【江苏：新增A股上市公司全国第一】 铜锣一响，黄金万两。12月31日上午9:30分，苏州市新广益电子股份有限公司正式登陆深交所。至此，江苏全年新增A股上市公司 达到29家，数量位居全国第一。 岁末年终，江苏各行各业也传来"捷报"：全年新增A股上市公司数量全国第一、创新药获批数连续三年领跑全国……一项项亮眼数 据描绘出江苏高质量发展"多点开花"的生动图景。 回顾整个2025年，江苏月月有企业上市。从区域来看，苏州（12家）、无锡（5家）、常州（3家）分列前三。从行业来看，以制 造业为主，其中27家为战略性新兴产业。截至目前，苏企在科创板（115家）、北交所（56家）数量保持全国第一。 江苏省金融研究院副院长骆祖春说："上市企业代表着一个地方区域经济发展健康的水平。江苏全省都对企业上市工作非常重视， 对进入上市企业培育库的企业提供全生命周期的服务，推动创新链产业链资金链人才链深度融合，最终更好提升区域经济活力。" 正大天晴药业集团总裁助理刘亮说："'库莫西利'胶囊获批，向外界证明了中国有能力在乳腺癌治疗的前沿机制上跑出'全球首创'， 完成了从'跟随式竞争'到'机制突破的引领'关键转变。" 【乘风破浪 江苏造船业加 ...

Investment Rating - The report does not explicitly provide an investment rating for the biopharmaceutical sector [5]. Core Insights - The biopharmaceutical sector is experiencing significant activity with multiple companies focusing on innovative drug development, particularly in the area of siRNA targeting INHBE, which shows promise for fat reduction without muscle loss [3][24]. - The report highlights the recent performance of new drug stocks, with notable gains from companies such as Saint Nor Pharmaceutical (+30.88%) and Dongyao Pharmaceutical (+16.37%), while companies like Kexin Pharmaceutical (-14.19%) and Rongchang Biotechnology (-10.09%) faced declines [1][15]. - There is an expectation of multiple catalysts in the sector, including academic conferences and data releases, which could drive further interest and investment [2]. Weekly New Drug Market Review - From December 8 to December 14, 2025, the new drug sector saw significant stock movements, with the top five gainers and losers listed [1][15]. - The report notes that there were no new drug approvals during this week, but 11 new drug applications were accepted [4][31]. Weekly New Drug Industry Analysis - Wave Life Sciences has reported promising initial data for its siRNA drug WVE-007, which targets INHBE and demonstrates potential for reducing visceral fat while preserving muscle mass [3][24]. - The report indicates that several companies, both globally and domestically, are actively developing siRNA drugs targeting INHBE, with five drugs already in clinical development [27][28]. Weekly New Drug Approval & Acceptance Status - No new drug or new indication approvals were reported this week, but 11 new drug applications were accepted [4][31]. - A total of 55 new drug clinical applications were approved, and 47 new drug clinical applications were accepted during the week [9][34]. Key Events in Domestic Market - Significant events include the approval of new drugs by companies such as Zhengda Tianqing and Nuo Cheng Jian Hua, which received approval for their respective new drugs [10][11]. Key Events in Overseas Market - Noteworthy overseas events include Eli Lilly's announcement of positive results from its TRIUMPH-4 Phase 3 trial and the FDA's approval of a gene therapy by Fondazione Telethon [11].

文/华夏大健康研究院 11月21日下午，由华夏时报社主办的"2025第五届华夏大健康产业发展暨康复服务大会"在北京成功举 行。本次大会以"智领健康未来"为主题，汇聚产业界、学术界、研究机构及投资方等多方代表，旨在整 合全链条资源，把脉行业趋势，探索发展路径。 2025年上半年，翰森制药收入74.34亿元，同比增长14.3%，其中创新药与合作产品销售收入为61.45亿 元，占总收入比例上升至82.7%，创新药已成为驱动本公司业绩可持续增长的核心动力。截至报告期 末，公司已有7款创新药在中国产生销售收入，其中9项适应症已纳入国家医保目录，使更多患者得到高 质量治疗的同时，切实大幅降低患者用药负担。 中国生物制药：全球首创，中国引领——库莫西利重磅来袭 中国生物制药自创立以来，始终专注于药物创新，坚持以患者需求为核心，致力于打造具备全球竞争力 的创新产品线，以健康科技温暖更多生命。在肿瘤治疗领域，我们持续深耕，不断取得重大突破。其 中，我们自主研发的1类新药"库莫西利"，作为全球首创的口服CDK2/4/6抑制剂，在针对内分泌经治的 HR+/HER2-晚期乳腺癌的Ⅲ期研究中，展现出卓越的疗效与安全性。该产品的临床研究 ...

Core Insights - The report emphasizes the significant role of phosphoramidite monomers in the small nucleic acid industry chain, highlighting their impact on the development of small nucleic acid drugs, which are considered promising candidates for treating various diseases due to their unique molecular structures and therapeutic mechanisms [1][6][10] - The report predicts robust growth in the demand for phosphoramidite monomers, with multinational pharmaceutical companies likely to benefit from this trend, as the global nucleotide market is projected to reach USD 730 million in 2023, with China being the largest production market [10][11] Section Summaries Phosphoramidite Monomer's Role - Phosphoramidite monomers are crucial raw materials for synthesizing small nucleic acid drugs, enhancing their stability and biological activity, and driving innovation in drug development [6][9] - The solid-phase phosphoramidite method is the mainstream technique for synthesizing oligonucleotides, which are a major cost component in nucleic acid drug production [9] Market Dynamics - The report notes that 90% of global nucleotides are used for nucleic acid drug production, with only about 10% allocated to health foods and agriculture [10] - The small nucleic acid drug market is primarily dependent on major multinational pharmaceutical companies, indicating potential benefits for companies within their supply chains [11] Investment Recommendations - The report suggests focusing on innovative drug companies such as Furuya Co., OncoOne, and others, as well as raw material suppliers like WuXi AppTec and others, indicating a diverse range of investment opportunities in the sector [10]

Core Viewpoint - October is Breast Cancer Awareness Month, emphasizing the importance of early prevention, detection, and treatment, particularly for HR-positive, HER2-negative advanced breast cancer patients [1][2]. Group 1: First-Line Treatment - The standard first-line treatment for HR-positive, HER2-negative advanced breast cancer is endocrine therapy combined with CDK4/6 inhibitors, which are crucial for effective tumor suppression [2]. - Endocrine therapy serves as the cornerstone of treatment, even in cases with visceral metastasis, with key drugs including tamoxifen and aromatase inhibitors [2]. - There are currently eight approved CDK4/6 inhibitors in China for HR-positive, HER2-negative breast cancer, including palbociclib and abemaciclib [2]. Group 2: Post-Resistance Strategies - Resistance to endocrine therapy does not signify the end of treatment; patients should undergo evaluations to identify the cause of resistance and find suitable alternative therapies [5]. - New treatment options are being explored, including novel CDK2/4/6 inhibitors like cumosilib, which have shown promising results in clinical trials, significantly extending progression-free survival [6][7]. - The PAM pathway (PI3K/Akt1/mTOR) is another target for therapy, with various inhibitors being developed to counteract its activation, which can lead to treatment resistance [8][9]. Group 3: Emerging Therapies - ESR1 mutations are common in patients treated with aromatase inhibitors and CDK4/6 inhibitors, leading to the development of selective estrogen receptor degraders (SERDs) as a new treatment option [10]. - Biomarkers such as HER2 and TROP2 can help identify patients who may benefit from antibody-drug conjugates (ADCs), providing targeted therapy to improve outcomes [11]. - The ongoing advancements in medical research and new drug developments offer hope for more effective treatments for HR-positive breast cancer patients [12].

Core Insights - The 2025 European Society for Medical Oncology (ESMO) annual meeting will take place in Germany from October 17 to 21, where several significant oral reports from domestic innovative pharmaceutical companies are expected to be disclosed [1] - China National Pharmaceutical Group is set to present key data on its CDK2/4/6 inhibitor, Kumosili, and HER2 dual-target ADC, TQB2102, highlighting its comprehensive coverage in the breast cancer treatment landscape [1] Industry Overview - Breast cancer is the second most common cancer globally, following lung cancer, and has the highest incidence and mortality rates among women [1] - The breast cancer market is highly competitive, particularly in the HR+/HER2- subtype, which accounts for approximately 65%-70% of all breast cancer cases [2] - The global market for CDK4/6 inhibitors is projected to approach $13 billion by 2024, with ongoing growth driven by products from Pfizer, Eli Lilly, and Novartis [2] Company Developments - Kumosili capsules, a new generation CDK2/4/6 inhibitor, are expected to receive approval for second-line treatment of HR+/HER2- locally advanced or metastatic breast cancer by the end of this year [3] - The company is also advancing its clinical trials for Kumosili in first-line and adjuvant settings, aiming for comprehensive coverage across treatment lines [3] - TQB2102, another product from China National Pharmaceutical Group, will present phase Ib clinical data for HER2-positive recurrent/metastatic breast cancer at ESMO [3] Competitive Landscape - The ADC market for HER2-positive breast cancer is evolving, with significant sales from existing products like DS-8201, which reached $3.8 billion last year and is projected to peak at $10 billion [4] - TQB2102 has been optimized in terms of target binding, toxin load, and payload compared to DS-8201, and has been recognized as a breakthrough therapy for multiple indications [4] - The company has a diverse pipeline covering various cancer types, including breast, colorectal, lung, bile duct, and gastric cancers, with several indications entering phase III clinical trials [4]

Core Viewpoint - The report from GF Securities initiates coverage on China Biopharmaceutical (01177) with a "Buy" rating, projecting EPS of 0.23, 0.26, and 0.28 CNY per share for 2025-2027, and a fair value of HKD 11.54 per share, highlighting the company's transformation from a generic drug manufacturer to an R&D-driven international pharmaceutical group [1][2]. Group 1 - The company has established a strong product matrix through self-research, mergers and acquisitions, and pipeline introductions, covering four core therapeutic areas: oncology, liver disease, respiratory system, and surgical/pain management [1][2]. - R&D investment has been increasing year-on-year from 2018 to the first half of 2025, with the R&D expense ratio rising from 9.9% to 18.1%, and R&D expenses reaching CNY 3.188 billion in the first half of 2025, with approximately 78% allocated to innovative drug development [2]. Group 2 - In the oncology field, key products include: - "Defu" combination therapy with Anlotinib, which is a flagship product, and its combination with anti-PD-(L)1 for first-line indications [2]. - HER2 dual antibody ADC TQB2102, which is leading globally and has entered Phase III for treating HER2 low-expressing and HER2-positive breast cancer [2]. - CDK2/4/6 inhibitor Kumosilib, a global first, has submitted for marketing approval for HR+/HER2- breast cancer [2]. - CCR8 monoclonal antibody LM-108, a global first, is currently in Phase II [2]. - In the respiratory field, PDE3/4 inhibitors are expected to become a blockbuster drug for COPD, with TQC3721 being in the second position globally [2]. - In the liver disease area, the pan-PPAR agonist Lanifibranor may become the first MASH drug in China, while FGF21 fusion protein could be the most effective MASH drug [2]. - In the surgical and pain management sector, the company has established four transdermal patch technology platforms, solidifying its position as a leader in transdermal formulations [2].

Core Viewpoint - GF Securities initiates coverage on China Biologic Products (01177) with a "Buy" rating, projecting EPS of 0.23, 0.26, and 0.28 CNY per share for 2025-2027, with a fair value of HKD 11.54 per share, highlighting the company's transformation from a generic drug manufacturer to an R&D-driven international pharmaceutical group [1][2] Group 1 - The company has established a strong product pipeline covering four core therapeutic areas: oncology, liver disease, respiratory system, and surgical/pain management, successfully transitioning from a generic drug company to an innovative pharmaceutical leader [1][2] - R&D investment has been increasing annually from 2018 to H1 2025, with the R&D expense ratio rising from 9.9% to 18.1%, and R&D expenses reaching CNY 3.188 billion in H1 2025, with approximately 78% allocated to innovative drug development [2] Group 2 - In the oncology field, key products include: - "DeFu" combination therapy with Anlotinib, which is a flagship product, expanding first-line indications through combination with anti-PD-(L)1 therapy, with approvals for SCLC, endometrial cancer, and renal cell carcinoma [2] - HER2 bispecific antibody ADC TQB2102, which is leading globally and is in Phase III for treating HER2 low-expressing and HER2-positive breast cancer [2] - CDK2/4/6 inhibitor Kumosi Li, the world's first of its kind, has submitted for marketing approval for HR+/HER2- breast cancer [2] - CCR8 monoclonal antibody LM-108, a global first, is currently in Phase II [2] Group 3 - In the respiratory field, PDE3/4 inhibitors are expected to become a blockbuster drug for COPD, with TQC3721 being in the second position globally [2] - In the liver disease area, the pan-PPAR agonist Lanifibranor may become the first MASH drug in China, while FGF21 fusion protein could be the most effective MASH drug [2] - In the surgical and pain management sector, the company has established four transdermal patch technology platforms, solidifying its position as a leader in transdermal formulations [2]

Group 1 - The company is covered for the first time by Guojin Securities, which gives a "buy" rating and forecasts revenue of 33.41 billion, 37.17 billion, and 41.70 billion yuan for 2025, 2026, and 2027 respectively, with year-on-year growth of +15.75%, +11.24%, and +12.21% [1] - The net profit attributable to the parent company is projected to be 4.63 billion, 4.75 billion, and 5.28 billion yuan for the same years, with year-on-year growth of +32.17%, +2.75%, and +11.17% [1] - The company has a solid position as a leading pharmaceutical player, with a steady increase in revenue and operating profit, and a significant rise in R&D investment, which accounted for 18.1% of revenue in H1 2025, up from 11.1% in 2020 [1] Group 2 - The company acquired Lixin Pharmaceutical for approximately 500 million USD, enhancing its oncology product pipeline [2] - The drug Anlotinib has been approved for 9 indications, and its combination with PD-1 has shown superior results in head-to-head trials against other treatments [2] - The company aims to license out innovative products as a key strategic goal, with promising candidates in oncology and respiratory fields, potentially generating recurring revenue from business development transactions starting in 2025 [3]

Core Viewpoint - Company is positioned as a leading player in the biopharmaceutical industry, with a strong focus on innovation and growth in revenue and profit margins [1][2][3] Group 1: Financial Projections - Company is expected to achieve revenues of 334.12 billion, 371.66 billion, and 417.04 billion CNY in 2025, 2026, and 2027 respectively, representing year-on-year growth of +15.75%, +11.24%, and +12.21% [1] - Projected net profit attributable to shareholders is 46.26 billion, 47.53 billion, and 52.84 billion CNY for the same years, with year-on-year growth of +32.17%, +2.75%, and +11.17% [1] - Earnings per share (EPS) are forecasted to be 0.25, 0.25, and 0.28 CNY for 2025, 2026, and 2027 [1] Group 2: Strategic Developments - Company has acquired Lixin Pharmaceutical for approximately 500 million USD, enhancing its oncology product pipeline [2] - The acquisition includes key products such as LM-299 and LM-305, which have been licensed to major pharmaceutical companies [2] - Anlotinib has been approved for 9 indications, showing promising results in head-to-head trials against competitors [2] Group 3: Innovation and R&D Focus - Company has significantly increased R&D investment, with 18.1% of revenue allocated to R&D in the first half of 2025, up from 11.1% in 2020 [1] - The number of approved innovative products has reached 19, with innovative product revenue accounting for 44.4% of total revenue in the first half of 2025 [1] - Company aims to leverage its innovative products, such as CDK2/4/6 inhibitors and HER2 bispecific antibodies, to establish a competitive edge in the international market [3]