| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 84.35M | 91.95M | 67.31M | 160.13M | 28.77M | 0.00 |
| Gross Profit | 65.15M | 74.17M | 55.01M | 132.00M | 24.19M | 0.00 |
| EBITDA | -268.37M | -348.82M | -550.31M | -866.06M | -614.32M | -501.94M |
| Net Income | -228.59M | -319.25M | -581.18M | -601.49M | -655.53M | -2.93B |
Balance Sheet | ||||||
| Total Assets | 1.27B | 1.34B | 1.62B | 2.14B | 2.56B | 3.19B |
| Cash, Cash Equivalents and Short-Term Investments | 794.19M | 900.24M | 1.19B | 1.79B | 2.37B | 3.11B |
| Total Debt | 234.85M | 249.44M | 201.02M | 57.95M | 14.81M | 10.92M |
| Total Liabilities | 499.29M | 493.93M | 471.20M | 428.84M | 163.29M | 156.59M |
| Stockholders Equity | 766.33M | 850.80M | 1.15B | 1.71B | 2.39B | 3.04B |
Cash Flow | ||||||
| Free Cash Flow | -194.19M | -382.57M | -778.87M | -665.56M | -581.04M | -358.87M |
| Operating Cash Flow | -149.99M | -321.96M | -665.77M | -572.18M | -557.65M | -307.12M |
| Investing Cash Flow | 370.46M | 345.24M | 587.07M | -208.16M | -103.88M | -600.57M |
| Financing Cash Flow | 52.46M | 45.17M | 131.84M | -20.73M | -81.29M | 2.79B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
58 Neutral | HK$1.54B | 188.57 | 0.99% | ― | 9.41% | -32.69% | |
54 Neutral | HK$13.12B | -44.32 | -12.74% | ― | -76.58% | -4.90% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | HK$2.02B | -10.09 | -55.33% | ― | -100.00% | 30.68% | |
41 Neutral | HK$2.52B | -10.52 | -26.73% | ― | 49.64% | 59.58% | |
39 Underperform | HK$2.63B | -3.72 | -129.05% | ― | ― | -18.99% | |
37 Underperform | HK$1.76B | -6.43 | ― | ― | ― | 27.90% |
Antengene Corporation Limited announced that the Hong Kong Department of Health has approved two supplemental New Drug Applications for XPOVIO® (selinexor) for additional indications in multiple myeloma and diffuse large B-cell lymphoma. This approval enhances Antengene’s market presence in Hong Kong and potentially broadens its impact on the treatment landscape for these diseases, reinforcing its position as a key player in the biotech industry.
Antengene Corporation Limited announced that the China National Medical Products Administration has approved the investigational new drug application for a Phase Ib/II study of ATG-022 in combination with KEYTRUDA and chemotherapy. This approval marks a significant step for Antengene in advancing its clinical pipeline and strengthening its position in the biotech industry, potentially offering new treatment options for diseases with unmet medical needs.