Breakdown | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | |||||
Total Revenue | 846.34M | 345.18M | 1.03B | 4.30B | 18.54M |
Gross Profit | 601.91M | -876.02M | -186.61M | 3.00B | 4.74M |
EBITDA | -134.84M | -1.65B | -1.03B | 1.98B | -402.97M |
Net Income | -378.88M | -1.48B | -964.76M | 1.91B | -358.49M |
Balance Sheet | |||||
Total Assets | 7.96B | 9.32B | 11.47B | 11.87B | 6.75B |
Cash, Cash Equivalents and Short-Term Investments | 3.20B | 4.12B | 5.95B | 7.78B | 5.11B |
Total Debt | 2.01B | 2.70B | 2.70B | 1.37B | 142.54M |
Total Liabilities | 3.05B | 4.03B | 4.22B | 3.33B | 677.22M |
Stockholders Equity | 4.91B | 5.27B | 6.75B | 8.00B | 6.07B |
Cash Flow | |||||
Free Cash Flow | -626.42M | -1.53B | -2.96B | 811.42M | -740.16M |
Operating Cash Flow | -168.79M | -916.25M | -1.89B | 2.01B | -469.39M |
Investing Cash Flow | 3.96M | -449.65M | -1.19B | -2.53B | -182.71M |
Financing Cash Flow | -334.18M | -7.58M | 854.60M | 1.56B | 4.94B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.26 | -41.41% | 2.22% | 22.87% | -2.01% | |
49 Neutral | HK$14.87B | ― | -3.34% | ― | 45.73% | 80.77% | |
― | $5.74B | 9.93 | 7.53% | 7.16% | ― | ― | |
― | $4.79B | 13.62 | 15.72% | 3.94% | ― | ― | |
― | $10.10B | 13.56 | 6.88% | 2.02% | ― | ― | |
― | €3.36B | 9.23 | 5.89% | ― | ― | ― | |
73 Outperform | HK$218.11B | 41.49 | 16.09% | 0.93% | 8.68% | 0.82% |
CanSino Biologics Inc. has received approval from the National Medical Products Administration of China to conduct clinical trials for its Recombinant Trivalent Poliomyelitis Vaccine. This vaccine, which does not contain viral genetic material and is produced without using live viruses, is expected to have strong safety and immunogenicity profiles. The World Health Organization recommends non-infectious polio VLP-based vaccines, like CanSino’s, as a preferred option for future polio prevention, potentially positioning the company as a key player in the post-eradication polio vaccine market.
CanSino Biologics Inc. has received approval from China’s National Medical Products Administration for its 13-valent Pneumococcal Polysaccharide Conjugate Vaccine (PCV13i). This vaccine, which uses advanced technology to enhance immunogenicity and safety, is the first in the company’s pneumococcal vaccine portfolio to gain such approval. The launch of PCV13i is expected to strengthen CanSino’s product portfolio and improve marketing efficiency, aligning with its existing high-end vaccine offerings.
CanSino Biologics Inc. announced the approval of its Phase I clinical trial for an inhaled tuberculosis booster vaccine in Indonesia. This development is significant as it addresses the limitations of the existing Bacillus Calmette-Guerin vaccine by offering a booster that enhances mucosal immunity, potentially improving tuberculosis prevention efforts in high-burden regions.
CanSino Biologics Inc. has announced the agenda for its 2024 Annual General Meeting, scheduled for June 4, 2025, in Tianjin, China. The meeting will cover several key resolutions, including the approval of the 2024 financial reports, profit distribution plans, and reappointment of auditors. Additionally, shareholders will consider granting mandates for share issuance and repurchase, which could impact the company’s capital structure and market operations.