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LEPU BIO-B
02157.HK
Lepu Biopharma Co., Ltd., a biopharmaceutical company, focuses on the discovery, development, and commercialization of first-in class and best-in-class drug candidates in anti-tumor targeted therapy and oncology immunotherapy in China and internationally. The company offers PUYOUHENG (Pucotenlimab Injection), a humanized IgG4 mAb against human PD-1 for the treatment of solid tumors and melanoma. It is also developing MRG003 that is in phase III clinical study for treating nasopharyngeal cancer, and head and neck squamous cell carcinoma; and MRG002, which is in phase III trials to treat breast and urothelial cancer, as well as HER2-positive. In addition, the company is developing MRG001 CD20-targeted ADC for treating non-Hodgkin’s lymphoma; CMG901 CLDN18.2-targeted ADC for treating gastric and gastroesophageal junction carcinoma and other solid tumors; and MRG004A TF-targeted ADC for treating advanced or metastatic solid tumors.
1.305 T
02157.HKMarket value -Rank by Market Cap -/-

Financial Score

21/12/2025 Update
C
BiotechnologyIndustry
Industry Ranking21/52
Industry medianC
Industry averageC
Score Analysis
Peer Comparison
  • Criteria
    Rating
  • Profit ScoreD
    • ROE-21.35%E
    • Profit Margin-25.30%E
    • Gross Margin94.12%A
  • Growth ScoreB
    • Revenue YoY242.06%A
    • Net Profit YoY-144.37%E
    • Total Assets YoY-1.45%D
    • Net Assets YoY-19.62%E
  • Cash ScoreC
    • Cash Flow Margin-395.29%D
    • OCF YoY242.06%A
  • Operating ScoreD
    • Turnover0.29D
  • Debt ScoreD
    • Gearing Ratio69.86%D

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    News
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    Understanding the Market | LEPU BIO-B rose over 4% in early trading as MRG003 is expected to be included in breakthrough therapy designation targeting refractory nasopharyngeal carcinoma

    LEPU BIO-B rose over 4% in early trading, as of the time of writing, it increased by 4.11%, priced at HKD 7.34, with a transaction volume of HKD 30.16 million. In terms of news, on September 19, the CDE official website announced that LEPU BIO's EGFR-targeted ADC drug MRG003 is proposed to be included in the breakthrough therapy designation, indicated for use in combination with Pembrilizumab (PD-1 monoclonal antibody) for the treatment of recurrent or metastatic nasopharyngeal carcinoma in patients who have previously failed platinum-based and PD-1/PD-L1 inhibitor treatments. It is reported that MRG003 is currently the leading EGFR ADC drug in global development progress, having previously received breakthrough therapy designation and priority review qualification from the CDE, as well as orphan drug status, fast track designation, and breakthrough therapy designation from the FDA. In September 2024, LEPU BIO initially submitted a marketing application for this drug for nasopharyngeal carcinoma, but later withdrew it voluntarily due to the need for supplementary materials, and resubmitted it in March this year. It is currently included in the priority review process for monotherapy in specific recurrent/metastatic nasopharyngeal carcinoma patients

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