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艾美疫苗(06660) - 2025 - 中期业绩
AIM VACCINEAIM VACCINE(HK:06660)2025-08-27 13:43

Financial Highlights This section provides a concise overview of the company's key financial performance indicators for the period | Metric | 2025 (RMB thousands) | 2024 (RMB thousands) | Change (%) | | :--- | :--- | :--- | :--- | | Revenue | 514,657 | 537,178 | -4.2 | | Gross Profit | 341,236 | 388,290 | -12.1 | | Loss Attributable to Owners of the Parent | (131,116) | (139,254) | -5.8 | Interim Condensed Consolidated Statement of Profit or Loss and Other Comprehensive Income This statement presents the company's financial performance, including revenue, expenses, and net loss, for the interim period | Metric | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Revenue | 514,657 | 537,178 | | Cost of Sales | (173,421) | (148,888) | | Gross Profit | 341,236 | 388,290 | | Other Income and Gains | 10,553 | 13,424 | | Selling and Distribution Expenses | (232,057) | (232,240) | | Administrative Expenses | (126,246) | (124,163) | | Research and Development Expenses | (106,962) | (170,110) | | Net Impairment Losses on Financial Assets | (7,644) | (3,857) | | Other Expenses | (2,072) | (656) | | Finance Costs | (28,465) | (29,998) | | Loss Before Tax | (151,657) | (159,310) | | Income Tax Credit | 15,663 | 14,046 | | Loss for the Period | (135,994) | (145,264) | | Loss Attributable to Owners of the Parent | (131,116) | (139,254) | | Loss Attributable to Non-controlling Interests | (6,010) | (4,878) | - Loss for the period narrowed by 6.4% year-on-year to RMB 135,994 thousands67 - Research and development expenses significantly decreased by 37.1% to RMB 106,962 thousands6 Interim Condensed Consolidated Statement of Financial Position This statement outlines the company's assets, liabilities, and equity at a specific point in time, reflecting its financial health | Metric | June 30, 2025 (RMB thousands) | December 31, 2024 (RMB thousands) | | :--- | :--- | :--- | | Total Non-current Assets | 4,973,797 | 4,926,924 | | Total Current Assets | 2,213,931 | 2,387,397 | | Total Current Liabilities | 3,026,219 | 3,090,268 | | Net Current Liabilities | (812,288) | (702,871) | | Total Non-current Liabilities | 617,264 | 612,945 | | Total Equity | 3,544,245 | 3,611,108 | - Net current liabilities expanded to RMB 812,288 thousands, an increase of RMB 109,417 thousands from the end of 20249 - Total non-current assets slightly increased, while total current assets decreased8 Interim Condensed Consolidated Statement of Changes in Equity This statement details the changes in the company's equity components over the interim period, including profit/loss and share issuance | Metric | June 30, 2025 (RMB thousands) | December 31, 2024 (RMB thousands) | | :--- | :--- | :--- | | Equity Attributable to Owners of the Parent | 3,303,535 | 3,365,520 | | Non-controlling Interests | 240,710 | 245,588 | | Total Equity | 3,544,245 | 3,611,108 | - Total equity decreased from RMB 3,611,108 thousands at the end of 2024 to RMB 3,544,245 thousands10 - Loss for the period of RMB 135,994 thousands was partially offset by proceeds from share issuance of RMB 70,062 thousands10 Interim Condensed Consolidated Statement of Cash Flows This statement summarizes the cash inflows and outflows from operating, investing, and financing activities during the interim period | Cash Flow Type | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Net Cash Flows Used in Operating Activities | (96,839) | (97,158) | | Net Cash Flows Used in Investing Activities | (110,808) | (91,532) | | Net Cash Flows From Financing Activities | 2,668 | 130,445 | | Net Decrease in Cash and Cash Equivalents | (204,979) | (58,245) | | Cash and Cash Equivalents at End of Period | 289,507 | 525,343 | - Net cash flows used in operating activities amounted to an outflow of RMB 96,839 thousands, largely consistent with the prior year period13 - Net cash flows used in investing activities increased to an outflow of RMB 110,808 thousands14 - Net cash flows from financing activities shifted from an inflow of RMB 130,445 thousands in the prior year period to an inflow of RMB 2,668 thousands14 Notes to the Interim Condensed Consolidated Financial Information This section provides detailed explanations and additional information supporting the interim condensed consolidated financial statements 1. Company and Group Information Aimei Vaccine Co., Ltd. was incorporated in China in 2011, listed on the HKEX in 2022, focusing on human vaccine R&D, production, and commercialization - The company was incorporated in China on November 9, 2011, and listed on the Main Board of the HKEX on October 6, 20221516 - The Group's principal business involves the research, development, production, and commercialization of human vaccine products in China17 2.1 Basis of Preparation Interim financial information is prepared under IAS 34, should be read with 2024 annual statements, and despite net current liabilities, management deems the going concern assumption appropriate - The financial information is prepared in accordance with IAS 34 and should be read in conjunction with the annual financial statements18 - As of June 30, 2025, the Group's net current liabilities amounted to RMB 812,288 thousands19 - Management has renewed bank borrowings of RMB 128,000 thousands and has unutilized bank facilities of RMB 566,000 thousands, considering the going concern assumption appropriate19 2.2 Changes in Accounting Policies and Disclosures Accounting policies align with 2024 annual statements, with only new IFRS amendments adopted, specifically IAS 21 (lack of exchangeability) having no impact - Accounting policies are consistent with the 2024 annual financial statements, with only the initial adoption of amended IFRS accounting standards20 - The amendments to IAS 21 regarding 'Lack of Exchangeability' had no impact on the Group's interim condensed consolidated financial information22 3. Operating Segment Information The Group's vaccine sales and R&D services are considered a single reportable segment, thus no segment analysis is presented - The Group's business (vaccine sales and R&D services) is considered a single reportable segment23 4. Revenue, Other Income and Gains For the six months ended June 30, 2025, revenue from customer contracts was RMB 514,657 thousands, all from vaccine sales, down 4.2% year-on-year; other income and gains totaled RMB 10,553 thousands, down 21.4%, mainly due to reduced deposit interest income | Metric | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Revenue from Contracts with Customers (Vaccine Sales) | 514,657 | 537,178 | | Total Other Income and Gains | 10,553 | 13,424 | - Vaccine sales revenue decreased by 4.2% year-on-year2425 - Other income and gains decreased by 21.4%, primarily due to reduced deposit interest income2699 5. Finance Costs For the six months ended June 30, 2025, total finance costs were RMB 28,465 thousands, down 5.1% year-on-year, mainly due to reduced bank loan interest expenses | Metric | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Interest on Bank Loans | 37,874 | 40,700 | | Interest on Lease Liabilities | 399 | 988 | | Less: Interest Capitalized | (9,808) | (11,690) | | Total Finance Costs | 28,465 | 29,998 | - Finance costs decreased by 5.1% year-on-year, primarily due to reduced interest expenses on bank loans27105 6. Loss Before Tax For the six months ended June 30, 2025, loss before tax narrowed to RMB 151,657 thousands from RMB 159,310 thousands, influenced by increased inventory write-downs and reduced interest income | Impact Factor | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Cost of Inventories Sold | 173,421 | 148,888 | | Net Exchange Differences | (625) | 154 | | Impairment Provision for Trade and Bills Receivables | 7,644 | 3,857 | | Write-down of Inventories to Net Realizable Value | 40,433 | 3,063 | | Loss on Disposal of Property, Plant and Equipment | 160 | 47 | | Interest Income | (2,314) | (4,356) | - Write-down of inventories to net realizable value significantly increased to RMB 40,433 thousands (2024: RMB 3,063 thousands)28 7. Income Tax Credit For the six months ended June 30, 2025, the company received an income tax credit of RMB 15,663 thousands, up 11.4% year-on-year, mainly due to certain subsidiaries enjoying a 15% high-tech enterprise preferential tax rate | Metric | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Current Income Tax | 4,719 | 6,586 | | Deferred | (20,382) | (20,632) | | Tax Credit for the Period | (15,663) | (14,046) | - Several subsidiaries, including Aimei Action, Aimei Chengxin, Aimei Rongyu, Aimei Jianchi, Aimei Tanxuezhe, and Zhuhai Lifanda, enjoy a 15% preferential corporate income tax rate293031 - Income tax credit increased by 11.4%, primarily due to an increase in loss before tax for a subsidiary106 8. Dividends The Board did not recommend payment of any dividends for the six months ended June 30, 2025, consistent with the prior year period - For the six months ended June 30, 2025, the Board did not recommend the payment of any dividends (2024: nil)33 9. Loss Per Share Attributable to Owners of the Parent For the six months ended June 30, 2025, both basic and diluted loss per share attributable to owners of the parent were RMB 0.11, consistent with the prior year period | Metric | 2025 (RMB) | 2024 (RMB) | | :--- | :--- | :--- | | Basic Loss Per Share | (0.11) | (0.11) | | Diluted Loss Per Share | (0.11) | (0.11) | - The weighted average number of ordinary shares outstanding used to calculate basic and diluted loss per share increased from 1,211,062,599 in 2024 to 1,221,081,936 in 20253436 - Diluted loss per share is equal to basic loss per share as there were no potential ordinary shares outstanding during the period36 10. Property, Plant and Equipment As of June 30, 2025, the Group's property, plant, and equipment had a net book value of approximately RMB 3,276,507 thousands, with some buildings mortgaged for bank loans and others lacking ownership certificates; asset acquisition costs for the period were RMB 55,276 thousands - As of June 30, 2025, buildings with a net book value of approximately RMB 240,724 thousands were pledged as collateral for bank borrowings37 - As of June 30, 2025, buildings with a total net book value of approximately RMB 283,288 thousands had not yet obtained property ownership certificates37 - The cost of assets acquired during the period was RMB 55,276 thousands, a year-on-year decrease of 16.5%37 11. Trade and Bills Receivables As of June 30, 2025, total trade and bills receivables were RMB 1,164,972 thousands, up 3.7% from year-end 2024, mainly due to lower collections in H1; trade receivables have a credit period of two to six months, with strict control over overdue balances | Metric | June 30, 2025 (RMB thousands) | December 31, 2024 (RMB thousands) | | :--- | :--- | :--- | | Trade Receivables | 1,223,370 | 1,173,906 | | Bills Receivables | 399 | 1,000 | | Impairment | (58,797) | (51,153) | | Total | 1,164,972 | 1,123,753 | - Trade and bills receivables increased by 3.7%, primarily due to lower collections in the first half compared to the second half38111 - Trade receivables typically have a credit period of two to six months, and the Group maintains strict control over credit risk38 12. Trade and Bills Payables As of June 30, 2025, total trade and bills payables were RMB 94,264 thousands, a significant 85.2% increase from year-end 2024, driven by trade payables and new bills payables; trade payables are typically settled within 30 to 90 days | Metric | June 30, 2025 (RMB thousands) | December 31, 2024 (RMB thousands) | | :--- | :--- | :--- | | Trade Payables | 64,264 | 50,894 | | Bills Payables | 30,000 | – | | Total | 94,264 | 50,894 | - Trade and bills payables significantly increased by 85.2%, including new bills payables of RMB 30,000 thousands41 - Trade payables are non-interest-bearing and typically settled within 30 to 90 days41 Management Discussion and Analysis This section provides management's perspective on the company's financial performance, operational results, and future outlook Business Overview and Outlook Aimei Vaccine is a leading Chinese vaccine company with a full R&D to commercialization value chain, five technology platforms, and four licensed manufacturers, commercializing 8 vaccines, developing 20, and expanding globally - The company possesses five human vaccine technology platforms: bacterial, viral, genetic engineering, combination vaccines, and mRNA42 - It owns four licensed vaccine manufacturing enterprises (Aimei Rongyu, Aimei Jianchi, Aimei Action, Aimei Chengxin) and three vaccine research institutes42 - Eight vaccine products targeting six diseases have been commercialized, with sales covering 31 provinces, municipalities, and autonomous regions in China, reaching over 2,000 county-level CDCs4245 - The company has 20 vaccine products in development, covering 12 disease areas, with the 13-valent pneumococcal conjugate vaccine and serum-free rabies vaccine having applied for marketing authorization4344 - In the first half of 2025, the quadrivalent meningococcal polysaccharide vaccine entered the African market, and the rabies vaccine debuted in the Central American market45 Our Products and R&D Pipeline Aimei Vaccine is a key player in China's vaccine industry, with 8 commercialized and 20 pipeline vaccines across 12 disease areas, rapidly advancing core products to market registration or late-stage clinical trials, and actively developing innovative platforms like mRNA Our Vaccine Products This section highlights the company's commercialized vaccine portfolio, detailing key features and market positioning of each product - Recombinant Hepatitis B Vaccine (Hansenula polymorpha): The first and only domestic producer using Hansenula polymorpha for stable batch release, featuring patented technology; the 10μg dose is the market's only yeast-derived HBV vaccine for all ages, and the 20μg dose is the only 0.5ml small-volume product in China515254 - Freeze-dried Human Rabies Vaccine (Vero cell): The second-largest market supplier, maintaining a 100% batch release pass rate for 18 years, with future plans for serum-free, high-titer human diploid, and mRNA rabies vaccine iterations5556 - Inactivated Hepatitis A Vaccine (Human Diploid Cell): Two specifications developed, with pre-filled syringe production resumed in 2022 and GMP compliance inspection passed57 - Meningococcal Polysaccharide Vaccine (Groups A, C, Y, and W135) (MPSV4): Launched in 2020, exceeding national standards on key quality indicators, free of antibiotics or preservatives, with a three-year shelf life, and a quadrivalent conjugate meningococcal vaccine (MCV4) under development58 Our Pipeline Vaccines This section details the company's extensive R&D pipeline, showcasing various vaccine candidates across different technology platforms and clinical stages | Technology Platform | Indication | Pipeline Vaccine | Self-developed/Co-developed | Pre-clinical | CTA | Phase I | Phase II | Phase III | Drug Registration Certificate Application & Approval | | :--- | :--- | :--- | :--- | :--- | :--- | :--- | :--- | :--- | :--- | | Bacterial Vaccines | Pneumococcal Disease | 13-valent Pneumococcal Conjugate Vaccine (PCV13) | Self-developed | | | | | | Marketing Authorization Application Submitted | | | | 20-valent Pneumococcal Conjugate Vaccine (PCV20) | Self-developed | | | | | | Clinical Trial Application Submitted | | | | 24-valent Pneumococcal Conjugate Vaccine (PCV24) | Self-developed | CTA Submission Planned for 2026 | | | | | | | | | 23-valent Pneumococcal Polysaccharide Vaccine (PPSV23) | Self-developed | Pre-application for Marketing Authorization Planned for 2025 | | | | | | | | Meningococcal Disease | Quadrivalent Conjugate Meningococcal Vaccine (MCV4) | Self-developed | | | | Phase II Clinical Trial Ongoing | | | | | | Hexavalent Meningococcal Vaccine | Self-developed | Pre-clinical Research | | | | | | | | Group B Streptococcus Disease | Hexavalent Group B Streptococcus Polysaccharide Conjugate Vaccine | Self-developed | CTA Submission Planned for 2026 | | | | | | | | Tetanus | Adsorbed Tetanus Vaccine | Self-developed | | Clinical Approval Obtained | | | | | | | Hib Infection | Haemophilus influenzae type b (Hib) Conjugate Vaccine | Self-developed | | Clinical Approval Obtained | | | | | | | Hand-Foot-and-Mouth Disease | EV71-CA16 Bivalent Hand-Foot-and-Mouth Disease Vaccine (Human Diploid Cell) | Self-developed | | | Phase I Planned for 2025 | | | | | Viral Vaccines | Influenza | Quadrivalent MDCK Cell Influenza Virus Vaccine | Self-developed | | Clinical Approval Obtained | | | | | | | Rabies | Serum-free Iterative Rabies Vaccine | Self-developed | | | | | | Marketing Authorization Application Submitted | | | | Novel High-titer Human Diploid Rabies Vaccine | Self-developed | | | | | Phase III Clinical Trial Ongoing | | | | Rabies | mRNA Iterative Rabies Vaccine | Self-developed | Clinical Trial Application Under Review | | | | | | | | Shingles | mRNA Shingles Vaccine | Self-developed | | Clinical Approval Obtained (China & US) | | | | | | mRNA Vaccines | Respiratory Syncytial Virus Infection | mRNA Respiratory Syncytial Virus RSV Vaccine | Self-developed | | Clinical Approval Obtained (China & US) | | | | | | | Influenza | mRNA Influenza Vaccine | Self-developed | Pre-clinical Research | | | | | | | Combination Vaccines | DTP | Acellular Diphtheria, Tetanus, Pertussis, Haemophilus influenzae type b, Quadrivalent Meningococcal Conjugate (DTcP-Hib-Mcv4) Combination Vaccine | Self-developed | Pre-clinical Research | | | | | | | | | Adsorbed Acellular Diphtheria, Tetanus, Pertussis (Component) Combination Vaccine (DTcP) | Self-developed | CTA Submission Planned for 2026 | | | | | | | Genetic Engineering Vaccines | Meningococcal Disease | Recombinant Meningococcal Group B Vaccine | Self-developed | Pre-clinical Research | | | | | | - Iterative upgrade of pneumococcal vaccine products: 13-valent pneumococcal conjugate vaccine (PCV13) has submitted a marketing authorization application and completed on-site verification; 23-valent pneumococcal polysaccharide vaccine has completed Phase III clinical serological testing; 20-valent pneumococcal conjugate vaccine has submitted a clinical trial application; and 24-valent pneumococcal conjugate vaccine has completed pre-clinical research6061626364 - Iterative upgrade of rabies vaccine products: Serum-free iterative rabies vaccine has submitted a marketing authorization application; novel high-titer human diploid rabies vaccine is undergoing Phase III clinical trials; and mRNA iterative rabies vaccine is under development6566676869 - Iterative upgrade of mRNA vaccine technology platform and products: mRNA iterative rabies vaccine, mRNA RSV vaccine, and mRNA shingles vaccine have all made significant progress, with mRNA RSV and shingles vaccines having obtained clinical trial approvals in both China and the US707172 - Progress on other pipeline vaccine products: Quadrivalent conjugate meningococcal vaccine (MCV4) has completed full vaccination for all subjects in Phase II clinical trials, and the EV71-CA16 bivalent hand-foot-and-mouth disease vaccine has been approved for Phase I clinical trials7374 - Vaccine development platform technologies and in-house R&D team: Possesses five validated human vaccine platform technologies, including innovative technologies like mRNA and genetic engineering, and is exploring AI-assisted vaccine R&D7576 Production All Aimei Vaccine products are self-produced by its four licensed factories, all GMP-certified by the NMPA, equipped with advanced machinery to ensure stable, high-quality vaccine supply - All vaccine products are self-produced by the company's four licensed factories and have passed NMPA's GMP inspections77 Production Facilities | Name | Location | Building Area (sqm) | Production Capacity (million doses) | Responsible Products | Production Lines | | :--- | :--- | :--- | :--- | :--- | :--- | | Aimei Rongyu Licensed Factory | Ningbo, Zhejiang Province | 25,318 | 25.0 | Freeze-dried Human Rabies Vaccine (Vero cell) | Two | | Aimei Chengxin Licensed Factory | Dalian, Liaoning Province | 11,877 | 45.0 | Recombinant Hepatitis B Vaccine (Hansenula polymorpha) | One | | Aimei Action Licensed Factory | Taizhou, Jiangsu Province | 18,711 | 5.3 | Inactivated Hepatitis A Vaccine | One | | Aimei Jianchi Licensed Factory | Ningbo, Zhejiang Province | 72,313 | 16.0 | Inactivated Hemorrhagic Fever with Renal Syndrome Vaccine, Mumps Vaccine, and MPSV4 | Three | Industry Overview China's vaccine market entered a new phase post-Vaccine Administration Law, reaching over RMB 101.77 billion (excluding COVID-19 vaccines) in 2024 with a 9.8% CAGR, facing economic downturns, anti-corruption, and declining birth rates, yet innovative vaccines offer significant advantages and pricing gaps with Western markets present strategic upgrade opportunities - China's vaccine market size (excluding COVID-19 vaccines) exceeded RMB 101.77 billion in 2024, with a compound annual growth rate of 9.8%78 - The market faces multiple challenges, including macroeconomic downturns, anti-corruption in healthcare, and declining birth rates78 - Innovative vaccine products hold significant advantages, and the pricing gap between China and Europe/US for innovative products presents strategic opportunities for product iteration and upgrades79 - Hepatitis B vaccine immunization will shift towards the entire population, with the adult hepatitis B market expected to become a new growth opportunity81 - mRNA technology, due to its rapid R&D, high efficacy, and safety advantages, has become a key focus for global vaccine manufacturers, with broad market prospects82 - China's pneumococcal vaccine market is projected to reach RMB 24 billion by 2025, with high-valent PCV vaccines being the future development trend83 - China's rabies vaccine market is expected to grow to RMB 22 billion by 2030, with serum-free and mRNA rabies vaccines driving market growth84 - China's RSV vaccine market is projected to exceed RMB 15.4 billion by 2030, and the shingles vaccine market is expected to reach nearly RMB 20 billion by 20308586 Prospects and Outlook Aimei Vaccine's R&D pipeline aligns with national policies, with five validated technology platforms and rapid product advancement; the company has established an international business unit, expanding into African and Central American markets with MPSV4 and rabies vaccines, securing exclusive agency agreements, and plans to accelerate commercialization of key products, deepen Belt and Road cooperation, and leverage mRNA technology to overcome international vaccine R&D barriers - The R&D pipeline aligns with national policies, with five validated technology platforms and rapid advancement of related vaccine products88 - An international business department has been established to accelerate global expansion, with vaccine products now entering the global market89 - In the first half of 2025, the quadrivalent meningococcal polysaccharide vaccine entered the African market, and the rabies vaccine debuted in the Central American market89 - International commercialization is being prepared for the upcoming 13-valent pneumococcal conjugate vaccine and serum-free iterative rabies vaccine, with exclusive agency agreements reached with several countries in West Asia and Southeast Asia90 - Pipeline products including the 13-valent pneumococcal conjugate vaccine, quadrivalent conjugate meningococcal vaccine, RSV vaccine, and shingles vaccine are all high-priority WHO-certified or internationally scarce varieties91 - GMP workshops for iterative pneumococcal and rabies vaccine series have been built and meet international standards, preparing for post-launch global market entry93 - In the second half, the company will accelerate the commercialization of the 13-valent pneumococcal conjugate vaccine, serum-free iterative rabies vaccine, and 23-valent pneumococcal polysaccharide vaccine, deepen 'Belt and Road' cooperation, and leverage its proprietary mRNA technology platform to break through R&D barriers for internationally scarce vaccines94 Financial Review This section provides a detailed analysis of the company's financial performance, including revenue, costs, and key financial ratios Overview This overview states that the financial review is based on the financial information and notes contained in this announcement and should be read in conjunction - The financial review is based on the financial information and its notes presented in other sections of this announcement95 Revenue For H1 2025, the company's main business revenue was RMB 514.7 million, down 4.2% year-on-year, primarily due to decreased rabies vaccine revenue, with Class II vaccine sales declining and Class I sales slightly increasing | Vaccine Product Sales Revenue | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Class I Vaccine Sales Revenue | 55,876 | 54,100 | | Class II Vaccine Sales Revenue | 458,781 | 483,078 | | Total | 514,657 | 537,178 | - Main business revenue decreased by 4.2% year-on-year to RMB 514.7 million, primarily due to a decline in rabies vaccine revenue96 Cost of Sales For H1 2025, cost of sales was RMB 173.4 million, up 16.5% year-on-year, mainly due to inventory impairment losses - Cost of sales increased by 16.5% year-on-year to RMB 173.4 million97 - The primary reason was the provision for inventory impairment losses in the first half of 202597 Gross Profit and Gross Margin For H1 2025, gross profit was RMB 341.2 million, down 12.1% year-on-year; gross margin was 66.3%, a 6.0 percentage point decrease, mainly due to inventory impairment losses - Gross profit decreased by 12.1% year-on-year to RMB 341.2 million98 - Gross margin decreased by 6.0 percentage points year-on-year to 66.3%98 - The main reason for the decline in gross margin was the provision for inventory impairment losses; excluding this factor, gross margin slightly increased98 Other Income and Gains For H1 2025, other income and gains were RMB 10.5 million, down 21.4% year-on-year, primarily due to reduced deposit interest income - Other income and gains decreased by 21.4% year-on-year to RMB 10.5 million99 - The primary reason was a decrease in deposit interest income in the first half of 202599 Research and Development Expenses For H1 2025, R&D expenses were RMB 107.0 million, a significant 37.1% year-on-year decrease, mainly due to the absence of overseas clinical trial expenses present in H1 2024 | Nature | 2025 (RMB thousands) | 2024 (RMB thousands) | | :--- | :--- | :--- | | Staff Costs | 36,966 | 46,198 | | Research Material Costs | 28,994 | 20,886 | | Professional Service Fees | 9,972 | 64,131 | | Depreciation and Amortization | 16,531 | 18,145 | | Utilities Costs | 9,793 | 13,866 | | Others | 4,706 | 6,884 | | Total | 106,962 | 170,110 | - Research and development expenses significantly decreased by 37.1% year-on-year to RMB 107.0 million101 - The primary reason was the absence of overseas clinical trial-related expenses in the first half of 2025, which were present in the first half of 2024101 Selling and Distribution Expenses For H1 2025, selling and distribution expenses were RMB 232.1 million, largely flat year-on-year, with a slight decrease of 0.1% - Selling and distribution expenses decreased by 0.1% year-on-year to RMB 232.1 million, largely consistent with the prior year period102 Administrative Expenses For H1 2025, administrative expenses were RMB 126.2 million, up 1.6% year-on-year, primarily due to a slight increase in depreciation and amortization expenses - Administrative expenses increased by 1.6% year-on-year to RMB 126.2 million103 - The primary reason was a slight increase in depreciation and amortization expenses in the first half of 2025103 Impairment Losses on Financial Assets For H1 2025, impairment losses on financial assets were RMB 7.6 million, an increase of RMB 3.7 million year-on-year, mainly due to increased bad debt provisions for accounts receivable - Impairment losses on financial assets increased by RMB 3.7 million year-on-year to RMB 7.6 million104 - The primary reason was an increase in the provision for doubtful debts on accounts receivable104 Finance Costs For H1 2025, finance costs were RMB 28.5 million, down 5.1% year-on-year, primarily due to reduced bank loan interest expenses - Finance costs decreased by 5.1% year-on-year to RMB 28.5 million105 - The primary reason was a decrease in bank loan interest expenses in the first half of 2025105 Income Tax Expense For H1 2025, the company received an income tax credit of RMB 15.6 million, up 11.4% year-on-year, primarily due to an increased loss before tax for a subsidiary - Income tax credit increased by 11.4% year-on-year to RMB 15.6 million106 - The primary reason was an increase in loss before tax for a subsidiary106 Loss for the Period For H1 2025, the company's loss was RMB 136.0 million, a 6.4% year-on-year reduction, primarily due to decreased R&D expenses - Loss for the period decreased by 6.4% year-on-year to RMB 136.0 million107 - The decrease in loss was primarily due to a year-on-year reduction in research and development expenses in the first half of 2025107 Cash and Cash Equivalents and Time Deposits As of June 30, 2025, cash and cash equivalents plus time deposits totaled RMB 401.9 million, down 32.4% from year-end 2024, mainly due to lower H1 collections and funds used for R&D and industrialization project final payments - Total cash and cash equivalents and time deposits decreased by 32.4% year-on-year to RMB 401.9 million108 - Reasons for the decrease include lower collections in the first half compared to the second half, and funds being used for ongoing R&D investments and final payments for industrialization projects108 Net Current Liabilities As of June 30, 2025, the company's net current liabilities were RMB 812.3 million, an increase of RMB 109.4 million from year-end 2024, mainly due to ongoing development expenditures and deferred development costs for multiple pipeline products; the company has secured sufficient working capital through renewed bank borrowings and unutilized bank facilities - Net current liabilities increased by RMB 109.4 million to RMB 812.3 million109 - The primary reasons are ongoing development expenditures for multiple pipeline products, as well as continuous investment in deferred development costs for the serum-free iterative rabies vaccine, 13-valent pneumococcal conjugate vaccine, and 23-valent pneumococcal polysaccharide vaccine109 - The company has renewed bank borrowings of RMB 128,000 thousands and has unutilized bank facilities of RMB 566,000 thousands, ensuring sufficient working capital109 Inventories As of June 30, 2025, inventory balance was RMB 433.9 million, down 6.2% from year-end 2024, primarily due to the company's inventory management efforts - Inventory balance decreased by 6.2% year-on-year to RMB 433.9 million110 - The primary reason was the company's inventory management, leading to a decrease in stock110 Trade Receivables As of June 30, 2025, the book value of trade receivables was RMB 1,165.0 million, up 3.7% from year-end 2024, primarily due to lower collections in the first half compared to the second half - The book value of trade receivables increased by 3.7% year-on-year to RMB 1,165.0 million111 - The primary reason was lower collections in the first half compared to the second half, leading to an increase in accounts receivable mid-year111 Capital Expenditures For H1 2025, capital expenditures were RMB 102.5 million, down 14.2% year-on-year, primarily for upgrading production, R&D, and quality equipment, payments for vaccine industrialization projects, and deferred development costs for pipeline vaccines; the decrease is mainly due to the 13-valent pneumococcal conjugate vaccine and serum-free iterative rabies vaccine entering the marketing review stage, reducing related investments - Capital expenditures decreased by 14.2% year-on-year to RMB 102.5 million112 - Primarily used for upgrading production, R&D, and quality equipment, vaccine industrialization projects, and deferred development costs for pipeline vaccines112 - The decrease is mainly due to the 13-valent pneumococcal conjugate vaccine and serum-free iterative rabies vaccine having entered the marketing review stage, leading to reduced related investments112 Borrowings and Gearing Ratio As of June 30, 2025, total financial liabilities were RMB 1,778.5 million, down 3.4% year-on-year, mainly due to reduced bank loan balances; the gearing ratio was 50.2%, a 0.8 percentage point decrease - Total financial liabilities decreased by 3.4% year-on-year to RMB 1,778.5 million113 - The gearing ratio decreased by 0.8 percentage points year-on-year to 50.2%113 - The primary reason was a decrease in bank loan balances in the first half of 2025113 Pledged Assets As of June 30, 2025, some of the Group's bank loans are secured by pledges of buildings (net book value approximately RMB 240.7 million), leased land (net book value approximately RMB 69.9 million), and guarantees provided by the company and its subsidiaries - Some bank loans are secured by pledges of buildings (net book value approximately RMB 240.7 million) and leased land (net book value approximately RMB 69.9 million)抵押担保114 - The company and its subsidiaries also provide guarantees114 Foreign Exchange Risk The Group's vast majority of business and all bank loans are transacted in RMB, thus posing no significant foreign exchange fluctuation risk, and currently, there is no hedging policy - The Group's vast majority of business and all bank loans are transacted in RMB, posing no significant foreign exchange fluctuation risk115 - Currently, there is no hedging policy, and no hedging transactions have been undertaken115 Contingent Liabilities As of June 30, 2025, the Group had no contingent liabilities with a material impact on its financial position or operating results - As of June 30, 2025, the Group had no material contingent liabilities116 Corporate Governance and Other Information This section covers the company's governance practices, compliance with codes, and other relevant corporate disclosures Dissolution of Supervisory Committee and Retirement of Supervisors The Supervisory Committee was dissolved on May 20, 2025, with all supervisors retiring from that date - The Supervisory Committee was dissolved, and all supervisors retired on May 20, 2025117 Standard Code for Securities Transactions by Directors The company has established a code of conduct for directors' securities dealings, and all directors confirmed compliance during the reporting period - The company has adopted a code of conduct for directors' securities transactions, and all directors confirmed compliance118 Corporate Governance Code The company complied with the Corporate Governance Code during the period, but the Chairman and CEO roles are combined, an arrangement the Board believes aids strategy execution and information flow, subject to timely review - The company complied with the Corporate Governance Code, but the roles of Chairman and Chief Executive Officer are held by Mr. Zhou Yan, which does not comply with code provision C.2.1119120 - The Board believes this arrangement facilitates strategic execution and information flow between management and the Board, and will review it at an appropriate time120 Purchase, Sale or Redemption of the Company's Listed Securities For the six months ended June 30, 2025, neither the company nor its subsidiaries purchased, sold, or redeemed any listed securities, and the company held no treasury shares - For the six months ended June 30, 2025, neither the company nor its subsidiaries purchased, sold, or redeemed any listed securities121 - As of June 30, 2025, the company held no treasury shares121 Employees and Remuneration Policy As of June 30, 2025, the company had approximately 1,493 employees, with total employee benefit expenses of RMB 166.9 million; remuneration policy is based on performance, skills, qualifications, experience, and industry practice, including an employee share incentive scheme - As of June 30, 2025, the company had approximately 1,493 employees (2024: 1,557 employees)122 - Total employee benefit expenses for the first half of 2025 were RMB 166.9 million (2024: RMB 180.4 million)122 - The remuneration policy is based on employee performance, skills, qualifications, experience, and industry practice, and includes an employee share incentive scheme122123 Material Investments, Acquisitions and Disposals For the six months ended June 30, 2025, the company had no material investments, significant acquisitions, or disposals of subsidiaries, associates, or joint ventures - For the six months ended June 30, 2025, the company had no material investments, significant acquisitions, or disposals124 Future Plans for Material Investments and Capital Assets As of the date of this announcement, the Group has no future plans involving material investments or capital assets - As of the date of this announcement, the Group has no future plans for material investments or capital assets125 Placement of New H Shares Under General Mandate and Use of Net Proceeds from Placement The company completed an H-share placement in February 2025, issuing 15,500,000 shares with net proceeds of approximately HKD 75.0 million, primarily allocated to R&D (60%), new product marketing (20%), and working capital (20%), with all remaining funds expected to be utilized by June 30, 2026 - On February 28, 2025, the company entered into an agreement with placing agents to place 15,500,000 H shares, with the placement completed on March 6, 2025126 - The net proceeds from the placement were approximately HKD 75.0 million (approximately RMB 71,638 thousands)127 Use of Net Proceeds from Placement | Intended Use | Approximate Percentage of Total Net Proceeds | Net Proceeds (HKD millions) | Amount Utilized as of June 30, 2025 (HKD millions) | Amount Unutilized as of June 30, 2025 (HKD millions) | | :--- | :--- | :--- | :--- | :--- | | Accelerate R&D of Product Pipeline | 60.0% | 45.0 | 26.0 | 19.0 | | Marketing and Commercialization of New Products | 20.0% | 15.0 | 6.7 | 8.3 | | Working Capital and Other Corporate Purposes | 20.0% | 15.0 | 14.6 | 0.4 | | Total | 100% | 75.0 | 47.3 | 27.7 | - All remaining unutilized net proceeds are expected to be fully utilized by June 30, 2026128 Interim Dividend The Board did not declare any interim dividend for the six months ended June 30, 2025 - The Board did not declare any interim dividend for the six months ended June 30, 2025129 Audit Committee The Audit Committee comprises three independent non-executive directors, with Professor Ker Wei PEI as Chairman, and has reviewed the Group's unaudited interim condensed consolidated financial information for the six months ended June 30, 2025 - The Audit Committee consists of three independent non-executive directors, with Professor Ker Wei PEI serving as Chairman130 - The Committee has reviewed the Group's unaudited interim condensed consolidated financial information for the six months ended June 30, 2025130 Material Events After Reporting Period As of the date of this announcement, no material events have occurred after the reporting period - As of the date of this announcement, no material events have occurred after the reporting period131 Publication of Interim Results Announcement and Interim Report This results announcement has been published on the HKEX and company websites, and the interim report will be published and dispatched to shareholders in due course - The results announcement has been published on the HKEX website and the company's website132 - The interim report will be published and dispatched to shareholders in due course132 Definitions This section provides definitions for key terms and abbreviations used throughout the report to ensure accurate understanding - This section provides definitions for key terms and abbreviations used throughout the report to ensure accurate understanding of its content133134135136137140