Core Viewpoint - The collaboration between domestic biotech company InnoCare (诺诚健华) and US-based Zenas BioPharma is a significant licensing deal, valued at over $2 billion, aimed at advancing InnoCare's autoimmune pipeline products internationally, particularly the core product Obexelimab [1][8]. Group 1: Financial Aspects - The total deal value exceeds $2 billion, including an upfront payment and near-term payments totaling approximately $294 million, which consists of $100 million in cash and 7 million shares of Zenas stock valued at around $194 million [8][10]. - InnoCare is also entitled to receive additional milestone payments based on clinical development, registration, and commercialization achievements, with potential royalties on net sales reaching up to 19% [8][10]. Group 2: Strategic Rationale - InnoCare chose Zenas due to its strong alignment in the autoimmune disease space, particularly in multiple sclerosis, which complements the development of Obexelimab [3][4]. - Zenas's leadership, particularly CEO Lonnie Moulder, brings extensive experience in clinical development and commercialization, enhancing the potential for successful international product development [5][6]. - The collaboration is seen as a strong partnership that could significantly increase the chances of success for Obexelimab in global Phase III clinical trials and expand its application to more autoimmune indications [4][5]. Group 3: Market Reception - Analysts from Goldman Sachs have maintained a "Buy" rating for InnoCare, raising the price targets for its Hong Kong and A-shares by 21.7% and 54.6%, respectively, indicating strong market confidence in the deal [2][1]. - Zenas has received a "Strong Buy" rating from Wall Street analysts, with an average target price of $33.25, reflecting positive sentiment regarding its potential in the autoimmune sector [6][7]. Group 4: Industry Impact - This licensing agreement sets a new record for external licensing in China's autoimmune sector, showcasing InnoCare's ability to attract international partnerships and recognition for its innovative drug pipeline [8][12]. - The successful international collaboration is viewed as a testament to the growing strength of Chinese biotech firms in the global market, enhancing confidence in the internationalization of China's biopharmaceutical industry [12].

Core Viewpoint - The recent licensing agreement between Nuo Cheng Jian Hua and Zenas has led to a significant market reaction, with Nuo Cheng Jian Hua's stock dropping while Zenas's stock surged, indicating a divergence in market sentiment regarding the deal's value and potential [1][2]. Summary by Sections Licensing Agreement Details - Nuo Cheng Jian Hua has licensed its BTK inhibitor, Oubutini, for multiple sclerosis and other autoimmune diseases to Zenas, receiving an upfront payment of $100 million, milestone payments, and 7 million shares of Zenas stock, with a total potential deal value exceeding $2 billion [1][2]. - The upfront payment and stock value combined amount to $280 million, which is considered reasonable compared to industry standards, where the average upfront payment ratio is around 8% [3]. Market Reaction and Sentiment - The market's cautious sentiment towards the deal stems from two main concerns: the upfront payment not meeting expectations and the perceived lack of recognition of Zenas as a partner [2][5]. - Nuo Cheng Jian Hua's stock fell by 6.24% in A-shares and 11.64% in Hong Kong shares, while Zenas's stock rose by 24.22% following the announcement [1]. Strategic Considerations - Nuo Cheng Jian Hua had previously engaged with multinational corporations (MNCs) but ultimately chose Zenas due to smoother communication and Zenas's strong clinical development capabilities, particularly in the field of multiple sclerosis [5][10]. - Zenas, founded in 2019 and listed on NASDAQ in 2024, currently has no commercial products but has a promising pipeline, including a dual-function monoclonal antibody that complements Oubutini [7][8]. Industry Context - The collaboration reflects a shift in the global innovation drug landscape from one-time licensing deals to deeper collaborative models, where local pharmaceutical companies can retain equity in new ventures [12]. - Nuo Cheng Jian Hua's previous partnership with Biogen ended after about 18 months, highlighting the challenges in securing long-term collaborations in the industry [11]. Future Outlook - The partnership aims to advance the development of Oubutini in treating primary and secondary progressive multiple sclerosis, with significant market opportunities projected in the U.S. alone [8]. - The success of this collaboration will depend on Zenas's ability to progress its pipeline and the overall market performance of its shares [12].

Core Viewpoint - The domestic innovative drug company, Nuo Cheng Jian Hua, has re-entered the international market with its BTK inhibitor, Obexelimab, through a licensing agreement with Nasdaq-listed Zenas, with a total transaction value exceeding $2 billion [1][2]. Group 1: Licensing Agreement Details - Nuo Cheng Jian Hua has signed a licensing agreement with Zenas, granting exclusive global rights for Obexelimab in multiple sclerosis (MS) and other indications outside Greater China and Southeast Asia [1]. - The agreement includes an upfront payment of $100 million and milestone payments, along with 7 million shares of common stock from Zenas, representing approximately 9.3% of Zenas' issued and outstanding shares [1][2]. - Zenas plans to initiate a Phase 3 study for secondary progressive MS (SPMS) in Q1 2026 and advance the IL-17 and TYK2 inhibitors into clinical stages in 2026 [2]. Group 2: Market Potential and Product Pipeline - The commercial opportunity for SPMS and primary progressive MS (PPMS) in the U.S. is estimated to exceed $12 billion, with SPMS and PPMS accounting for 20% and 10-15% of all MS subtypes, respectively [4]. - Obexelimab is a key product for Nuo Cheng Jian Hua, which has already been approved in China for various hematological malignancies since December 2020 [3][4]. Group 3: Strategic Considerations - Nuo Cheng Jian Hua's choice of Zenas as a partner was influenced by Zenas' clinical development capabilities in the autoimmune field and the successful entrepreneurial background of Zenas' founder, Lonnie Moulder [5][6]. - The collaboration is expected to facilitate the rapid advancement of Obexelimab and other products into international markets, leveraging Zenas' resources and influence [6][7]. Group 4: Financial Performance - In the first half of 2025, Nuo Cheng Jian Hua reported revenue of 731 million yuan, a year-on-year increase of 74.26%, with Obexelimab sales reaching 637 million yuan, up 52.84% [8]. - The company had a cash and cash equivalents balance of 4.701 billion yuan as of mid-2025 [9].

截至2025年10月9日 13:04，恒生港股通创新药精选指数下跌4.58%。成分股方面涨跌互现，石四药集团领涨3.12%，华润医药上涨1.23%，山东新华制药股份 上涨0.99%；诺诚健华领跌9.73%，荣昌生物下跌9.36%，科伦博泰生物-B下跌8.31%。港股创新药精选ETF(520690)下跌0.49%，最新报价1.02元。拉长时间 看，截至2025年9月30日，港股创新药精选ETF近2周累计上涨1.09%。 流动性方面，港股创新药精选ETF盘中换手19.17%，成交8400.15万元，市场交投活跃。拉长时间看，截至9月30日，港股创新药精选ETF近1月日均成交1.58 亿元。 截至2025年10月9日 13:03，恒生医疗保健指数下跌3.31%。成分股方面涨跌互现，脑动极光-B领涨7.79%，心泰医疗上涨3.52%，同仁堂国药上涨3.37%；诺 诚健华领跌9.78%，科伦博泰生物-B下跌8.23%，四环医药下跌7.69%。恒生医疗ETF(513060)上涨0.14%， 冲击3连涨。最新价报0.74元。拉长时间看，截至 2025年9月30日，恒生医疗ETF近2周累计上涨1.24%。 流动性方面，恒生医 ...

Core Viewpoint - The company announced a licensing agreement with Zenas for its core product, Orelabrutinib, in the field of multiple sclerosis and other non-oncological treatments, while retaining rights in oncology [1][2]. Group 1: Licensing Agreement Details - The agreement includes a $100 million upfront payment and potential milestone payments, with a total deal value exceeding $2 billion [1]. - Zenas will also issue 7 million shares of common stock to the company, with additional payments tied to clinical development and commercialization milestones [1]. - The agreement allows Zenas to develop and commercialize Orelabrutinib globally for multiple sclerosis and other non-cancer indications [1][2]. Group 2: Product and Market Insights - Orelabrutinib is currently approved for three indications in hematological cancers in China, with ongoing clinical trials for multiple sclerosis [2]. - The company retains exclusive global rights for Orelabrutinib in oncology, establishing a dual strategy of self-research in oncology and licensing in autoimmune diseases [2]. - The new oral IL-17 AA/AF inhibitor and the brain-penetrant oral TYK2 inhibitor are in preclinical stages, targeting autoimmune diseases like psoriasis and psoriatic arthritis [3]. Group 3: Market Context and Future Prospects - The global market for multiple sclerosis treatments is significant, particularly in Europe and North America, where the disease has a higher prevalence [5]. - The company’s Orelabrutinib shows advantages in kinase selectivity and binding affinity, indicating strong clinical development potential [5]. - The oral IL-17 AA/AF inhibitor addresses the challenge of injection-based therapies, which may improve patient compliance [5]. Group 4: Financial Position - As of June 30, 2025, the company holds approximately 7.68 billion yuan in cash and equivalents, indicating a strong financial position within the biotech sector [6].

潜在交易额超20亿美元 诺诚健华达成重磅对外授权协议 ◎记者 张雪 奥布替尼被寄予厚望 潜在总交易金额超20亿美元 诺诚健华将获得1亿美元的首付款及近期里程碑付款，以及Zenas发行的700万股普通股。未来，诺诚健 华还有权获得潜在的研发及注册里程碑付款、商业化里程碑付款，并从授权产品的年度净销售额中收取 最高达百分之十几的特许权使用费，总交易金额或将超过20亿美元。 奥布替尼是全球首个进入Ⅲ期临床的中枢神经系统强渗透性BTK抑制剂，针对原发进展型多发性硬化症 （PPMS）的全球Ⅲ期试验已于2025年三季度启动，预计2026年一季度启动继发进展型（SPMS）试 验。此前Ⅱ期数据显示，其显著减少脑部炎症病灶，且安全性优异。 通过此次合作，Zenas将获得奥布替尼在多发性硬化领域的全球独家开发、生产和商业化权利，以及奥 布替尼在非肿瘤领域除大中华区及东南亚地区以外区域的权利。Zenas还将获得口服IL-17AA/AF抑制剂 除大中华区及东南亚地区外的独家开发、生产和商业化权利，以及透脑性口服TYK2抑制剂的全球权 利。"我们预计2026年将这两款抑制剂推向临床，并预计2027年获得口服IL-17AA/AF抑制剂的 ...

Core Insights - The collaboration between Nocera Biopharma and Zenas BioPharma involves a global licensing agreement worth over $2 billion, focusing on the development of Orelabrutinib for multiple sclerosis and other autoimmune diseases [2][4]. Group 1: Agreement Details - Zenas will receive global exclusive rights for Orelabrutinib in the multiple sclerosis field and rights for non-oncology development and commercialization outside Greater China and Southeast Asia [4][5]. - Nocera Biopharma will receive an upfront payment of $100 million, milestone payments, and 7 million shares of common stock from Zenas, along with royalties of up to a percentage of annual net sales from licensed products [4][6]. Group 2: Product Potential - Orelabrutinib is the first highly permeable BTK inhibitor for the central nervous system to enter Phase III clinical trials, with trials for primary progressive multiple sclerosis (PPMS) starting in Q3 2025 and secondary progressive multiple sclerosis (SPMS) trials expected to begin in Q1 2026 [4][8]. - The drug has shown significant efficacy in reducing brain inflammation and has an excellent safety profile based on Phase II data [4][8]. Group 3: Strategic Focus - Nocera Biopharma retains global rights for Orelabrutinib in oncology and non-oncology rights in Greater China and Southeast Asia, indicating a strategic focus on dual therapeutic areas [6][8]. - The company aims to enhance its drug discovery platform to develop first-in-class and best-in-class therapies for autoimmune diseases, addressing unmet medical needs in China and globally [9].

Core Viewpoint - Sichuan Baili Tianheng Pharmaceutical Co., Ltd. has re-submitted its listing application to the Hong Kong Stock Exchange, marking the third attempt since last year [1]. Company Overview - Baili Tianheng completed a private placement in A-shares, raising a total of 3.764 billion yuan, with funds allocated entirely for innovative drug research and development [3]. - The company primarily operates in the innovative biopharmaceutical sector and traditional Chinese medicine, with key products including Propofol emulsion injection [5]. - As of September 30, the company's market capitalization reached 155 billion yuan, with its chairman, Zhu Yi, holding 72.22% of the shares, valued at approximately 112.853 billion yuan [6]. Financial Performance - The company reported significant financial fluctuations, with revenues of 703 million yuan in 2022, declining to 562 million yuan in 2023, and projected to rise to 5.823 billion yuan in 2024. However, net profits showed a loss of 282 million yuan in 2022, escalating to a loss of 1.12 billion yuan in the first half of 2025 [6]. - For the first half of 2025, the company recorded revenues of 171 million yuan, a 96.9% decrease year-on-year, and a net loss of 1.12 billion yuan, a 124% decline compared to the previous year [7]. - R&D expenses accounted for 606.69% of revenue in the first half of 2025, reflecting a significant increase in investment in innovation [8]. Industry Context - There is a growing trend among A-share pharmaceutical companies to pursue dual listings in Hong Kong, with at least 10 companies announcing progress on "A+H" plans this year [10]. - The Hong Kong market has seen a resurgence in biotech listings, with 10 biotech companies listed under Chapter 18A of the Main Board Listing Rules, raising approximately 8.05 billion HKD [11]. - The innovative drug sector has gained traction, with the Wind Innovation Drug Index rising by 51.22% year-to-date, indicating a robust market environment for pharmaceutical investments [12].

Group 1 - The core idea is that companies with a global market reach, like those in the US, achieve higher valuations compared to local companies that primarily sell domestically [1][3] - Companies that sell products internationally have a significantly larger revenue potential, as they can tap into billions of potential customers across various regions [3] - The article highlights that many Chinese companies are still confined to local markets, facing intense competition and low profit margins, which limits their valuations [3] Group 2 - The pharmaceutical industry, particularly innovative drug companies, is positioned to become a major wealth generator as successful drugs can be sold at high prices globally [5] - Chinese biotech firms are increasingly gaining recognition on the international stage by licensing their innovative drugs to global companies, leading to substantial revenue contracts [5] - Once these companies establish a foothold overseas, their valuation shifts from being seen as local players to global healthcare competitors, attracting significant capital investment [7] Group 3 - The potential for future pharmaceutical giants in A-shares and Hong Kong stocks is high, with expectations that companies exceeding valuations of 100 billion or even 300 billion will emerge from this group of "outbound pioneers" [7] - Investing in innovative drugs carries risks, including research failures and regulatory hurdles, necessitating careful analysis to distinguish between genuinely promising companies and those that may not deliver [7] - The future winners in the market will be those companies that are willing to expand globally and generate revenue from international markets, with innovative drugs being a key avenue for Chinese firms to achieve this [7]

Group 1 - Pharmaceutical stocks are experiencing a strong rally, with notable increases in share prices for companies such as Clover Biopharmaceuticals (up 20.26%), Genscript Biotech (up 15.05%), and others [1] - On September 26, former President Trump announced a 100% tariff on any brand or patented pharmaceutical products starting October 1, 2025, unless companies establish manufacturing facilities in the U.S. [1] - Southwest Securities predicts uncertainty regarding the implementation of this executive order, suggesting that Chinese innovative drug companies heavily reliant on the U.S. market may face short-term pressure [1] - China’s innovative drug companies that engage in business development (BD) overseas are expected to be less affected, particularly those involved in license-out agreements, which are essentially intellectual property transactions [1] - China Post Securities believes the actual impact of the tariffs will be minimal, viewing the current price drop as a good opportunity to increase holdings in innovative drugs [1] Group 2 - From the perspective of catalysts in the innovative drug sector, October will see significant industry conferences such as ESMO (October 17-21), followed by ASH and the San Antonio Breast Cancer Symposium in December [2] - There has been ongoing progress in outbound licensing transactions this year, with several significant deals already completed, indicating potential opportunities for high-quality domestic innovative drugs to enter international markets [2] - The fourth quarter is expected to bring domestic policy implementations, including adjustments to the medical insurance catalog [2]