Alphamab Oncology

HKSE 9966.HK

Alphamab Oncology EBITDA Margin for the year ending December 31, 2023: -59.10%

Alphamab Oncology EBITDA Margin is -59.10% for the year ending December 31, 2023, a 74.83% change year over year. EBITDA Ratio is the proportion of Earnings Before Interest, Taxes, Depreciation, and Amortization to total revenue, assessing a company's operational profitability before non-operating expenses and non-cash charges.
  • Alphamab Oncology EBITDA Margin for the year ending December 31, 2022 was -234.85%, a 4.25% change year over year.
  • Alphamab Oncology EBITDA Margin for the year ending December 31, 2021 was -245.26%.
  • Alphamab Oncology EBITDA Margin for the year ending December 31, 2019 was -5,560.30%.
Key data
Date EBITDA Margin EBIT Margin Depreciation and Amortization EBIT
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SV Wall Street
HKSE: 9966.HK

Alphamab Oncology

CEO Dr. Ting Xu Ph.D.
IPO Date Dec. 12, 2019
Location China
Headquarters No. 175 Fangzhou Road
Employees 429
Sector Healthcare
Industries
Description

Alphamab Oncology, a clinical stage biopharmaceutical company, engages in the discovery, development, manufacture, and commercialization of oncology biologics. Its product pipeline includes KN046, a bispecific monoclonal antibody (BsAb) immune checkpoint inhibitor, which is in pivotal Phase III clinical trials that targets clinically-validated immune checkpoints, including programmed death ligand 1 (PD-L1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4); and KN026, a next generation anti-human epidermal growth factor receptor 2 (HER2) BsAb that is in Phase II clinical trials for treating HER2-positive breast cancers and I/II clinical trial treatment of heavily pre-treated breast cancers, as well as Phase II clinical trial for HER2-positive solid tumors. The company's product pipeline also comprises KN019, a CTLA-4-based immunosuppressant fusion protein, which is in Phase II clinical trial with potential broad applications in both auto-immune diseases and oncology treatment-induced immune disorders; and KN035, an injectable PD-L1 inhibitor that has completed phase II pivotal clinical trials for deficient mismatch repair/microsatellite instability-high solid tumors, and is in Phase III pivotal trials for biliary tract cancer. In addition, its product pipeline also includes KN052 an innovative PD-L1/OX40 bispecific antibody, which is in phase Ia/Ib clinical trial for the treatment of advanced solid tumors. The company was founded in 2008 and is headquartered in Suzhou, the People's Republic of China.

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StockViz Staff

February 8, 2025

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