Core Viewpoint - Heng Rui Medicine has achieved record high operating performance driven by its innovative drugs, with significant revenue and profit growth in the first half of 2025 [1][4]. Financial Performance - In the first half of 2025, Heng Rui Medicine reported revenue of 15.761 billion yuan, a year-on-year increase of 15.88%, and a net profit attributable to shareholders of 4.450 billion yuan, up 29.67% [1][4]. - The company has maintained a three-year trend of increasing both revenue and net profit since the mid-2023 [2]. - The revenue from innovative drug sales and licensing reached 9.561 billion yuan, accounting for 60.66% of total revenue [2][7]. - Quarterly performance showed revenue of 7.206 billion yuan and 8.556 billion yuan for Q1 and Q2 respectively, with year-on-year growth of 20.14% and 12.53% [5][6]. Innovation and R&D - Heng Rui Medicine has significantly increased its R&D investment, totaling 3.871 billion yuan in the first half of 2025, which is 24.56% of its revenue [2][10]. - The company ranks second globally in the number of self-developed drug pipelines [3][12]. - Heng Rui has submitted five new drug applications in the first half of 2025 and has over 100 self-innovated products in clinical development [10]. Licensing and International Expansion - The company has achieved notable success in international markets, receiving upfront payments of 200 million USD from Merck Sharp & Dohme and 75 million USD from IDEAYA, contributing to revenue growth [2][7]. - Innovative drug licensing has become a regular business for Heng Rui, significantly impacting its revenue structure [7]. Market Position and Future Outlook - Heng Rui Medicine aims to establish itself as a leading innovative pharmaceutical company rooted in China with a highly differentiated product matrix [10]. - The company is focused on addressing unmet medical needs across various therapeutic areas, including oncology, metabolic diseases, and immunology [12].

Core Insights - The company reported a revenue of approximately RMB 15.761 billion for the first half of 2025, representing a year-on-year growth of 15.9% [1] - Net profit attributable to shareholders was RMB 4.45 billion, reflecting a year-on-year increase of 29.7% [1] - Basic earnings per share were RMB 0.70 [1] Revenue Breakdown - The growth in revenue and profit was primarily driven by increased sales and licensing income from innovative drugs, which amounted to RMB 9.561 billion, a year-on-year increase of 26.8%, accounting for 60.7% of total revenue [1] - Sales revenue from innovative drugs reached RMB 7.57 billion [1] Innovative Drug Performance - Key innovative drugs such as Rivoceranib, Darsylin, and Henggrelizumab have effectively addressed unmet clinical needs, with strong clinical data gaining recognition from doctors and patients, leading to continued rapid revenue growth [1] - Earlier launched innovative drugs like Arixtra, Remimazolam, Pyrotinib, and Fluorouracil have expanded their application scope due to accumulating post-market research evidence and new indications, contributing to sales revenue [1] - Other innovative products like Apatinib, Sulfapyridine, and Hecuqipob have also seen growth during the reporting period [1] Licensing Income - The company recognized licensing income as a regular business activity, with significant payments received from Merck Sharp & Dohme (USD 200 million) and IDEAYA Biosciences (USD 75 million), further boosting operational performance [2] Generic Drug Performance - Although sales revenue from generic drugs included in centralized procurement experienced a slight decline, high-quality generic products such as Liposomal Bupivacaine and the first approved generic product of Albumin-bound Paclitaxel in the U.S. saw rapid revenue growth, leading to a slight overall increase in generic drug business revenue [2]

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8月20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。 江苏恒瑞医药股份有限公司 2025 年半年度报告 公司代码：600276 ...

Core Viewpoint - The report by MoSheng Consulting focuses on colony-stimulating factor (CSF) drugs, analyzing their classification, market landscape, clinical applications, and market trends for 2024. Group 1: Overview of Bone Marrow Suppression and Colony-Stimulating Factors - Chemotherapy is a cornerstone treatment for tumors, but bone marrow suppression is a major adverse effect, leading to neutropenia, thrombocytopenia, and tumor-related anemia [1][9] - Neutropenia, occurring at a high incidence, can affect chemotherapy efficacy and increase the risk of infection and mortality. Recombinant human granulocyte colony-stimulating factor (rhG-CSF) and pegylated rhG-CSF (PEG-rhG-CSF) are effective drugs for preventing and treating neutropenia [1][15] Group 2: Classification and Mechanism of Action of Colony-Stimulating Factors - Colony-stimulating factors mainly include granulocyte colony-stimulating factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF). G-CSF promotes hematopoietic stem cell proliferation and regulates neutrophil production [1][12] - G-CSF is further divided into rhG-CSF, PEG-rhG-CSF, and rhGM-CSF, each with different indications, mechanisms of action, and pharmacokinetic characteristics [1][21] Group 3: Market Competition Landscape - The G-CSF market has grown nearly 3.5 times from 2015 to 2023, peaking at 10.31 billion in 2022. PEG-rhG-CSF has a market share of 69.65%, becoming the mainstream product, while rhG-CSF maintains stable sales around 3 billion [2][28] - The domestic rhG-CSF market is competitive, with Qilu Pharmaceutical as the leading company. Currently, seven PEG-rhG-CSF products have been approved for market, and the first-generation products have largely released their volume benefits, with some price declines expected for a second wave of growth [2][26] Group 4: Market Trend Analysis - The PEG-rhG-CSF market is expected to remain relatively stable in the coming years, with only a few products in the pipeline. The development of rhG-CSF in reproductive fields is a future direction, although further research is needed [2][28] - Trastuzumab, as a cyclin-dependent kinase 4/6 inhibitor, can reduce hematological toxicity and the usage rate of G-CSF [2][28]

Investment Rating - The report maintains an investment rating of "Outperform the Market - A" for the biopharmaceutical sector [4]. Core Insights - The report highlights that Heng Rui Medicine has updated its innovative drug pipeline, entering a harvest period with 19 Class 1 innovative drugs approved for market, 11 in NDA stage, and 16 in Phase 3 clinical trials [2][18]. Summary by Sections Weekly New Drug Market Review - From March 31 to April 4, 2025, the top five companies in the new drug sector by stock price increase were: Hai Chuang Pharmaceutical (20.74%), Yi Ming An Ke (17.89%), Jia He Bio (15.20%), Kang Fang Bio (15.15%), and Mai Wei Bio (12.25%). The top five companies with the largest declines were: Chuang Sheng Group (-24.18%), Teng Sheng Bo Yao (-19.92%), He Bo Pharmaceutical (-17.76%), Mai Bo Pharmaceutical (-17.19%), and Ge Li Pharmaceutical (-12.75%) [1][14]. Key Analysis of the New Drug Industry - Heng Rui Medicine's 2024 annual report reveals its latest research pipeline as of March 2025, with 19 Class 1 innovative drugs approved, 11 in NDA stage, and 16 in Phase 3 clinical trials. The approved drugs include various treatments across oncology, metabolism, immunology, and cardiovascular fields [2][18][20]. New Drug Approvals and Acceptance - In the week, 10 new drugs or new indications were approved for market, 37 new drugs received IND approval, 19 new drugs had IND applications accepted, and 5 new drugs had NDA applications accepted [9][22]. Domestic New Drug Industry Focus - Key highlights include Heng Rui Medicine's JAK1 inhibitor, Aima Xitini (SHR0302), receiving approval for a new indication for adult patients with moderate to severe active rheumatoid arthritis. Additionally, the company has initiated Phase 3 clinical trials for its GLP-1 receptor agonist, HRS-7535, aimed at weight loss [10][30].