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海普瑞(09989) - 2023 - 年度业绩
HepalinkHepalink(HK:09989)2024-03-28 14:21

Financial Performance - Revenue for the year ended December 31, 2023, was RMB 5,431.0 million, a decrease of 24.1% compared to RMB 7,151.0 million in 2022[2] - The company's loss attributable to equity holders for 2023 was RMB 783.3 million, compared to a profit of RMB 727.4 million in 2022[2] - The company reported a net loss of RMB 802.2 million for the year, compared to a profit of RMB 715.0 million in 2022[4] - The adjusted profit attributable to equity holders, excluding investment losses and inventory impairment, was RMB 387.0 million, down from RMB 841.9 million in 2022[10] - The total revenue for the year 2023 decreased by 24.1% to RMB 5,430.97 million, compared to RMB 7,151.04 million in 2022[23] - The company reported a pre-tax loss of RMB 928,334,000 for the year, influenced by various expenses including financing costs of RMB 228,087,000[50] Revenue Breakdown - The sales revenue from the formulation business was RMB 2,979.0 million, a decline from RMB 3,210.5 million in 2022[2] - The sales revenue from the API business was RMB 1,307.3 million, down from RMB 2,673.8 million in 2022[2] - The CDMO business generated sales revenue of RMB 967.0 million, compared to RMB 1,084.1 million in 2022[2] - The heparin industry chain business generated sales revenue of RMB 4,286.3 million, compared to RMB 5,884.3 million in 2022[12] - The formulation sales maintained stability with revenue of RMB 2,979.0 million, accounting for 54.9% of total revenue, and a gross profit margin increase to 43.1% from 35.3% in 2022[12] - Revenue from the pharmaceutical segment was RMB 2,979,030,000, while API segment revenue was RMB 1,307,343,000, and CDMO services generated RMB 966,952,000[57] Asset and Liability Management - Total non-current assets as of December 31, 2023, amounted to RMB 8,599.1 million, an increase from RMB 8,343.7 million in 2022[6] - Total current assets decreased to RMB 10,604.3 million from RMB 12,472.3 million in 2022[6] - Total current liabilities were RMB 4,986.2 million, down from RMB 5,575.8 million in 2022[6] - The company's net asset value stood at RMB 11,988,377 thousand, a reduction from RMB 12,409,465 thousand in 2022, reflecting a decline of approximately 3.4%[7] - Total assets were approximately RMB 19,203.4 million, with total liabilities of approximately 7,215.0 million, resulting in a debt-to-asset ratio of about 37.6%[36] Market Conditions and Challenges - In 2023, the global heparin market faced significant challenges, with the average export price of heparin dropping to USD 4,805 per kg by October, down from USD 11,779 per kg in July, marking a decline of about 59%[9] - The overall economic environment in 2023 was characterized by high inflation and tightening monetary policies, with global trade expected to decrease by 5% compared to the previous year[8] - China's GDP growth for 2023 was recorded at 5.2%, with quarterly growth rates of 4.5%, 6.3%, 4.9%, and 5.2% respectively[8] Impairments and Losses - The company recorded an inventory impairment provision of RMB 855.4 million due to the significant drop in heparin prices and demand fluctuations[9] - The company recognized goodwill impairment loss of RMB 68.2 million, primarily due to difficulties in the CDMO asset group and a decrease in innovative drug orders[29] - Impairment loss on property, plant, and equipment, and other intangible assets amounted to RMB 44.5 million, related to the AR-301 injection development project[30] - The total impairment loss recognized in the income statement was RMB 61,067,000, with the highest losses in the API segment[53] Strategic Initiatives and Future Plans - The company aims to expand its heparin product sales scale as a primary task for 2024, focusing on enhancing market share and operational efficiency[22] - The company plans to optimize resource allocation in its CDMO business to meet diverse customer project needs and enhance production capacity[21] - The company is actively expanding its international market presence and enhancing its sales network in the U.S. and Europe to seek new growth opportunities[10] - The company plans to continue exploring collaboration opportunities and accelerate the strategic layout of innovative drugs through partnerships[10] - The company will strengthen its market presence in the U.S. by collaborating with strategic partners and leveraging its own sales team[21] Clinical Trials and Product Development - Oregovomab's Phase III clinical trial did not meet its primary endpoint, but data suggests potential benefits for patients over 65 and those with MRSA, prompting further exploration of a second Phase III study[16] - AR-301's global Phase III study did not achieve its primary endpoint, yet showed promising trends in older patients and those with antibiotic-resistant infections, leading to discussions with FDA and EMA for a new study design[17] - RVX-208 has completed Phase III trials and received breakthrough therapy designation from the FDA, aiming to reduce major adverse cardiovascular events in high-risk patients[18] - H1710, an acetyl heparinase inhibitor, is in preclinical stages and has shown significant anti-tumor effects in various models, with IND applications planned for China and the US[19] Governance and Compliance - The board of directors includes four executive directors and three independent non-executive directors, ensuring that independent opinions are represented[79] - The audit committee has reviewed the consolidated annual performance for the year ending December 31, 2023, and confirmed compliance with relevant accounting standards and regulations[84] - Ernst & Young confirmed that the financial figures in the preliminary announcement align with the consolidated financial statements for the year ending December 31, 2023[85]