Investment Rating - The report maintains an "Accumulate" rating for the pharmaceutical and biotechnology sector [8] Core Insights - The report highlights that the pharmaceutical sector, particularly the innovative drug segment, is experiencing a significant bull market, with the innovation drug index outperforming other indices [2][13] - The report emphasizes the strong liquidity in the market, which has led to increased investment in innovative drugs, particularly those related to PD1 and weight loss drugs [2][15] - Future outlook remains optimistic for 2025, focusing on innovative drugs, new technologies, and restructuring of the supply chain [3][16] Summary by Sections 1. Pharmaceutical Core Insights - The pharmaceutical index increased by 1.40% during the week of June 9-13, outperforming both the ChiNext and CSI 300 indices [13] - The innovative drug index rose by 3.07%, indicating strong market performance [50] 2. MNC Cash and Potential Layouts - MNCs have substantial cash reserves, with major companies like Johnson & Johnson and Merck holding over $10 billion in cash, indicating strong purchasing power for potential business development (BD) opportunities [27][25] - The report analyzes MNC revenue sources, highlighting a focus on oncology, metabolism, and mental health, which are areas of high market potential [25][27] 3. Investment Strategies and Thoughts 3.1 Broad Pharmaceuticals - Innovative drugs are a key focus, with a recommendation to explore opportunities in core stocks and those with BD expectations [3][16] - The report identifies specific companies for investment, including major players in the innovative drug space and smaller market cap stocks with promising pipelines [17][18] 3.2 Generic Drugs - The generic drug sector showed a weekly increase of 5.24%, outperforming the broader pharmaceutical index [59] - Top-performing stocks in the generic sector include Yiming Pharmaceutical and Sai Sheng Pharmaceutical, indicating strong market activity [62] 4. Market Review and Hotspot Tracking - The report notes that innovative drugs are becoming the most attractive sector, with significant price increases observed in several companies due to market catalysts [2][15] - Key events, such as the NMPA's inclusion of a new treatment for cardiovascular disease, are highlighted as important developments in the sector [57]

Group 1 - In May, new RMB deposits exceeded 2 trillion, while new RMB loans were nearly 620 billion, indicating a disparity in growth between deposits and loans due to changes in financial institutions' asset diversification and financing structures [1] - The "Guzi economy" has rapidly exploded, with the Taotian toy industry achieving a market share of 70% during the first phase of the 618 shopping festival, significantly surpassing last year's performance [1] - Micron has confirmed the discontinuation of DDR4 production, with expectations of severe shortages in the coming quarters, particularly affecting the PC and data center sectors [1] Group 2 - The search volume for "LABUBU" on the Xianyu platform surged by 1000% month-over-month, indicating a strong demand for rental services of LABUBU figurines [2] - Multiple counterfeit LABUBU factories in Dongguan have ceased operations, likely due to increased copyright enforcement [2] - Minsheng Securities' chief strategist, Miao Yiling, has left the company, marking a significant change in the firm's research leadership [3] Group 3 - China Pacific Insurance reported a total premium income of 227.169 billion for its two subsidiaries in the first five months, with a year-on-year growth of 10.2% for life insurance [6] - Goldway plans to repurchase shares worth between 100 million to 150 million, with a maximum repurchase price set at 53 yuan per share [11] - Nanjing Julong intends to invest 130 million in a new production project for special materials, aiming for an annual output of 40,000 tons [10] Group 4 - A strategic research collaboration between Stone Pharmaceutical Group and AstraZeneca has been established, with potential earnings exceeding 5 billion from milestone payments and royalties [7] - The China Securities Regulatory Commission has approved the registration application for Jiangxi Aifenda's IPO on the Growth Enterprise Market [6] - Xizi Elevator has appointed Gao Feng as the new chairman following the passing of the previous chairman [4][5]

Core Insights - AstraZeneca has entered into a strategic research collaboration with CSPC Pharmaceutical Group to advance the discovery and development of new oral candidate drugs targeting high-priority indications [1] Financial Terms - CSPC will receive an upfront payment of $110 million and is eligible for up to $1.62 billion in potential research milestone payments and up to $3.6 billion in potential sales milestone payments [1] - Additionally, CSPC may receive single-digit sales royalties based on the annual net sales of the relevant products [1] Development Rights - AstraZeneca retains the option to obtain exclusive rights for the global development and commercialization of the candidate drugs [1]

本文节选自彭博终端。如您还不是终端用户，您可在文末" 阅读原文 "联系我们预约产品演示。 彭博行业研究 2025 ASCO年会报告 近期，2025年美国临床肿瘤学会（ASCO）年会在美国芝加哥举办。阿斯利康连续第七年成为 大会领头羊，展示了对实践具有变革意义的数据，有望助力其在 2030 年实现 800 亿美元销售 额的目标。今年的重点主要集中在胃癌领域：英飞凡（Imfinzi）的 MATTERHORN 研究凭借 前所未有的无事件生存期（EFS）优势，打开了一个 20 亿美元的市场；以及乳腺癌领域：优 赫得（Enhertu）在一线 HER2 阳性乳腺癌的 DESTINY-Breast09 试验中再次发力。 包括TIGIT和KRAS在内的多种肺癌数据集正在新的利基领域取得进展，而在其他领域，辉瑞 的Braftovi使结直肠癌患者的总生存期（OS）增加了一倍。在经历了20年的停滞之后，Bristol Myers的Opdivo和默克的Keytruda终于在头颈癌领域取得了进展。 长按或扫描二维码 阅读完整报告 * 本报告语言为英文。 凭借KEYNOTE-585试验，阿斯利康抓住了默克公司在胃癌围手术期中错失的机会。 ...

Core Viewpoint - Goldman Sachs provided key insights on AstraZeneca at its 46th Global Healthcare Conference, highlighting the company's management's reaffirmation of limited impact from potential drug tariffs and a clearer path to achieving $80 billion in revenue by 2030, alongside a target operating profit margin of around 35% [1] Group 1: Financial Outlook - AstraZeneca aims for an operating profit margin of approximately 35% while acknowledging uncertainties such as the inclusion of Farxiga in China's volume-based procurement in late 2025 and potential price reductions in the U.S. due to the Inflation Reduction Act (IRA) [2] - The company expects revenue growth and cost control to jointly drive profit margin improvements, with a projected impact of a few percentage points on total revenue from the redesign of the Medicare Part D program in 2025 [2] - Goldman Sachs maintains a "Buy" rating on AstraZeneca with a 12-month price target of $97, indicating nearly a 33% upside from the stock's closing price on June 9 [1] Group 2: Drug Development and Pipeline - AstraZeneca is optimistic about the Phase 3 trial of baxdrostat, learning from previous Phase 2 trials, and expects peak sales of $5 billion, with half from monotherapy and half from combination therapy with dapagliflozin [3] - The company emphasizes the importance of initiating cardiovascular, renal, and metabolic disease (CVRM) drug trials early to gather sufficient data for reimbursement purposes, despite these trials not being required for regulatory approval [3] - AstraZeneca is confident in the prospects of Enhertu for first-line treatment in HER2-positive breast cancer, reporting about a 50% complete response rate in metastatic patients [4] Group 3: Regulatory and Market Considerations - AstraZeneca's management noted uncertainties regarding the implementation of Most Favored Nation clauses and the IRA's role in lowering drug prices, while supporting increased healthcare budgets in European countries to foster innovation [2] - The company is increasing its investment in biologics while continuing to invest in small molecule drugs, such as oral GLP-1 and PCSK9 inhibitors [2] - AstraZeneca does not foresee ESR1 mutation testing as a barrier to the promotion of camizestrant, citing several operational advantages and prior experience with BRCA testing [3]

的术后辅助患者可能受商保影响。此外，不同地区参保率差异显著，发达地区 如广东、上海参保率较高，而落后地区参保率低。因此，总体而言，商保政策 对这些药品的市场覆盖不会产生重大变化。 弘则医享汇｜创新药大品种跟踪 - 三代 TKI 市场的商业化 趋势 20250610 摘要 反腐政策对部分外资药企（如阿斯利康）的推广活动产生限制，会议覆 盖率显著下降，对其销售增长构成一定挑战。但对已纳入医保的三代 TKI 产品影响较小，商保影响主要集中在术后辅助治疗患者。 奥希替尼 2025 年全年增长目标已下调至 10%左右，上半年增长仅 4%，且在压货情况下仍微跌，实现双位数增长面临挑战。公司政策对市 场推广的严格限制是主要阻碍。 EGFR 和 c-MET 双抗产品市场前景取决于基因检测技术的普及与提升。 c-MET 靶点联合用药（如与 ADC 联合）在耐药基因治疗中具有潜力， 市场容量或可达 10 亿级别，但需等待临床数据验证。 国产第三代 TKI 产品陆续上市，但市场份额主要由艾克替尼、贝福替尼、 瑞尔替尼占据，新产品难以撼动现有格局，除非进行大规模资源投入。 国家反腐政策限制了大规模投入的可能性。 阿斯利康侧重 TOP ...

Core Insights - The FDA approved Merck's Enflonsia to protect infants from respiratory syncytial virus (RSV), competing with Sanofi and AstraZeneca's Beyfortus [1][4] - Merck plans to launch Enflonsia ahead of the RSV season, with orders expected to start in July [2] - The approval provides a new treatment option for RSV, which causes significant mortality and hospitalization among infants [3] Company Developments - Merck aims to ensure availability of Enflonsia in the U.S. before the RSV season to alleviate the burden on families and healthcare systems [4] - Enflonsia is a preventative monoclonal antibody that can be administered to infants regardless of weight, offering dosing convenience [5] - Sanofi is increasing the supply of Beyfortus, which generated €1.7 billion ($1.8 billion) in sales last year [6] Industry Context - Other companies, including Pfizer, GSK, and Moderna, offer RSV vaccines, but these are limited to adults and pregnant women [6] - A meeting of CDC vaccine advisors is scheduled for June 25 to 27 to discuss recommendations for RSV shots and other immunizations [7] - In clinical trials, Enflonsia reduced RSV-related hospitalizations by over 84% and lower respiratory infections requiring medical attention by more than 60% compared to a placebo [8]

"乳腺癌治疗正朝着更精准的分型和机制，不断推出多种创新治疗方案。创新药物的突破只是起点，要 真正惠及患者，还需要解决教育、可及和指南指导规范化实践之间的衔接问题。"阿斯利康中国肿瘤业 务总经理关冬梅在接受新华网采访时表示。 阿斯利康中国肿瘤业务总经理 关冬梅 在2025年美国临床肿瘤学会（ASCO）上，阿斯利康创连续七年亮相全体大会（Plenary Session）记 录。其在乳腺癌领域发布的两项重磅研究成果——SERENA-6与DESTINY-Breast09，聚焦于HR阳 性/HER2阴性和HER2阳性这两个乳腺癌的重要分子亚型，展现了其在精准诊疗探索上的持续深耕。 在关冬梅看来，在中国乳腺癌患者人数持续攀升的背景下，更值得思考的是："如何把这些研究转化为 切实可行的诊疗实践，真正改变患者结局。" 三大分子分型协同推进，精准布局覆盖治疗全周期 在乳腺癌不同分型精准治疗持续深化的背景下，阿斯利康围绕HER2阳性、HR阳性/HER2阴性、三阴性 三大乳腺癌分子分型中构建了完整的治疗方案体系。"已上市产品和临床管线覆盖了从早期到晚期的各 个治疗阶段，包含新辅助、辅助、晚期一线、一线进展后全周期的精准靶向药物，我 ...

小细胞肺癌是一种高侵袭性的肺癌类型。尽管局限期小细胞肺癌患者对初始化疗和放疗有应答，但仍会 复发并且进展迅速。局限期小细胞肺癌患者预后极差，只有15%～30%的患者在确诊后可活过5年。 阿斯利康今日宣布，英飞凡®（通用名：度伐利尤单抗）已获中国国家药品监督管理局批准，作为单药 用于在接受铂类药物为基础的放化疗后未出现疾病进展的局限期小细胞肺癌成人患者的治疗。据悉，此 次获批是基于ADRIATIC Ⅲ期临床试验的积极结果。结果显示，与安慰剂相比，度伐利尤单抗可降低死 亡风险27%。 中国抗癌协会小细胞肺癌专委会主任委员、ADRIATIC临床研究的全球指导委员会委员及中国主要研究 者程颖教授表示："此次获批标志着度伐利尤单抗成为数十年来首个且唯一治疗局限期小细胞肺癌的免 疫治疗方案，这将为中国的该类患者带来更多的治疗选择。ADRIATIC试验中，接受度伐利尤单抗治疗 的患者显示出了显著的总生存获益，三年总生存率高达57%，度伐利尤单抗有望成为中国乃至全球的治 疗新标准。" 阿斯利康中国肿瘤业务总经理关冬梅表示："此次获批不仅有望革新局限期小细胞肺癌的治疗格局，更 重要的是将助力全期别小细胞肺癌患者改善其预后。" ...

此次获批是基于ADRIATIC Ⅲ期临床试验的积极结果。此前，ADRIATIC全球临床试验的数据成功发表 于全球四大顶级医学期刊之一《新英格兰医学杂志》（NEJM）；其中国队列研究数据的结果已于今年 在欧洲肺癌大会（ELCC）上公布。 ADRIATIC试验中，接受度伐利尤单抗治疗的患者显示出了显著的总生存获益，三年总生存率高达 57%。度伐利尤单抗单药治疗组的中位无进展生存期为16.6个月，而安慰剂组为9.2个月。估计接受度伐 利尤单抗治疗的患者中有46%在两年时未出现疾病进展，而安慰剂组为34%。此外，ADRIATIC中国队 列研究数据显示，中国患者群体的总生存期（OS）与无进展生存期（PFS）获益结果与全球研究的总体 结果一致，表明与安慰剂相比，度伐利尤单抗可将死亡风险降低29%，将疾病进展或死亡风险降低 33%。 小细胞肺癌是一种高侵袭性的肺癌类型。在中国，每年大约有34000名局限期小细胞肺癌（LS-SCLC， Ⅰ-Ⅲ期）患者正在接受治疗。尽管局限期小细胞肺癌患者对初始化疗和放疗有应答，但仍会复发并且 进展迅速。局限期小细胞肺癌患者预后极差，只有15%-30%的患者在确诊后可活过5年。 新京报讯（记者 ...