Investment Rating - The report assigns a "Buy" rating for Jiangsu Hengrui Pharmaceuticals with a target price of Rmb123.000, indicating an expected share price return of 95.5% and an expected total return of 95.9% [4]. Core Insights - Jiangsu Hengrui Pharmaceuticals is positioned as a leading global biopharma, ranking No.2 in the size of its originated pipeline and No.3 in pipeline growth, benefiting from China's status as a significant source of global innovation [4][6]. - The report highlights that approximately 30% of global innovative drug trials originate from China, and about one-third of global innovative pipelines are from China-headquartered companies, indicating a robust growth trajectory for the industry [2][3]. - The Chinese pharmaceutical market shows significant potential for growth in innovative drugs, which currently account for only about 14% of total drug sales in hospitals, compared to much higher percentages in developed markets [3]. Summary by Sections Globalization and Innovation - Jiangsu Hengrui has made substantial progress in globalization, with over 20 global trials ongoing and a diversified portfolio across key therapeutic areas [6]. - The company leverages global partnerships and in-house capabilities to maximize innovation impact, with a strong record in out-licensing and strategic partnerships since 2018 [6]. Market Dynamics - The report notes that the demand for affordable innovation from China is expected to thrive due to increasing pricing pressures and the loss of exclusivity for leading multinational corporations [2]. - China's commitment to supporting innovative drugs is underscored by strong government backing for commercial health insurance, which is anticipated to improve coverage for innovative drugs in the future [3]. Financial Valuation - A discounted cash flow (DCF) approach is used to assess the fair value of Jiangsu Hengrui Pharmaceuticals, with a terminal growth rate of 4% and a weighted average cost of capital (WACC) of 8.3% [7].

Core Viewpoint - 恒瑞医药 has received approval from the National Medical Products Administration for multiple clinical trial applications for new drug candidates, indicating a significant advancement in its oncology pipeline [1][2][3][4][5] Group 1: New Drug Approvals - The company has received clinical trial approval for SHR-9839, a humanized antibody drug targeting advanced solid tumors, with a cumulative R&D investment of approximately 72.31 million [1] - SHR-A2009, an antibody-drug conjugate targeting HER3, has a cumulative R&D investment of about 227 million [2] - SHR-1826, targeting c-MET, has a cumulative R&D investment of around 101 million [2] - HRS-4642, a KRAS G12D inhibitor, has a cumulative R&D investment of approximately 191 million [2] - 阿得贝利单抗, a humanized anti-PD-L1 monoclonal antibody, has been approved for use in extensive-stage small cell lung cancer, with a cumulative R&D investment of about 969 million [3] - 注射用瑞康曲妥珠单抗, targeting HER2, has been approved for use in non-small cell lung cancer, with a cumulative R&D investment of around 1.415 billion [4] - SHR-A2102, an ADC targeting Nectin-4, has a cumulative R&D investment of approximately 248 million [5] - HRS-7058, a selective small molecule inhibitor for KRAS G12C mutations, has a cumulative R&D investment of about 69.57 million [5] Group 2: Market Context and Competitors - SHR-9839 is the only drug in its class currently in development, with one similar drug already approved globally [1] - SHR-A2009 is the first of its kind, with no similar drugs approved globally [2] - SHR-1826 has a competitor, ABBV399, which received accelerated approval in the U.S. for specific lung cancer patients [2] - 阿得贝利单抗 has several competitors, including Atezolizumab and Durvalumab, which collectively generated approximately 9.648 billion in global sales in 2024 [3] - 注射用瑞康曲妥珠单抗 has competitors like Ado-trastuzumab emtansine and Fam-trastuzumab deruxtecan, with a combined global sales forecast of about 6.557 billion in 2024 [4] - SHR-A2102 has one competitor, Enfortumab vedotin, with a projected global sales of approximately 1.949 billion in 2024 [5] - HRS-7058 faces competition from Sotorasib and Adagrasib, which are expected to generate around 485 million in global sales in 2024 [5]

Core Viewpoint - 恒瑞医药 and its subsidiaries have received approval from the National Medical Products Administration for multiple clinical trials of new drug candidates, indicating a strong pipeline and ongoing investment in innovative therapies [1] Group 1: Clinical Trial Approvals - The company has received approval for clinical trials for several drugs, including SHR-9839, SHR-A2009, SHR-1826, HRS-4642, and others [1] - SHR-9839 is a humanized antibody drug aimed at treating advanced solid tumors, with a cumulative R&D investment of approximately 72.31 million yuan [1] - SHR-A2009 is a HER3-targeted antibody-drug conjugate, with no similar drugs approved globally, and a cumulative R&D investment of about 227 million yuan [1] Group 2: Market Potential and R&D Investments - SHR-1826 is a c-MET-targeted antibody-drug conjugate, with a cumulative R&D investment of around 101 million yuan [1] - HRS-4642 is a KRASG12D inhibitor, with a cumulative R&D investment of approximately 191 million yuan [1] - The approved drug, 阿得贝利单抗, is indicated for first-line treatment of extensive-stage small cell lung cancer, with a projected global sales of similar products totaling about 9.648 billion USD in 2024 and a cumulative R&D investment of approximately 969 million yuan [1] Group 3: Future Drug Approvals and Sales Projections - 注射用瑞康曲妥珠单抗 is expected to be approved in China by May 2025 for HER2-mutant non-small cell lung cancer, with projected global sales of similar products totaling around 6.557 billion USD in 2024 and a cumulative R&D investment of about 1.415 billion yuan [1] - SHR-A2102 is a Nectin-4-targeted antibody-drug conjugate, with projected global sales of about 1.949 billion USD in 2024 and a cumulative R&D investment of approximately 248 million yuan [1] - HRS-7058 is a KRASG12C inhibitor, with projected global sales of similar products totaling around 485 million USD in 2024 and a cumulative R&D investment of about 69.57 million yuan [1]

Core Viewpoint - Heng Rui Medicine (01276) announced a share repurchase plan, indicating a strategic move to enhance shareholder value through stock buybacks [1] Summary by Relevant Sections Share Repurchase Details - In November 2025, the company repurchased 979,900 shares through the Shanghai Stock Exchange, representing 0.015% of the total share capital, with a maximum purchase price of RMB 63.28 per share and a minimum of RMB 59.32 per share, totaling RMB 59.7885 million (excluding transaction fees) [1] - As of November 21, 2025, the cumulative shares repurchased amounted to 8,898,700, accounting for 0.13% of the total share capital, with a maximum price of RMB 70.00 per share and a minimum of RMB 59.32 per share, totaling RMB 595 million (excluding transaction fees) [1]

Core Viewpoint - Morgan Stanley increased its stake in Heng Rui Medicine (01276) by purchasing 1,386,751 shares at an average price of HKD 71.5162 per share, totaling approximately HKD 9,917.52 million, raising its total holdings to about 16,748,500 shares, which represents a 6.48% ownership stake [1] Summary by Category - **Investment Activity** - Morgan Stanley's recent purchase of 1,386,751 shares indicates a strategic move to bolster its investment in Heng Rui Medicine [1] - The average purchase price of HKD 71.5162 per share reflects the firm's confidence in the company's future performance [1] - **Ownership Structure** - Following the acquisition, Morgan Stanley's total shareholding in Heng Rui Medicine increased to approximately 16,748,500 shares [1] - The updated ownership percentage of 6.48% signifies a notable presence in the company's shareholder base [1]

Core Viewpoint - Heng Rui Medicine has received approval from the National Medical Products Administration for multiple clinical trial applications, indicating a significant step forward in its drug development pipeline [1] Group 1: Clinical Trial Approvals - Jiangsu Heng Rui Medicine Co., Ltd. and its subsidiaries have been granted clinical trial approval for several injectable drugs, including SHR-9839(sc), SHR-A2009, SHR-1826, HRS-4642, and others [1] - The approval is based on compliance with the Drug Administration Law of the People's Republic of China, confirming that the drugs meet the necessary registration requirements [1] - The specific study includes an IB/II phase trial for SHR-9839(sc) in combination with anti-tumor drugs, focusing on safety, tolerability, and efficacy in solid tumor patients [1]

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所產生或因依賴 該等內容而引致的任何損失承擔任何責任。 Jiangsu Hengrui Pharmaceuticals Co., Ltd. 江蘇恒瑞醫藥股份有限公司 （於中華人民共和國註冊成立的股份有限公司） （股份代號：1276） 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條刊發。 根據中華人民共和國的有關法例規定，江蘇恒瑞醫藥股份有限公司（「本公司」）在 上海證券交易所網站( www.sse.com.cn )刊發了以下公告。茲載列如下，僅供參閱。 承董事會命 江蘇恒瑞醫藥股份有限公司 董事長 孫飄揚先生 证券代码：600276 证券简称：恒瑞医药 公告编号：临 2025-183 江苏恒瑞医药股份有限公司 关于获得药物临床试验批准通知书的公告 本公司董事会及全体董事保证本公告内容不存在任何虚假记载、误导性陈述 或者重大遗漏，并对其内容的真实性、准确性和完整性承担法律责任。 近日，江苏恒瑞医药股份有限公司（以下简称"公司"）及子 ...

Core Viewpoint - The company has received approval from the National Medical Products Administration for clinical trials of SHR-1139 injection, a self-developed biopharmaceutical with no similar drugs approved in the market [1] Group 1: Company Developments - The company’s subsidiary, Guangdong Hengrui Medicine Co., Ltd., has been authorized to conduct clinical trials for SHR-1139 injection [1] - The total research and development investment for the SHR-1139 injection project has reached approximately 100.13 million yuan [1] Group 2: Market Context - Currently, there are no similar drugs approved for market use domestically or internationally, indicating a potential unique market position for SHR-1139 injection [1]

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所產生或因依賴 該等內容而引致的任何損失承擔任何責任。 （股份代號：1276） 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條刊發。 根據中華人民共和國的有關法例規定，江蘇恒瑞醫藥股份有限公司（「本公司」）在 上海證券交易所網站( www.sse.com.cn )刊發了以下公告。茲載列如下，僅供參閱。 Jiangsu Hengrui Pharmaceuticals Co., Ltd. 江蘇恒瑞醫藥股份有限公司 （於中華人民共和國註冊成立的股份有限公司） 承董事會命 江蘇恒瑞醫藥股份有限公司 董事長 孫飄揚先生 中國上海 2025年11月21日 於本公告日期，董事會成員包括(i)執行董事孫飄揚先生、戴洪斌先生、馮佶女 士、張連山先生、江寧軍先生及孫杰平先生；(ii)非執行董事郭叢照女士；及(iii) 獨立非執行董事董家鴻先生、曾慶生先生、孫金雲先生及周紀恩先生。 证券代码：600276 证券简称：恒瑞医药 公告编号：临 2025-1 ...

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所產生或因依賴 該等內容而引致的任何損失承擔任何責任。 Jiangsu Hengrui Pharmaceuticals Co., Ltd. 江蘇恒瑞醫藥股份有限公司 （於中華人民共和國註冊成立的股份有限公司） （股份代號：1276） 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條刊發。 根據中華人民共和國的有關法例規定，江蘇恒瑞醫藥股份有限公司（「本公司」）在 上海證券交易所網站( www.sse.com.cn )刊發了以下公告。茲載列如下，僅供參閱。 承董事會命 江蘇恒瑞醫藥股份有限公司 董事長 孫飄揚先生 中國上海 2025年11月21日 於本公告日期，董事會成員包括(i)執行董事孫飄揚先生、戴洪斌先生、馮佶女 士、張連山先生、江寧軍先生及孫杰平先生；(ii)非執行董事郭叢照女士；及(iii) 獨立非執行董事董家鴻先生、曾慶生先生、孫金雲先生及周紀恩先生。 本公司董事会及全体董事保证本公告内容不存在任何虚假记载、误导性陈述 或 ...