| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 543.72M | 417.31M | 246.37M | 158.96M | 56.15M | 13.10M |
| Gross Profit | 231.51M | 225.06M | 144.37M | 102.92M | 36.94M | 11.37M |
| EBITDA | -198.88M | -188.03M | -320.62M | -359.98M | -249.81M | -2.26B |
| Net Income | -249.25M | -268.27M | -379.79M | -402.64M | -259.99M | -2.26B |
Balance Sheet | ||||||
| Total Assets | 3.90B | 3.97B | 3.27B | 3.04B | 3.33B | 2.60B |
| Cash, Cash Equivalents and Short-Term Investments | 578.27M | 769.21M | 1.05B | 1.29B | 1.77B | 2.03B |
| Total Debt | 83.22M | 25.78M | 137.98M | 29.58M | 11.21M | 7.24M |
| Total Liabilities | 243.82M | 200.19M | 351.03M | 295.04M | 222.88M | 97.23M |
| Stockholders Equity | 3.65B | 3.77B | 2.92B | 2.75B | 3.11B | 2.50B |
Cash Flow | ||||||
| Free Cash Flow | -195.07M | -408.97M | -539.79M | -510.66M | -861.66M | -517.18M |
| Operating Cash Flow | -160.92M | -178.83M | -177.93M | -200.66M | -196.85M | -212.57M |
| Investing Cash Flow | -174.67M | 275.91M | -259.78M | 229.15M | -1.35B | 629.70M |
| Financing Cash Flow | -69.99M | -213.79M | 108.66M | -9.22M | 668.85M | 1.53B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
55 Neutral | HK$8.46B | -30.34 | -7.26% | ― | 2.10% | -1350.00% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | HK$6.92B | -23.58 | -7.71% | ― | 74.73% | 32.13% | |
47 Neutral | HK$1.72B | -5.70 | -14.84% | ― | -38.38% | -22.12% | |
42 Neutral | HK$8.81B | -19.44 | -95.84% | ― | -55.64% | -158.67% | |
40 Underperform | HK$10.71B | -51.15 | -21.42% | ― | 240.05% | -140.09% |
Ocumension Therapeutics announced that its biosimilar product OT-702, developed in collaboration with Shandong Boan Biotechnology, has received marketing approval from China’s National Medical Products Administration for treating neovascular age-related macular degeneration and diabetic macular edema. This approval positions Ocumension to potentially expand its market presence in China, leveraging its exclusive rights to promote and commercialize OT-702, which is similar to the globally approved EYLEA. The approval allows the company to apply for additional indications, potentially broadening its therapeutic offerings in the Chinese market.