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Beijing Leadman Biochemistry Co Ltd

Beijing Leadman Biochemistry Co., Ltd. researches, develops, manufactures, and sells in vitro diagnostic reagents and instruments, as well as biochemical raw materials, in the People's Republic of China. Its biochemical raw materials include enzymes, antigens, coenzymes, antibodies, buffers, enzyme substrates, culture mediums, stain agents, amino acids, and other products for biotechnology, clinical diagnosis, drug development, chemical production, and related applications. The company also provides biochemical reagents for liver function, lipid profile, diabetes, pancreas function, tumor detection, protein, and other areas, along with multi calibrators, semi-quantitative assays, coagulation reagents, cardiac markers, electrolytes, and renal function tests; companion reagents for tumor, thyroid hormone, sex hormone, and infectious disease; IDS-compatible luminescent reagents; and testing instruments. Founded in 1997, it is based in Beijing, the People's Republic of China.

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300289.CS

Leadman's 2026 interim report shows net loss of 7.113 million yuan, widening year-on-year

Leadman released its 2026 interim report. Total operating revenue was 152 million yuan, down 5.31% year-on-year. Net loss attributable to the parent company was 7.113 million yuan, a decrease of 2.8679 million yuan compared with the same period last year, with the loss widening year-on-year. Net cash inflow from operating activities was 9.2498 million yuan, up 947.07% year-on-year. The company's asset-liability ratio was 5.24%, gross margin was 43.44%, return on equity was negative 0.44%, and diluted earnings per share was negative 0.01 yuan. The number of shareholders was 25,000, and the top ten shareholders held 50.87% of the total share capital.
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300289.CS

Leadman's first-half loss widens to 7.11 million yuan

Leadman published its 2026 interim report. First-half operating revenue was 152 million yuan, down 5.3 percent year on year, while net profit attributable to the parent swung from a loss of 4.25 million yuan a year earlier to a loss of 7.11 million yuan. Second-quarter operating revenue was 81.5 million yuan, down 0.1 percent year on year, and the net loss attributable to the parent was 3.14 million yuan, wider than the 2.99 million yuan loss in the same period last year. As of the end of the second quarter, total assets were 1.756 billion yuan, down 1.1 percent from the end of the previous year, and net assets attributable to the parent were 1.632 billion yuan, down 0.4 percent. In vitro diagnostic reagents remained the main revenue source, generating 111 million yuan, up 1.69 percent year on year and accounting for 72.85 percent of operating revenue. Diagnostic instruments brought in 17.23 million yuan, down 24.23 percent, representing 11.34 percent of revenue. Biochemical raw materials contributed 6.81 million yuan, down 11.32 percent, or 4.48 percent of revenue. Other businesses generated 17.22 million yuan, down 18.75 percent, or 11.33 percent of revenue. The company's operating model is mainly distribution-based, with distribution revenue of 123 million yuan accounting for 90.98 percent of main business revenue, while direct sales revenue was 12.16 million yuan, or 9.02 percent. The company flagged risks including changes in industry policy and intensifying market competition, and said it has taken measures to address them.
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Biotech & Genomic Medicine2

Leadman Subsidiary's Recombinant Group B Meningococcal Vaccine Receives Clinical Trial Approval

Leadman announced that its subsidiary, Beijing Sinovac Xiangrui Biological Products, has received clinical trial approval from the National Medical Products Administration for its recombinant Group B meningococcal vaccine. The approval allows the company to conduct clinical trials for the prevention of epidemic cerebrospinal meningitis caused by Neisseria meningitidis serogroup B. The vaccine uses a multi-component recombinant protein technology platform and an E. coli expression system. Currently, products from GSK and Pfizer are available globally, and similar domestic projects have also entered the clinical research stage. This approval will not have a significant impact on the company's operating performance for the current year.