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总投资超1亿元!深圳理工大学牵头项目获资助
Nan Fang Du Shi Bao· 2025-12-14 14:18
"'深圳市AI驱动医药研发公共服务平台组建项目'正是在这一背景下应运而生的。"深圳理工大学药学院院 长陈有海表示,该平台旨在构建覆盖药物研发全链条的公共技术服务平台,为高校、科研院所及医药企业 等提供AI辅助药物发现、优化与药效评估等一站式服务,助力降低研发成本与风险、缩短研发周期,提升 研发效率并加速成果转化。 深圳理工大学秉持"科教融汇、产教融合"理念,积极构建"基础研究—技术攻关—成果转化"体系,为平台 建设提供了坚实的智力支持和创新动力。技术层面,深圳理工大学依托学科交叉优势,组建跨领域研究团 队,为平台提供源头创新动力;协同层面,实现高校与企业深度联动,整合高校科研优势与企业产业资 源,形成了产学研融合的创新样本;人才方面,学校汇聚了一批国内外顶尖科研力量,在人工智能、生物 医药等领域取得了一系列重要成果。 复星医药作为国内领先的医药产业集团,拥有丰富的产业资源和强大的市场拓展能力。其在药物研发、生 产、销售等环节积累了丰富的经验,能够为平台提供实践应用场景和产业反馈,促进科研成果的快速转化 和商业化。 南都讯 记者伍曼娜近日,深圳市发展和改革委员会正式批复2025年第一批战略性新兴产业扶持计划拟资 ...
医药行业周报:医保商保双目录发布-20251214
Investment Rating - The report maintains a positive outlook on the pharmaceutical industry, recommending a focus on innovative drugs and sectors with improving performance, such as medical devices and upstream segments [3][4]. Core Insights - The pharmaceutical sector experienced a decline of 1.0% this week, ranking 17th among 31 sub-industries. The overall valuation of the pharmaceutical sector stands at 29.2 times earnings, placing it 10th among the primary industries [2][4][7]. - Key events include Fosun Pharma granting exclusive global rights for its oral GLP-1 drug to Pfizer, with potential total payments reaching $2.085 billion. Additionally, Eli Lilly's GLP-1/GIP/GCGR agonist Retatrutide showed promising Phase III clinical data, achieving a weight loss of 28.7% over 68 weeks [3][14][17]. - The report highlights significant mergers and acquisitions, such as Sobi's acquisition of Arthrosi for $950 million upfront and $550 million in milestone payments, and Zhaoli Pharmaceutical's planned acquisition of a multi-trace element injection asset group for approximately RMB 356 million [3][15][22]. Market Performance - The pharmaceutical index decreased by 1.0% this week, while the Shanghai Composite Index fell by 0.3%. The overall performance of the pharmaceutical sector was ranked 17th among 31 sub-industries [2][4][6]. - The report details the performance of various sub-sectors, with notable declines in medical circulation (-4.2%), offline pharmacies (-4.3%), and blood products (-4.1%), while medical R&D outsourcing saw an increase of 3.7% [7][11]. Recent Key Events - The report discusses recent business developments, including the approval of Shanghai Pharma's new drug, and the change of control at Tailong Pharmaceutical, which will now be under Jiang Pharmaceutical Holdings [20][22]. - It also notes the IPO application of Shiyao Innovation, which was accepted with a market value of RMB 47.9 billion, focusing on health-related sectors and innovative drugs [23]. Company Valuation - The report provides a valuation table for key companies in the pharmaceutical sector, indicating projected earnings per share (EPS) and price-to-earnings (PE) ratios for 2025 to 2027. For instance, Mindray Medical is projected to have a PE of 23 in 2025, while Hengrui Medicine is expected to have a PE of 48 [29].
复星医药(600196):再次牵手MNC 创新转型持续推进
Xin Lang Cai Jing· 2025-12-13 06:26
Core Viewpoint - Fosun Pharma's subsidiary, Yaoyou Pharmaceutical, has signed a licensing agreement with Pfizer for the exclusive global development, use, production, and commercialization rights of the oral small molecule GLP-1R agonist YP05002, indicating a significant step in the company's innovative transformation and strategic partnerships [1][2]. Group 1: Licensing Agreement Details - The agreement grants Yaoyou Pharmaceutical an upfront payment of $150 million, up to $350 million in development milestone payments, and up to $1.585 billion in sales milestone payments [1]. - Pfizer will pay royalties to Yaoyou Pharmaceutical based on the annual net sales of the licensed product, at a maximum percentage agreed upon [1]. Group 2: Clinical Trials and Licensing Transactions - As of December 9, 2025, YP05002 is in Phase I clinical trials in Australia [2]. - In 2025, Fosun Pharma completed three license-out transactions, including granting global rights (excluding Greater China) for FXS6837 to Sitala for an upfront payment of $25 million and potential total payments of $670 million, and for XH-S004 to Expedition for an upfront payment of $17 million and potential total payments of $645 million [2]. Group 3: Financial Targets and Incentives - The company has established long-term incentive mechanisms based on net profit attributable to shareholders (60% weight) and innovative drug revenue (40% weight), with targets set for 2025-2027 being net profits of 3.32 billion, 3.96 billion, and 4.77 billion yuan, and innovative drug revenues of 9.36 billion, 11.23 billion, and 13.48 billion yuan, reflecting a CAGR of approximately 20% [3]. Group 4: Revenue and Profit Forecasts - Due to the impact of volume-based procurement being slightly higher than expected, the company's revenue forecasts for 2025-2027 have been adjusted to 40.10 billion, 40.85 billion, and 45.58 billion yuan, down from previous estimates [4]. - The net profit forecasts for 2025-2027 have been revised upwards to 3.34 billion, 4.02 billion, and 4.84 billion yuan, supported by steady growth in innovative drug sales and unexpected licensing agreements [4].
20.85亿美元!复星医药国际合作再添里程碑
Ge Long Hui· 2025-12-13 04:35
Core Viewpoint - Pfizer's aggressive strategy in the weight loss drug market is underscored by its recent licensing agreement with Fosun Pharma, granting Pfizer exclusive global rights to develop and commercialize the oral GLP-1R agonist YP05002, with a total transaction value of up to $2.085 billion [1][3][4]. Group 1: Pfizer's Strategic Moves - Pfizer's recent acquisition of Metsera for over $10 billion and the licensing deal for YP05002 reflect its commitment to expanding its weight loss drug portfolio amid impending patent expirations for several key products [3][4]. - The company plans to invest $10-15 billion in mergers and acquisitions by 2025, indicating a proactive approach to filling revenue gaps caused by patent cliffs [3][4]. - Pfizer's recent transactions highlight its determination to capture a significant share of the weight loss market, which is projected to be worth hundreds of billions [3][4]. Group 2: Fosun Pharma's International Strategy - The collaboration with Pfizer is a significant milestone for Fosun Pharma, enhancing its internationalization strategy and accelerating the global development of YP05002 [2][10]. - Fosun Pharma has completed six external business development deals in 2025, totaling approximately $4 billion, which includes various innovative drug pipelines [10][11]. - The partnership with Pfizer not only boosts Fosun's revenue potential but also strengthens its core technology platforms in antibody, ADC, cell therapy, and small molecule innovation [10][11]. Group 3: Market Dynamics and Competitors - The weight loss drug market is experiencing a surge, with multiple companies reporting positive clinical data for their GLP-1 drugs, leading to significant stock price increases [5][6]. - Notable competitors include ShouTi Bio and EQRx, which have reported promising results for their respective GLP-1 drugs, indicating a competitive landscape [5][6]. - The emergence of next-generation weight loss drugs, including small molecules and siRNA therapies, suggests a dynamic and evolving market with various players vying for market share [8][9][14].
复星医药:子公司朝晖药业”酮洛芬贴剂“获临床试验批准
Ge Long Hui· 2025-12-12 12:06
Group 1 - The core point of the article is that Fosun Pharma's subsidiary, Shanghai Chaohui Pharmaceutical, has received approval from the National Medical Products Administration to conduct clinical trials for the drug Ketoprofen patch in China [1] - The drug is primarily intended for pain relief and anti-inflammatory treatment for conditions such as low back pain, osteoarthritis, shoulder periarthritis, tendonitis, and rheumatoid arthritis [1] - As of October 2025, the cumulative R&D investment for this drug by the group is approximately RMB 960,000 (unaudited) [1] Group 2 - According to IQVIA CHPA data, the sales revenue for Ketoprofen formulations in China is projected to be approximately RMB 91.16 million in 2024 [1]
复星医药(02196.HK):复宏汉霖”斯鲁利单抗注射液“药品注册申请获受理
Ge Long Hui· 2025-12-12 11:51
Core Viewpoint - Fosun Pharma's subsidiary, Shanghai Fuhong Hanlin Biotech, has received acceptance for a new indication application for its drug, Surulitinib Injection, from the National Medical Products Administration of China, which has been included in the priority review process [1] Group 1: Drug Development and Approvals - Surulitinib Injection is an innovative anti-PD-1 monoclonal antibody developed by the company [1] - The drug has been approved for marketing in multiple countries/regions, including China, the EU, the UK, Indonesia, Cambodia, Thailand, Malaysia, Singapore, and India [1] - Current approved indications in China include first-line treatment for squamous non-small cell lung cancer (sq-NSCLC), extensive-stage small cell lung cancer (ES-SCLC), esophageal squamous cell carcinoma (ESCC), and non-squamous non-small cell lung cancer (nsq-NSCLC) [1] Group 2: Regulatory Designations and Clinical Trials - The drug has received orphan drug designation from regulatory authorities in the US, EU, Switzerland, and South Korea [1] - The indication for gastric cancer in combination with chemotherapy has been included in the breakthrough therapy program by the National Medical Products Administration of China as of November 2025 [1] - Multiple combination therapies involving this drug are currently undergoing clinical trials in various countries and regions, targeting indications such as lung cancer, esophageal cancer, head and neck squamous cell carcinoma, colorectal cancer, and gastric cancer [1]
复星医药(02196.HK):子公司朝晖药业”酮洛芬贴剂“获临床试验批准
Ge Long Hui· 2025-12-12 11:45
Core Viewpoint - Fosun Pharma's subsidiary, Shanghai Chaohui Pharmaceutical, has received approval from the National Medical Products Administration to conduct clinical trials for the ketoprofen patch in China, indicating a significant step in the development of this pain relief medication [1] Group 1: Clinical Trial Approval - The ketoprofen patch is intended for clinical trials in China, specifically for Phase III trials once conditions are met [1] - The drug is a chemical medication primarily aimed at treating pain and inflammation associated with various conditions, including lower back pain, osteoarthritis, and rheumatoid arthritis [1] Group 2: Research and Development Investment - As of October 2025, the cumulative R&D investment for the ketoprofen patch by the group is approximately RMB 960,000 (unaudited) [1] - The projected sales revenue for ketoprofen formulations in China for 2024 is estimated to be around RMB 91.16 million [1]
复星医药(02196):酮洛芬贴剂获临床试验批准
智通财经网· 2025-12-12 11:42
Core Viewpoint - Fosun Pharma's subsidiary, Shanghai Chaohui Pharmaceutical Co., has received approval from the National Medical Products Administration to conduct clinical trials for Ketorolac patches, indicating a significant step in the development of this pain relief medication [1] Group 1: Clinical Trial Approval - The approval allows for the initiation of Phase III clinical trials for the Ketorolac patches in China once conditions are met [1] - The drug is classified as a chemical medication and is intended for pain relief and anti-inflammatory treatment for various conditions [1] Group 2: Indications for Use - The Ketorolac patches are primarily aimed at treating pain and inflammation associated with conditions such as lower back pain, osteoarthritis, shoulder periarthritis, tendonitis, and muscle pain [1] - Additionally, the patches are indicated for local pain relief in rheumatoid arthritis [1]
复星医药(02196) - 海外监管公告 - 关於控股子公司药品註册申请获受理的公告
2025-12-12 11:41
上 海 復 星 醫 藥( 集 團 )股 份 有 限 公 司 Shanghai Fosun Pharmaceutical (Group) Co., Ltd.* (於中華人民共和國註冊成立的股份有限公司) 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份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。 (股份代號:02196) 海外監管公告 本公告乃根據香港聯合交易所有限公司證券上市規則第13.10B條而作出。 上海復星醫藥(集團)股份有限公司 董事長 陳玉卿 中國,上海 2025 年1 2 月1 2 日 於本公告日期,本公司之執行董事為陳玉卿先生、關曉暉女士、文德鏞先生、王可心先生及劉毅先生; 本公 司之非執行董事為陳啟宇先生及潘東輝先生; 本公司之獨立非執行董事為余梓山先生、王全弟先生、Chen Penghui先生及楊玉成先生;以及本公司職工董事為嚴佳女士。 * 僅供識別 茲載列上海復星醫藥(集團)股份有限公司(「本公司」)在上海證券交易所網站刊登的《關於 控股子公司藥品註冊申請獲受理的公告》,僅供 ...
复星医药(02196) - 海外监管公告 - 关於控股子公司药品获临床试验批准的公告
2025-12-12 11:35
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份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。 (於中華人民共和國註冊成立的股份有限公司) (股份代號:02196) 海外監管公告 本公告乃根據香港聯合交易所有限公司證券上市規則第13.10B條而作出。 茲載列上海復星醫藥(集團)股份有限公司(「本公司」)在上海證券交易所網站刊登的《關於 控股子公司藥品獲臨床試驗批准的公告》,僅供參閱。 承董事會命 上海復星醫藥(集團)股份有限公司 上 海 復 星 醫 藥( 集 團 )股 份 有 限 公 司 Shanghai Fosun Pharmaceutical (Group) Co., Ltd.* 证券代码:600196 股票简称:复星医药 编号:临 2025-197 上海复星医药(集团)股份有限公司 关于控股子公司药品获临床试验批准的公告 董事長 陳玉卿 中國,上海 2025 年1 2 月1 2 日 於本公告日期,本公司之執行董事為陳玉卿先生、關曉暉女士、文德鏞先生、王可心先生及劉毅先生;本公 司之非執行董事 ...