acceptance of a DMF for inclisiran API by subsidiary Apextide in April 2025 and successful completion of an FDA GMP inspection at Apextide; receipt of the first FDA Adequate Letter for semaglutide in 2024; achievement of Brazilian ANVISA GMP certification for the Lianyungang facility; a strategic cooperation agreement with Spraying Systems Co.; and EcoVadis sustainability certifications, including a Silver Rating for the ApexTide Hangzhou site and Bronze Medals for Jiande and Lianyungang sites.