Breakdown | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | |||||
Total Revenue | 5.28B | 5.45B | 7.16B | 6.37B | 5.33B |
Gross Profit | 1.76B | 1.80B | 2.33B | 2.03B | 2.09B |
EBITDA | 1.20B | ― | 1.37B | 726.64M | 1.88B |
Net Income | 646.74M | ― | 727.43M | 240.79M | 1.02B |
Balance Sheet | |||||
Total Assets | 17.34B | 19.20B | 20.81B | 19.11B | 19.03B |
Cash, Cash Equivalents and Short-Term Investments | 2.56B | 2.27B | 3.45B | 3.93B | 3.54B |
Total Debt | 2.98B | 3.78B | 6.46B | 5.65B | 5.65B |
Total Liabilities | 5.14B | 7.22B | 8.41B | 7.58B | 7.34B |
Stockholders Equity | 12.15B | 11.91B | 12.31B | 11.41B | 11.57B |
Cash Flow | |||||
Free Cash Flow | 1.99B | ― | ― | ― | ― |
Operating Cash Flow | 2.19B | 398.22M | ― | ― | 37.28M |
Investing Cash Flow | ― | 1.22B | 249.84M | 719.93M | ― |
Financing Cash Flow | ― | ― | 329.56M | ― | 2.51B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
68 Neutral | HK$20.40B | 13.92 | 5.33% | 0.89% | -5.05% | ― | |
52 Neutral | $7.60B | 0.11 | -62.95% | 2.07% | 16.16% | 0.31% | |
― | £2.32B | 75.88 | 5.02% | ― | ― | ― | |
― | $9.22B | 13.39 | 6.22% | 1.16% | ― | ― | |
― | €3.85B | 8.54 | 4.91% | ― | ― | ||
65 Neutral | HK$14.96B | 28.61 | 5.88% | ― | -42.02% | -76.29% | |
47 Neutral | HK$12.99B | ― | -4.41% | ― | 94.98% | 85.69% |
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. has announced the schedule for its 2024 Annual General Meeting (AGM), set to take place on May 22, 2025, in Shenzhen, China. The AGM will address several key resolutions, including the approval of the 2024 Work Reports, Annual Report, Profit Distribution Proposal, and amendments to the Share Incentive Schemes. Additionally, special resolutions will cover the re-appointment of auditors, purchase of wealth management products, and application for credit lines. These resolutions are crucial for the company’s strategic planning and financial management, potentially impacting its operational efficiency and stakeholder relations.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. has released its unaudited first quarterly report for 2025, covering the period ending March 31, 2025. The report, prepared according to PRC Accounting Standards, was approved by the board of directors, with all directors in attendance. The company emphasizes the accuracy and completeness of the report, reflecting its commitment to transparency and accountability in its financial disclosures.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. announced that its enoxaparin sodium injection, Ivenoxin, has received approval from the South African Health Products Regulatory Authority for sale in South Africa. This approval enhances the company’s global market share and demonstrates its capability to penetrate overseas markets. The company plans to continue its international expansion and strengthen its sales channels worldwide.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. announced that its board of directors will meet on April 24, 2025, to review and approve the company’s first-quarter results for the period ending March 31, 2025. This meeting is significant as it will provide insights into the company’s financial performance, potentially impacting its market positioning and stakeholder interests.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. announced a change in the composition of its Nomination Committee, effective March 31, 2025. Mr. Li Li, the chairman of the board, has stepped down from the committee, while Ms. Li Tan, an executive director and deputy general manager, has been appointed as a new member. This change may impact the company’s governance structure and strategic decision-making processes.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. has announced the composition of its board of directors and their respective roles within the company. This announcement includes the appointment of executive and independent non-executive directors, as well as the allocation of roles within the company’s four board committees, which are crucial for strategic decision-making and governance.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. has announced a final cash dividend of RMB 2.5 per 10 shares for the financial year ending December 31, 2024. The dividend will be paid on July 22, 2025, following shareholder approval on May 22, 2025. This announcement reflects the company’s financial performance and commitment to returning value to its shareholders, potentially impacting its market position positively.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. reported its consolidated annual results for the year ending December 31, 2024, showing a slight decrease in revenue to RMB5,258.9 million compared to the previous year. However, the company achieved a significant increase in gross profit to RMB1,739.3 million, with a gross profit margin of 33.1%. The company also reported a profit attributable to equity holders of RMB646.7 million, a notable recovery from the previous year’s loss. The Board has proposed a final cash dividend, reflecting a positive outlook for stakeholders.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. has announced that its board of directors will convene on March 28, 2025, to approve the annual results for the year ending December 31, 2024, and to consider recommending a final dividend. This meeting is significant as it will determine the company’s financial performance for the past year and potentially impact shareholder returns through dividend announcements.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. announced that its enoxaparin sodium injection, Enoparin, has received approval from Argentina’s National Administration of Drugs, Food and Medical Devices for market sales. This approval is expected to enhance the company’s global market share and demonstrates its capability to penetrate international markets, supporting its strategy to expand its global footprint and strengthen its sales channels.
Shenzhen Hepalink Pharmaceutical Group has received approval from the National Medical Products Administration for a clinical trial of its new drug, H1710, designed to treat advanced solid tumors. H1710 is a novel heparanase inhibitor showing significant anti-tumor effects in preclinical studies, positioning the company at the forefront of developing unique anticancer therapies. However, the approval for clinical trials marks just the beginning, as there are inherent risks and uncertainties involved in the drug development process.
Shenzhen Hepalink Pharmaceutical Group Co., Ltd. has obtained a GMP certificate for its new pre-filled formulation production lines from the European Medicines Agency, indicating compliance with EU standards. This certification is expected to enhance the company’s market competitiveness in Europe, where it already holds a strong position in the Enoxaparin Sodium formulations market, and support its internationalization strategy.