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恒瑞医药(01276.HK):注射用SHR-A2102、阿得贝利单抗注射液获批开展临床试验
Ge Long Hui· 2025-08-13 09:18
注射用 SHR-A2102 为公司自主研发且具有知识产权的靶向 Nectin-4 的抗体药物偶联物(ADC),其有效 载荷是拓扑异构酶Ⅰ抑制剂(TOP1i)。多种研究表明 Nectin-4 在肿瘤中的高表达与肿瘤的发展和不良预 后密切相关。目前全球共有 1 款同类产品获批上市,为 Enfortumab vedotin(商品名:Padcev),经查询 EvaluatePharma 数据库,2024 年该产品全球销售额约为 19.49 亿美元。截至目前,注射用 SHR-A2102 相关项目累计研发投入约 20,547 万元。 阿得贝利单抗注射液是公司自主研发的人源化抗 PD-L1 单克隆抗体,能通过特异性结合 PD-L1 分子从 而阻断导致肿瘤免疫耐受的 PD-1/PD-L1 通路,重新激活免疫系统的抗肿瘤活性,从而达到治疗肿瘤的 目的。公司阿得贝利单抗注射液(商品名:艾瑞利)已于 2023 年 3 月获批上市,获批的适应症为与卡铂 和依托泊苷联合用于广泛期小细胞肺癌患者的一线治疗。国外有同类产品Atezolizumab ( 商 品 名 : Tecentriq ) 、 Avelumab( 商 品 名 : Bave ...
恒瑞医药两款药品纳入拟突破性治疗品种公示名单
Zheng Quan Shi Bao Wang· 2025-08-11 10:59
Core Viewpoint - Heng Rui Medicine's subsidiary has two products, SHR-A1811 and Abedilizumab, included in the list of proposed breakthrough therapies by the National Medical Products Administration, marking the ninth inclusion for SHR-A1811 [1] Group 1: Market Context - Breast cancer is the second most common malignant tumor globally, with approximately 2.297 million new cases reported in 2022 [1] - In China, breast cancer accounts for 15.6% of all malignant tumors, with around 357,000 new cases and 75,000 deaths in 2022 [2] - Triple-negative breast cancer (TNBC) represents 10%-15% of all breast cancer cases, predominantly affecting younger women and exhibiting high invasiveness and poor prognosis [2] Group 2: Product Information - SHR-A1811 is an injectable drug that targets HER2-positive tumors, approved for use in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who have received prior systemic therapy [3] - The global sales of similar products, Kadcyla and Enhertu, are projected to reach approximately $6.557 billion in 2024 [3] - The total R&D investment for SHR-A1811 has reached approximately 1.259 billion yuan [3] Group 3: Competitive Landscape - Abedilizumab is a humanized anti-PD-L1 monoclonal antibody, approved for first-line treatment of extensive-stage small cell lung cancer [4] - Similar products like Atezolizumab, Avelumab, and Durvalumab are projected to have a combined global sales of approximately $9.648 billion in 2024 [4] - The total R&D investment for Abedilizumab has reached approximately 901 million yuan [4]
恒瑞医药4款药物临床获批 累计研发超20亿元
Zheng Quan Shi Bao Wang· 2025-07-17 10:15
Core Viewpoint - Heng Rui Medicine has received approval from the National Medical Products Administration for clinical trials of four drugs, indicating a significant advancement in its oncology pipeline [1][2][3][4] Group 1: Drug Approvals and Clinical Trials - The company and its subsidiaries have been granted clinical trial approval for SHR-8068 injection, Adebali monoclonal antibody injection, Bevacizumab injection, and Apatinib mesylate tablets [1][2][3][4] - SHR-8068 is a fully human anti-CTLA-4 monoclonal antibody aimed at enhancing anti-tumor immune effects, with a cumulative R&D investment of approximately 214 million yuan [1] - Adebali monoclonal antibody injection, a humanized anti-PD-L1 monoclonal antibody, was approved in March 2023 for first-line treatment of extensive-stage small cell lung cancer, with a cumulative R&D investment of about 887 million yuan [2] - Bevacizumab injection, a humanized anti-VEGF monoclonal antibody, was approved in June 2021, with a cumulative R&D investment of around 345 million yuan [3] - Apatinib mesylate tablets have been approved for three indications, with a cumulative R&D investment of approximately 587 million yuan [4] Group 2: Market Potential and Competitors - The global sales of similar products for SHR-8068, including Ipilimumab and Tremelimumab, are projected to be approximately 3.271 billion USD in 2024 [1] - The combined global sales for Adebali's competitors, Atezolizumab, Avelumab, and Durvalumab, are estimated to be around 9.648 billion USD in 2024 [2] - Bevacizumab's global sales are projected to be about 5.655 billion USD in 2024 [3] - The global sales for Apatinib's competitors, including Sorafenib, Sunitinib, and Pazopanib, are expected to total approximately 543 million USD in 2024 [4]
恒瑞医药(600276) - 恒瑞医药关于获得药物临床试验批准通知书的公告
2025-02-27 08:15
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 阿得贝利单抗注射液是公司自主研发的人源化抗 PD-L1 单克隆抗体,能通过 特异性结合 PD-L1 分子从而阻断导致肿瘤免疫耐受的 PD-1/PD-L1 通路,重新激 活免疫系统的抗肿瘤活性,从而达到治疗肿瘤的目的。国外有同类产品 Atezolizumab ( 商 品 名 : Tecentriq ) 、 Avelumab( 商品名: Bavencio) 和 Durvalumab(商品名:Imfinzi)于美国获批上市销售,其中 Atezolizumab 和 Durvalumab 已在中国获批上市。国内有康宁杰瑞/思路迪药业的恩沃利单抗、基 石药业的舒格利单抗和正大天晴药业的贝莫苏拜单抗等同类产品获批上市。公司 阿得贝利单抗注射液(商品名:艾瑞利)已于 2023 年 3 月获批上市,获批的适 应症为与卡铂和依托泊苷联合用于广泛期小细胞肺癌患者的一线治疗。经查询, 2023 年 Atezolizumab、Avelumab 和 Durvalumab 全球销售额合计约为 89.85 亿 美元。截至目前,阿得贝利单抗注射液相关项目累计研发投入约 78,47 ...