证券代码：300759 证券简称：康龙化成 公告编号：2024-056 康龙化成（北京）新药技术股份有限公司 第三届监事会第八次会议决议公告 本公司及监事会全体成员保证信息披露内容的真实、准确和完整，没有虚假 记载、误导性陈述或重大遗漏。 一、监事会会议召开情况 康龙化成（北京）新药技术股份有限公司（以下简称"公司"）第三届监事 会第八次会议于 2024 年 8 月 27 日以通讯方式召开，本次会议通知于 2024 年 8 月 23 日以邮件形式向全体监事发出。会议应出席监事 3 名，实际出席监事 3 名。 本次会议由监事会主席 Kexin Yang 博士主持，公司董事会秘书列席了本次会议。 本次会议的召集和召开符合《中华人民共和国公司法》等有关法律、行政法规、 部门规章、规范性文件和《康龙化成（北京）新药技术股份有限公司章程》的规 定。 二、监事会会议审议情况 1 表决结果：3 票同意，0 票反对，0 票弃权。 （二）审议通过《关于拟续聘 2024 年度境内财务及内控审计机构的议案》 公司监事会同意续聘安永华明会计师事务所（特殊普通合伙）为公司 2024 年度境内财务及内控审计机构。 具体内容详见公司于同日 ...

Financial Performance - Revenue for the first half of 2024 reached $1.2 billion, representing a 15% year-over-year growth[2] - Net profit for the first half of 2024 was $180 million, a 12% increase compared to the same period last year[2] - Revenue for the first half of 2024 was RMB 5,604.46 million, a slight decrease of 0.63% year-over-year[15] - Net profit attributable to shareholders increased by 41.64% to RMB 1,113.40 million compared to the same period last year[15] - Adjusted non-IFRS net profit attributable to shareholders decreased by 25.93% to RMB 690.27 million[22] - The company expects full-year 2024 revenue to grow by 12-15%, reaching $2.5-2.6 billion[4] - Revenue from clients using multiple business segments accounted for 71.16% of total revenue, amounting to RMB 3,987.94 million[23] - Revenue from North American clients was RMB 3,668.22 million, accounting for 65.45% of total revenue, a slight decrease of 0.20% year-over-year[24] - Revenue from European clients (including the UK) increased by 9.98% to RMB 945.58 million, accounting for 16.87% of total revenue[24] - The company served over 2,200 global clients, with over 360 new clients contributing RMB 161.24 million, or 2.88% of total revenue[23] - Overseas subsidiaries delivered revenue of RMB 736.83 million, a 3.99% increase year-over-year, accounting for 13.15% of total revenue[25] - Laboratory services revenue for the first half of 2024 was 3,371.1768 million yuan, a slight decrease of 0.27% year-over-year, with a gross margin of 44.46%, down 0.59 percentage points[27] - CMC (small molecule CDMO) services revenue for the first half of 2024 was 1,175.7473 million yuan, a decrease of 6.04% year-over-year, with a gross margin of 28.30%, down 4.16 percentage points[28] - Clinical research services revenue for the first half of 2024 was 843.2694 million yuan, an increase of 4.73% year-over-year, with a gross margin of 12.55%, down 4.43 percentage points[30] - The company's large molecule and cell & gene therapy services generated revenue of 211.21 million yuan, a year-on-year increase of 5.49%, with Q2 2024 revenue reaching 119.78 million yuan, a 31.00% increase from Q1 2024[32] - The gross margin for large molecule and gene therapy CDMO services was -31.34% in H1 2024 due to ongoing construction and operational costs[32] - Revenue for the first half of 2024 was RMB 5,604,463,354.87, a slight decrease of 0.63% compared to the same period last year[48] - Operating costs increased by 3.96% to RMB 3,733,284,838.30, while sales expenses decreased by 3.02% to RMB 122,949,469.45[48] - R&D investment increased by 14.06% to RMB 207,797,841.87, reflecting the company's commitment to innovation[48] - Net cash flow from operating activities decreased by 14.10% to RMB 1,099,735,310.22, while net cash flow from financing activities saw a significant decrease of 825.39% to RMB -4,653,026,429.44[48] - Laboratory services accounted for the largest portion of revenue at RMB 3,371,176,816.35, with a gross margin of 44.46%[49] - CMC (small molecule CDMO) services revenue decreased by 6.04% to RMB 1,175,747,332.83, with a gross margin of 28.30%[49] - Clinical research services revenue increased by 4.73% to RMB 843,269,367.02, but the gross margin decreased by 4.43% to 12.55%[49] - The company's cash and cash equivalents decreased by 414.22% to RMB -3,506,304,159.12, primarily due to increased cash outflows from financing activities[48] - The company's investment income was RMB 634,095,077.59, accounting for 51.68% of total profit, mainly from the disposal of non-current financial assets and the redemption of convertible bonds[50] - Cash and cash equivalents decreased by RMB 350.63 million, a drop of 59.44% compared to the end of the previous year[52] - Accounts receivable increased by 1.01% to RMB 89 million, representing 9.48% of total assets[52] - Inventory increased by 1.34% to RMB 1.188 billion, accounting for 5.17% of total assets[52] - Fixed assets grew by 7.63% to RMB 7.398 billion, representing 32.17% of total assets[52] - Prepayments increased by RMB 8.2274 million, a rise of 46.20%, mainly due to increased prepayments for raw material procurement[52] - Long-term prepaid expenses increased by RMB 184.6683 million, a growth of 35.48%, primarily due to new operating lease property improvements[52] - Trading financial assets decreased by RMB 260.8939 million, a drop of 41.95%, mainly due to the redemption of low-risk bank wealth management products[52] - Long-term equity investment increased by 0.46% to RMB 734.2411 million, representing 3.19% of total assets[52] - The company's investment in the UK subsidiary, Kanglong (UK), accounted for 13.78% of the company's net assets, with a net profit of RMB 35.0722 million for the reporting period[54] - Total investment during the reporting period was RMB 2.7588 billion, an increase of 4.93% compared to the same period last year[57] - The company's financial assets measured at fair value had a total initial investment cost of 2,128,576,048.84 yuan, with a cumulative investment income of 573,579,951.29 yuan[58] - The company's other financial assets had an initial investment cost of 1,861,000,000.00 yuan, with a cumulative investment income of 10,888,387.92 yuan[58] - The company's other financial assets had an initial investment cost of 267,576,048.84 yuan, with a cumulative investment income of 562,691,563.37 yuan[58] - The company's financial derivatives had a cumulative fair value change of -27,649,894.23 yuan[58] - The company's entrusted wealth management products had a total amount of 132,500 million yuan, with an outstanding balance of 41,814.97 million yuan[60] - The company's forward foreign exchange contracts had an initial investment amount of 669,919.2 million yuan, with a fair value change of -5,180.51 million yuan[61] - The company's forward foreign exchange contracts had a final amount of 327,832.8 million yuan, accounting for 25.19% of the company's net assets at the end of the reporting period[61] - The company's actual loss from forward contracts and related foreign exchange transactions was 4,585.70 million yuan[61] - The company's financial derivatives are valued based on the market price of the USD/CNY spot rate at the end of each month[62] - The company's financial derivatives investment was approved by the board of directors on March 28, 2024, and by the shareholders' meeting on June 6, 2024[62] - Kanglong Chem (Ningbo) Technology Development Co., Ltd., a wholly-owned subsidiary, reported total assets of 2.297 billion yuan, net assets of 1.793 billion yuan, operating income of 871.86 million yuan, and net profit of 147.85 million yuan[66] Business Operations and Strategy - The company's CDMO business contributed $400 million, accounting for 33% of total revenue[2] - The company plans to expand its production capacity in the second half of 2024, with an investment of $200 million[4] - The number of active clients increased by 10% to 1,500, with 30% of revenue coming from new clients[2] - The company's gross margin remained stable at 35%, reflecting efficient cost management[2] - The company issued $300 million in zero-coupon convertible bonds due in 2026[7] - New orders signed in the first half of 2024 increased by over 15% year-over-year[22] - The company participated in 666 drug discovery projects in the first half of 2024, an increase of 16 projects year-over-year[27] - Laboratory services new orders increased by over 10% year-over-year, with biological sciences accounting for over 53% of laboratory services revenue[27] - CMC (small molecule CDMO) services new orders increased by over 25% year-over-year, with 78% of revenue coming from existing drug discovery service clients[28] - The company's laboratory services team consists of 9,377 employees, including nearly 6,000 laboratory chemistry researchers[28] - The company's CMC (small molecule CDMO) services team consists of 4,228 employees, with 695 drug molecules or intermediates involved in projects[29] - The company's clinical research services team consists of 3,899 employees, with a 96-bed early-stage clinical research center in Maryland, USA[31] - The number of ongoing clinical trial service projects reached 1,112, including 77 Phase III trials, 409 Phase I/II trials, and 626 other clinical trials[32] - The company provided efficacy determination and release services for 21 cell and gene therapy products from 17 clients, including 9 clinical-stage projects and 2 commercial projects[32] - The company's Carlsbad in vivo toxicology research center in California has been partially operational, supporting cell and gene therapy products, ophthalmic products, and medical devices[33] - The global biotech financing market showed signs of recovery, with increased funding for biotech companies, indicating a potential rebound in client demand[33] - The company's integrated platform offers end-to-end services from drug discovery to clinical development, with a strong presence in China, the US, and the UK[35] - The company's chemical technology platform covers the entire small molecule drug R&D process, from compound design to GMP-compliant commercial production[37] - The company's DMPK/ADME global service network includes advanced technologies like radioactive isotope analysis, enhancing its position as a leading integrated service provider[37] - Established a comprehensive drug discovery to clinical proof-of-concept integrated service platform, covering multiple disciplines such as drug molecule design, compound library synthesis, and clinical data statistics[38] - Built a domestic clinical research platform offering end-to-end services for Phase I-IV clinical development, enhancing competitiveness through internal growth and external acquisitions[38] - Developed a gene therapy "lab analysis-IND study-process development & production" integrated platform, including GLP/GCP/GMP-compliant facilities in the US and UK[40] - Operates 21 entities globally (11 overseas), leveraging international operations to provide customized services and solutions across key pharmaceutical regions[40] - Acquired advanced production equipment and leased a Singapore-based formulation factory, expanding global CDMO service capabilities[42] - Focused on innovation in chemical and biological technologies, including fluid chemistry, biocatalysis, and gene editing platforms[43] - Maintains a workforce of 18,241 R&D, production, and clinical service personnel across China, the UK, and the US as of June 30, 2024[44] - Strengthened international operations through strategic acquisitions, integrating top-tier talent and facilities into the integrated R&D service platform[41] - Collaborated with US-based clinical pharmacology teams to support domestic clients in filing IND applications and conducting first-in-human studies in the US[40] - Enhanced global service network by investing in PharmaGend and acquiring Strides Pharma Global's production assets in Singapore[42] - The company added over 360 new clients in the first half of 2024, with over 97% of revenue coming from repeat clients[46] - The company aims to strengthen its leadership in small molecule R&D services and expand into new drug fields such as oligonucleotides, peptides, antibodies, ADC, and cell and gene therapy products[69] - Kanglong Chem plans to enhance its CMC (small molecule CDMO) service competitiveness by integrating commercial capabilities in China, the UK, and the US, and improving resource utilization and production efficiency[69] - The company will focus on improving the integration of its clinical development platform, particularly enhancing collaboration between US and Chinese teams to support the global expansion of Chinese innovative drugs[70] - Kanglong Chem will continue to develop its large molecule and cell and gene therapy service platforms, expanding service content and increasing operational efficiency[70] - The company plans to strengthen talent acquisition and retention, particularly in drug R&D, and enhance internal training programs to support long-term sustainable development[71] - Kanglong Chem will further enhance the synergy of its integrated platform by improving management efficiency and reducing costs[71] - The company will intensify its business and market development efforts, particularly in overseas markets, by deepening customer relationships and expanding service offerings[72] - Kanglong Chem will prioritize production safety and intellectual property security, ensuring high-quality products and services while adhering to international quality standards[73] - The company plans to deepen its CRO+CDMO integrated platform and expand its customer base to strengthen its competitive position[79] - The company will invest heavily in new technologies and consider acquisitions to enhance its service capabilities[80] - Maintaining high service quality is crucial, as any failure could lead to client loss and reputational damage[80] Environmental, Social, and Governance (ESG) - The company's ESG initiatives reduced carbon emissions by 15% compared to the previous year[7] - The company's ESG rating was upgraded to AA, and it was included in the 2024 A-share listed companies ESG Excellence TOP100 and Corporate Governance (G) Dimension Best Practice TOP20[26] - The company adheres to environmental protection laws and regulations in China, the UK, and the US, including the Clean Water Act and Clean Air Act[96] - Completed environmental self-acceptance for the application of biological in vitro test models to study drug efficacy and druggability platform project on April 13, 2023[98] - Obtained the first pollutant discharge permit on October 14, 2019, with the current permit valid until October 13, 2027[98] - Completed environmental self-acceptance for the new drug R&D outsourcing service base expansion project in Tianjin in November 2022[99] - Received approval for hazardous waste transfer to Hebei Province for utilization on January 24, 2024, with approval number Jinkaihuan Guzhuan [2024]10[100] - Received approval for hazardous waste transfer to Shandong Province for utilization on March 14, 2024, with approval number Jinkaihuan Guzhuan [2024]30[100] - Reapplied and obtained approval for the pollutant discharge permit on June 6, 2024[100] - Approved for the environmental impact assessment of the Xi'an R&D Center (Phase II) project on December 30, 2015, with approval number Jingkaihuan Pifu [2015]235[101] - Obtained the pollutant discharge permit for Xi'an on December 14, 2020, valid until December 13, 2023[101] - Completed environmental self-acceptance for the new drug R&D outsourcing platform expansion project in Beijing on August 20, 2020[97] - Approved for the environmental impact assessment of the new drug R&D outsourcing platform in vitro pharmacokinetics project on November 20, 2020, with approval number Jinghuan Shenzi [2020]0093[97] - The company completed the environmental protection acceptance monitoring report for the 120 tons/day laboratory wastewater treatment project at Kanglong Huacheng (Xi'an) New Drug Technology Co., Ltd., which was approved by the expert group[102] - The company obtained a pollutant discharge permit for Kanglong Huacheng (Xi'an) New Drug Technology Co., Ltd., valid until December 13, 2028[102] - The company completed the environmental impact assessment and acceptance monitoring reports for multiple projects in the Hangzhou Bay Life Science Park, including the bio-pharmaceutical R&D base and animal laboratory public service platform[103] - The company obtained environmental impact assessment approvals for the second phase of the Hangzhou Bay Life Science Industrial Park bio-pharmaceutical R&D service base project[103] - The company completed the environmental impact assessment and acceptance monitoring reports for the annual production of 47 tons and 25 tons of pharmaceutical intermediates at Kanglong Huacheng (Shaoxing) Pharmaceutical Co., Ltd.[104] - The company obtained a pollutant discharge permit for Kanglong Huacheng (Shaoxing) Pharmaceutical Co., Ltd., valid until October 10, 2026[104] - The company completed the environmental protection facility acceptance report for the annual production of 25 tons of pharmaceutical intermediates at Kanglong Huacheng (Shaoxing) Pharmaceutical Co., Ltd.[105] - The company obtained environmental impact assessment approvals for the new drug development technology service platform project at Kanglong Huacheng (Beijing) Technology Development Co., Ltd.[106] - The company completed the environmental impact assessment and adjustment report for the innovation center bio-pharmaceutical innovation platform project at Kanglong Huacheng (Ningbo) Bio-pharmaceutical Co., Ltd.[106] - The company reported the discharge of major pollutants, including CODcr, PH, NH3-N, and SS, at Kanglong Huacheng (Beijing) New Drug Technology Co., Ltd., with no超标排放情况[107] - Average concentration of VOCs emissions is 1.435 mg/m³, with a total emission of 11.28 tons[108] - Average concentration of nitrogen oxides emissions is 17 mg/m³, with a total emission of 0.2737 tons[108] - Total emission of waste organic solvents is 2094.547 tons[108] - Total emission of contaminated waste packaging is 606.45 tons[108] - Total emission of waste activated carbon is 14.836 tons[108] - Total emission of waste silica gel is 64.676 tons[108] - Total emission of laboratory waste is 20.475 tons[108] - Total emission of waste oil is 0 tons[109] - Total emission of expired and invalid drugs is 0 tons[109] - Total emission of COD

香港交易及結算所有限公司及香港聯合交易所有限公司對本公告的內容概不負責，對其準確性 或完整性亦不發表任何聲明，並明確表示，概不對因本公告全部或任何部分內容而產生或因倚 賴該等內容而引致的任何損失承擔任何責任。 Pharmaron Beijing Co., Ltd. 康 龍 化 成（ 北 京 ）新 藥 技 術 股 份 有 限 公 司 （於中華人民共和國註冊成立的股份有限公司） （股份代號：3759） 就2024年第一次臨時股東大會 暫停辦理股份過戶登記手續 康龍化成（北京）新藥技術股份有限公司（「本公司」）董事會謹此宣佈，為釐定有 權出席謹定於2024年9月13日（星期五）下午2時30分舉行的2024年第一次臨時股 東大會（「臨時股東大會」），並於會上投票的本公司H股（「H股」）股東名單，本公 司將於2024年9月10日（星期二）至2024年9月13日（星期五）期間（包括首尾兩日） 暫停辦理H股股份過戶登記手續，該期間將不會辦理H股股份過戶登記手續。於 2024年9月10日（星期二）名列本公司股東名冊的H股股東將有權出席臨時股東大 會並於會上投票。 為符合資格出席臨時股東大會並於會上投票，所有H股過戶文件連同有 ...

证券代码：300759 证券简称：康龙化成 公告编号：2024-052 康龙化成（北京）新药技术股份有限公司 关于参与私募股权投资基金的进展公告 本公司及董事会全体成员保证信息披露的内容真实、准确、完整，没有虚 假记载、误导性陈述或重大遗漏。 一、交易背景概述 为充分运用专业投资基金在行业内项目收集、研判的能力，提高公司投资能 力，康龙化成（北京）新药技术股份有限公司（以下简称"公司"或"康龙化成"） 以自有资金认缴出资人民币 10,000 万元作为有限合伙人参与投资无锡阿斯利康 中金创业投资合伙企业（有限合伙）（以下简称"阿斯利康基金" 或"合伙企 业 " ） 。 具 体 内 容 详 见 2020 年 10 月 20 日 公 司 在 巨 潮 资 讯 网 （http://www.cninfo.com.cn）披露的《关于参与投资无锡阿斯利康中金创业投资 合伙企业（有限合伙）的公告》（公告编号：2020-087）。 2021 年 1 月 28 日，阿斯利康基金已根据《证券投资基金法》和《私募投资 基金监督管理暂行办法》等法律法规的要求在中国证券投资基金业协会完成基金 的备案手续，并取得《私募投资基金备案证明》。具 ...

香港交易及結算所有限公司及香港聯合交易所有限公司對本公告的內容概不負責，對其準確性 或完整性亦不發表任何聲明，並明確表示概不就因本公告全部或任何部分內容而產生或因倚賴 該等內容而引致的任何損失承擔任何責任。 中華人民共和國，北京 2024年8月14日 Pharmaron Beijing Co., Ltd. 康 龍 化 成（ 北 京 ）新 藥 技 術 股 份 有 限 公 司 董事會會議通告 康龍化成（北京）新藥技術股份有限公司（「本公司」）董事會（「董事會」）謹此宣 佈，董事會會議將於2024年8月27日（星期二）舉行，藉以（其中包括）審議及批准 本公司及其附屬公司截至2024年6月30日止六個月之中期業績及其發佈。 承董事會命 康龍化成（北京）新藥技術股份有限公司 主席 樓柏良博士 （於中華人民共和國註冊成立的股份有限公司） （股份代號：3759） 於本公告日期，董事會包括執行董事樓柏良博士、樓小強先生及鄭北女士；非執 行董事胡柏風先生及李家慶先生；獨立非執行董事周其林先生、李麗華女士、曾 坤鴻先生及余堅先生。 ...

本公司及董事会全体成员保证信息披露的内容真实、准确、完整，没有虚假记 载、误导性陈述或重大遗漏。 康龙化成（北京）新药技术股份有限公司（以下简称"公司"）于 2024 年 6 月 6 日召开的 2023 年年度股东大会、2024 年第一次 A 股类别股东大会及 2024 年第一次 H 股类别股东大会审议通过了《关于增加注册资本、修订<公司章程> 的议案（一）》《关于增加注册资本、修订<公司章程>的议案（二）》。 近日，公司办理完成相关内容的工商变更登记手续，并取得了北京经济技术 开发区市场监督管理局换发的《营业执照》。公司新换发的《营业执照》基本信 息如下： 统一社会信用代码：9111030276350109XG 名称：康龙化成（北京）新药技术股份有限公司 类型：股份有限公司（中外合资、上市） 证券代码：300759 证券简称：康龙化成 公告编号：2024-051 康龙化成（北京）新药技术股份有限公司 关于完成工商变更登记并换发营业执照的公告 成立日期：2004 年 07 月 01 日 营业期限：2004 年 07 月 01 日至长期 住所：北京市北京经济技术开发区泰河路 6 号 1 幢八层 经营范围：药用化 ...

康龙化成（北京）新药技术股份有限公司 关于追加投资境外参股公司暨关联交易的公告 本公司及董事会全体成员保证信息披露的内容真实、准确、完整，没有虚假记 载、误导性陈述或重大遗漏。 一、关联交易背景概述 证券代码：300759 证券简称：康龙化成 公告编号：2024-050 2023 年 10 月 18 日，康龙化成（北京）新药技术股份有限公司（以下简称 "公司"）召开了第三届董事会第三次会议和第三届监事会第三次会议，分别审 议通过了《关于投资参股境外公司暨关联交易的议案》，同意公司以自有资金 1,050 万美元通过全资子公司 Pharmaron (Hong Kong) International Limited（以下 简称"康龙香港国际"）与合作方 CMS MEDICAL VENTURE PTE. LTD.（以下简 称"康哲药业"）、Rxilient Health Pte. Ltd.（以下简称"康联达"）、HEALTHY GOAL LIMITED（以下简称"君联基金"）共同投资位于新加坡的 Rxilient Biohub Pte. Ltd. （现更名为 PharmaGend Global Medical Ser ...

股份發行人及根據《上市規則》第十九B章上市的香港預託證券發行人的證券變動月報表 截至月份: 2024年7月31日 狀態: 新提交 致：香港交易及結算所有限公司 公司名稱: 康龍化成（北京）新藥技術股份有限公司 (於中華人民共和國註冊成立的股份有限公司） 呈交日期: 2024年8月5日 I. 法定/註冊股本變動 | 1. 股份分類 | 普通股 | 股份類別 | H | | 於香港聯交所上市 (註1) | | 是 | | | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 證券代號 (如上市) | 03759 | 說明 | H股 | | | | | | | | | 法定/註冊股份數目 | | | 面值 | | 法定/註冊股本 | | | 上月底結存 | | | 301,537,125 | RMB | | 1 RMB | | 301,537,125 | | 增加 / 減少 (-) | | | 0 | | | RMB | | 0 | | 本月底結存 | | | 301,537,125 | RMB | | 1 RMB | | 301,537,125 | | ...

2024 年 5 月 8 日至 2024 年 7 月 25 日，公司通过股份回购专用证券账户使 用自有资金以集中竞价交易方式回购股份，回购股份数量为 9,608,288 股，占公 司目前总股本（1,787,394,297 股）的 0.54%，回购的最高成交价为 22.27 元/股， 最低成交价为 17.89 元/股，成交总金额为 200,092,209.11 元（不含交易费用）。 截至本公告披露之日，公司本次回购股份方案回购期限届满。 二、回购股份实施情况与回购股份方案不存在差异的说明 证券代码：300759 证券简称：康龙化成 公告编号：2024-049 康龙化成（北京）新药技术股份有限公司 关于股份回购结果暨股份变动的公告 本公司及董事会全体成员保证信息披露内容的真实、准确和完整，没有虚假 记载、误导性陈述或重大遗漏。 康龙化成（北京）新药技术股份有限公司（以下简称"公司"）于 2024 年 4 月 25 日召开的第三届董事会第七次会议审议通过了《关于回购公司 A 股股份 方案的议案》，公司计划使用不低于人民币 2 亿元且不超过人民币 3 亿元（均包 含本数）的自有资金以集中竞价交易方式回购公司已发行的人 ...

Investment Rating - Buy (Maintained) [2] Core Views - The company's revenue for H1 2024 is expected to be between 5.471-5.640 billion yuan, a year-on-year decline of 0%-3% [3] - Net profit attributable to the parent company is expected to be 1.055-1.143 billion yuan, a year-on-year increase of 34%-45% [3] - Adjusted net profit is expected to be 671-718 million yuan, a year-on-year decline of 23%-28% [3] - Q2 2024 revenue is estimated at 2.885 billion yuan, a quarter-on-quarter increase of 8.01% [3] - Q2 2024 net profit attributable to the parent company is expected to be 868 million yuan, a year-on-year increase of 98.35% and a quarter-on-quarter increase of 276.67% [3] - Adjusted net profit for Q2 2024 is expected to be 355 million yuan, a year-on-year decline of 28.05% and a quarter-on-quarter increase of 4.90% [3] - The company's long-term development is promising, with projected net profits for 2024-2026 at 1.784, 2.003, and 2.398 billion yuan, respectively [3] - EPS for 2024-2026 is forecasted at 1.00, 1.12, and 1.34 yuan, respectively [3] - The current PE ratio is 20.0, 17.9, and 14.9 times for 2024-2026, respectively [3] Business Performance - New orders in H1 2024 increased by over 15% year-on-year [4] - Laboratory services revenue reached a historical high in Q2 2024 due to the recovery in new orders [4] - CMC service revenue increased quarter-on-quarter in Q2 2024, with more projects expected to be delivered and recognized in H2 2024 [4] - Clinical research services, as well as macromolecular and cell and gene therapy services, saw both quarter-on-quarter and year-on-year revenue growth [4] Non-Recurring Gains - Non-recurring gains attributable to shareholders in H1 2024 were approximately 610-660 million yuan [5] - The sale of the company's stake in PROTEOLOGIX to Johnson & Johnson for approximately 102 million USD contributed 560 million yuan to non-recurring gains [5] - Other non-recurring gains included convertible bond redemptions, government subsidies, and financial product income [5] Financial Forecasts - Revenue for 2024-2026 is projected to be 12.848, 14.752, and 17.327 billion yuan, respectively [6] - Net profit attributable to the parent company for 2024-2026 is forecasted at 1.784, 2.003, and 2.398 billion yuan, respectively [6] - Gross margin for 2024-2026 is expected to be 34.7%, 34.5%, and 35.2%, respectively [6] - Net margin for 2024-2026 is projected at 13.6%, 13.3%, and 13.6%, respectively [6] - ROE for 2024-2026 is forecasted at 12.0%, 12.3%, and 13.2%, respectively [6] Market Data - Current stock price: 20.01 yuan [7] - Total market capitalization: 35.766 billion yuan [7] - Circulating market capitalization: 28.586 billion yuan [7] - Total shares outstanding: 1.787 billion [7] - Circulating shares: 1.429 billion [7] - Turnover rate in the last 3 months: 80.01% [7]