Junshi Biosciences(688180)

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君实生物(688180) - 君实生物关于持股5%以上股东减持股份计划的公告

2025-08-14 12:18
上海君实生物医药科技股份有限公司 关于持股 5%以上股东减持股份计划的公告 本公司董事会、全体董事及相关股东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、准确性和完整性依法承担法律 责任。 重要内容提示: 大股东持股的基本情况 截至本公告披露日,上海檀英投资合伙企业(有限合伙)(以下简称"上海 檀英")持有上海君实生物医药科技股份有限公司(以下简称"公司"或"君实 生物")股份 71,459,326 股,股份性质为 A 股,占公司总股本的 6.9602%。上述 股份为公司首次公开发行股票并在上海证券交易所科创板上市(以下简称"IPO") 前取得的股份,且已于 2021 年 7 月 15 日起解除限售并上市流通。 减持计划的主要内容 上海檀英长期看好公司的发展,因基金期限与流动性资金安排原因,计划通 过大宗交易的方式减持其持有的公司股份数量不超过 20,533,797 股,减持比例不 超过公司总股本的 2%。上海檀英为在中国证券投资基金业协会备案的私募基金, 已成功申请适用《上市公司创业投资基金股东减持股份的特别规定》和《上海证 券交易所上市公司创业投资基金股东减持股份实施细则 ...
君实生物(688180.SH):上海檀英拟大宗交易减持不超过2%股份
Ge Long Hui A P P· 2025-08-14 11:35
格隆汇8月14日丨君实生物(688180.SH)公布,上海檀英长期看好公司的发展,因基金期限与流动性资金 安排原因,计划通过大宗交易的方式减持其持有的公司股份数量不超过2053.38万股,减持比例不超过 公司总股本的2%。拟通过大宗交易方式减持的,在任意连续60日内减持股份的总数不超过公司总股本 的2%,自本公告披露之日起15个交易日后的三个月内进行。上述股份的减持价格按市场价格确定。 ...
君实生物(688180) - 君实生物H股公告

2025-08-14 09:30
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,概不對因本公告全部或任何部分內容而產生或因倚 賴該等內容而引致的任何損失承擔任何責任。 上海君實生物醫藥科技股份有限公司(「本公司」及其附屬公司「本集團」)董事會 (「董事會」)茲通告謹定於2025年8月26日(星期二)舉行董事會會議,以考慮及通 過本集團截至2025年6月30日止六個月的中期業績,以及處理其他事項。 承董事會命 上海君實生物醫藥科技股份有限公司 熊俊先生 主席 中國,上海,2025年8月14日 於本公告日期,本公司董事會包括執行董事熊俊先生、李寧博士、鄒建軍博士、 李聰先生、張卓兵先生、姚盛博士、王剛博士及李鑫博士;非執行董事湯毅先 生;以及獨立非執行董事張淳先生、馮曉源博士、楊悅博士、酈仲賢先生及魯琨 女士。 * 僅供識別之用 SHANGHAI JUNSHI BIOSCIENCES CO., LTD.* 上海君實生物醫藥科技股份有限公司 (於中華人民共和國註冊成立的股份有限公司) (股份代號:1877) 董事會召開日期 ...
君实生物(01877) - 董事会召开日期

2025-08-14 08:30
上海君實生物醫藥科技股份有限公司(「本公司」及其附屬公司「本集團」)董事會 (「董事會」)茲通告謹定於2025年8月26日(星期二)舉行董事會會議,以考慮及通 過本集團截至2025年6月30日止六個月的中期業績,以及處理其他事項。 SHANGHAI JUNSHI BIOSCIENCES CO., LTD.* 上海君實生物醫藥科技股份有限公司 (於中華人民共和國註冊成立的股份有限公司) (股份代號:1877) 董事會召開日期 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,概不對因本公告全部或任何部分內容而產生或因倚 賴該等內容而引致的任何損失承擔任何責任。 承董事會命 上海君實生物醫藥科技股份有限公司 熊俊先生 主席 中國,上海,2025年8月14日 於本公告日期,本公司董事會包括執行董事熊俊先生、李寧博士、鄒建軍博士、 李聰先生、張卓兵先生、姚盛博士、王剛博士及李鑫博士;非執行董事湯毅先 生;以及獨立非執行董事張淳先生、馮曉源博士、楊悅博士、酈仲賢先生及魯琨 女士。 * 僅供識別之用 ...
君实生物涨5.03%,成交额10.25亿元,近5日主力净流入1473.18万
Xin Lang Cai Jing· 2025-08-13 08:13
来源:新浪证券-红岸工作室 8月13日,君实生物涨5.03%,成交额10.25亿元,换手率3.12%,总市值446.20亿元。 异动分析 创新药+生物疫苗+猴痘概念 1、2024年年报,公司具备完整的从创新药物的发现和开发、 在全球范围内的临床研究、 大规模生产到 商业化的全产业链能力, 旨在成为立足中国、 布局全球的创新医药公司。 公司坚持质量为本、 求真务 实、 诚信合规、 追求卓越的企业价值观, 致力于通过源头创新以及合作开发等形式来研发 first-in-class (同类首创)或 best-in-class(同类最优) 的药物。 通过卓越的创新药物发现能力、 强大的生物技术研 发能力和大规模生产能力, 公司已成功开发出极具市场潜力的药品组合, 多项产品具有里程碑意义: 核心产品之一特瑞普利单抗是国内首个获得 NMPA 批准上市的国产抗 PD-1 单克隆抗体, 截至本报告 披露日已在中国内地获批 11 项适应症, 另有一项 sNDA 已受理, 其中多项为公司独家或领先适应 症, 特瑞普利单抗还是 FDA 批准上市的首个中国自主研发和生产的创新生物药, 截至本报告披露日, 特瑞普利单抗已在中国内地、 中 ...
君实生物涨2.01%,成交额2.57亿元,主力资金净流入827.18万元
Xin Lang Cai Jing· 2025-08-13 02:48
来源:新浪证券-红岸工作室 资料显示,上海君实生物医药科技股份有限公司位于上海市浦东新区平家桥路100弄6号7幢16层,香港铜 锣湾希慎道33号利园1期19楼1918室,成立日期2012年12月27日,上市日期2020年7月15日,公司主营业 务涉及单克隆抗体药物和其他治疗型蛋白药物的研发与产业化,单克隆抗体药物研发的技术服务与技术 转让等。主营业务收入构成为:药品销售84.18%,技术许可及特许权使用收入12.08%,其他(补 充)3.73%。 君实生物所属申万行业为:医药生物-生物制品-其他生物制品。所属概念板块包括:猴痘概念、中盘、 融资融券、增持回购、生物医药等。 截至3月31日,君实生物股东户数2.94万,较上期增加0.24%;人均流通股25987股,较上期减少0.23%。 2025年1月-3月,君实生物实现营业收入5.01亿元,同比增长31.46%;归母净利润-2.35亿元,同比增长 17.01%。 机构持仓方面,截止2025年3月31日,君实生物十大流通股东中,华夏上证科创板50成份ETF (588000)位居第六大流通股东,持股3025.34万股,相比上期减少505.06万股。易方达上证科创板 ...
君实生物-U股价上涨2.48% 特瑞普利单抗第13项适应症申请获受理
Jin Rong Jie· 2025-08-11 10:49
截至2025年8月11日15时,君实生物-U最新股价为42.54元,较前一交易日上涨1.03元,涨幅2.48%。当 日开盘价为41.60元,最高触及43.50元,最低下探40.81元,成交量为23.09万手,成交金额达9.67亿元。 风险提示:医药研发存在不确定性,市场竞争加剧可能导致产品销售不及预期。 本文源自:金融界 作者:A股君 公司近期公告显示,特瑞普利单抗联合维迪西妥单抗用于HER2表达的局部晚期或转移性尿路上皮癌患 者的新适应症上市申请已获国家药监局受理。这是特瑞普利单抗在国内申报的第13项适应症。 2025年8月11日,君实生物-U主力资金净流出1562.72万元,占流通市值的0.05%。近五个交易日累计主 力资金净流出4099.42万元,占流通市值的0.13%。 君实生物-U属于生物医药行业,专注于创新药物的研发、生产和商业化。公司主要产品包括特瑞普利 单抗等生物药,覆盖肿瘤免疫治疗、代谢疾病、自身免疫性疾病等领域。 ...
启迪药业控制权将变更;硕世生物上半年净利润同比降逾八成丨医药早参
Mei Ri Jing Ji Xin Wen· 2025-08-10 23:21
Group 1 - Tsinghua Unigroup's control will change as Hunan Sailuxian will acquire approximately 58.61 million shares from its controlling shareholder, Tsinghua Technology Service Co., Ltd, leading to a shift in control of Tsinghua Unigroup [1] - The new controlling shareholder will need to stabilize the company's operations amidst industry consolidation, and investors should pay attention to future asset integration and the new shareholder's resource injection capabilities, with potential short-term stock price volatility [1] Group 2 - Shuoshi Bio reported a revenue of 176 million yuan, a year-on-year decrease of 1.05%, and a net profit attributable to shareholders of 3.99 million yuan, down 86.35% year-on-year, primarily due to the deepening of centralized procurement in the in vitro diagnostic industry and an increase in the VAT rate to 13% [2] - The decline in net profit is attributed to pressure on product prices from industry procurement, a significant drop in gross margin, and a 13.11% reduction in R&D investment, which may weaken long-term competitiveness [2] Group 3 - Fosun Pharma's subsidiary, Shanghai Fuhong Hanlin Biotech, received FDA approval to conduct Phase I clinical trials for HLX43, a targeted PD-L1 antibody-drug conjugate for thymic cancer, marking a significant step in the internationalization of innovative drugs [3] - The drug's dual advantages of immune modulation and precise targeting position it competitively in the global market, with the potential to fill a treatment gap for thymic cancer if subsequent data is positive [3] Group 4 - Junshi Biosciences announced that the National Medical Products Administration has accepted the application for the 13th indication of its PD-1 monoclonal antibody, Toripalimab, for use in combination with HER2 ADC for patients with locally advanced or metastatic urothelial carcinoma expressing HER2 [4] - This combination is expected to further strengthen Junshi's differentiated positioning in the PD-1 market and enhance collaboration with Rongchang Bio on ADC development [4]
新药周观点:创新药6月进院数据更新,多个新纳入医保创新药快速进院-20250810
Guotou Securities· 2025-08-10 11:03
Investment Rating - The report maintains an investment rating of "Outperform" with a target price set for leading stocks [3][4]. Core Insights - The innovative drug sector is experiencing fluctuations, but several catalysts are anticipated, including academic conferences, business development achievements, and negotiations for medical insurance [2]. - The National Medical Insurance Administration has updated the data on innovative drugs included in the medical insurance directory, showing rapid hospital admissions for several newly included domestic innovative drugs [2][22]. Summary by Sections Weekly New Drug Market Review - From August 4 to August 10, 2025, the top five companies in the new drug sector by stock price increase were: Beihai Kangcheng (+73.1%), Jiahe Biotech (+39.0%), Gilead Sciences (+30.3%), Heyu Biotech (+21.1%), and Hengrui Medicine (+15.3%). The top five companies with the largest declines were: Hutchison China MediTech (-13.8%), Frontier Biotech (-13.4%), Yifang Biotech (-11.7%), Haichuang Pharma (-9.9%), and Maiwei Biotech (-9.2%) [1][16]. Recommended Stocks to Watch - The report suggests focusing on potential overseas licensing opportunities for significant products, including differentiated GLP-1 assets from companies like Zhongsheng Pharma, Kangyuan Pharma, and Gilead Sciences. Additionally, upgraded PD-1 products from Kangfang Biotech and others are highlighted [2][22]. Key Analysis of the New Drug Industry - The report notes that several innovative drugs newly included in the medical insurance directory are rapidly entering hospitals, with notable growth in hospital admissions for drugs such as Zaiqiang Pharma's recombinant thrombin and Hengrui Medicine's Tazemetostat [2][22][23]. New Drug Approval and Acceptance Status - This week, three new drug applications were approved, including Adalimumab injection from Wuhan Biological Products Research Institute, Dulaglutide injection from Shandong Boan Biotech, and Evinacumab injection from Xi'an Janssen [28][29]. Additionally, four new drug applications were accepted, including Trastuzumab injection from Amgen and others [28][30]. Clinical Application Approval and Acceptance Status - A total of 55 new drug clinical applications were approved this week, while 31 new drug clinical applications were accepted [10][31].
君实生物(1877.HK):创新突围 再启新程
Ge Long Hui· 2025-08-10 03:00
Core Viewpoint - Junshi Biosciences, a leading domestic BioPharma company, is experiencing accelerated sales growth in its existing business and is on the verge of significant advancements in its innovative drug pipeline [1][3] Group 1: Sales Performance - Junshi Biosciences' core product, Toripalimab, is projected to achieve sales of 1.501 billion yuan in 2024, representing a 66% year-on-year growth, indicating a return to sales momentum [1] - The subcutaneous formulation of Toripalimab is currently in Phase III clinical trials, which, upon approval, is expected to further solidify the product's market position [1] Group 2: Innovative Drug Pipeline - Multiple innovative assets are approaching critical stages, with several candidates expected to enter Phase III clinical trials soon, including JS203 (CD20/CD3), JS107 (CLDN18.2 ADC), JS207 (PD-1/VEGF), JT002 (siRNA), and JS015 (DKK1) [2] - The JS107 asset is leading in the domestic development of CLDN18.2 ADC, showing excellent efficacy and safety, and may become one of the first approved treatments for first-line gastric cancer [2] - JS207, a PD-1/VEGF dual antibody, is positioned competitively in the market and has initiated multiple Phase II clinical studies in combination therapies, potentially allowing it to outperform competitors [2] - JS015, a globally leading DKK1 monoclonal antibody, has demonstrated impressive data in early trials, achieving a 100% overall response rate (ORR) in evaluable patients for first-line colorectal cancer treatment [2] Group 3: Early Pipeline and Technology Platforms - The company has a rich early-stage pipeline and a comprehensive technology platform, including dual antibodies, dual antibody-drug conjugates (ADCs), and small nucleic acids [2] - The company is also developing a PD-1/IL-2 dual antibody (JS213) with promising early data in Australian solid tumors, which could become a significant product in the next generation of immuno-oncology [2] - JT002, a licensed nasal spray immunomodulatory small nucleic acid drug targeting seasonal allergic rhinitis, has completed patient enrollment in Phase II clinical trials [2] - JS212 (EGFR/HER3 dual antibody ADC) has received clinical approval, further enhancing the company's asset portfolio [2] Group 4: Financial Projections - Revenue projections for Junshi Biosciences are estimated at 2.681 billion yuan, 3.673 billion yuan, and 5.479 billion yuan for the years 2025 to 2027, respectively [3] - The company is expected to report net losses of 940 million yuan, 350 million yuan, and a profit of 420 million yuan for the same period, with corresponding earnings per share (EPS) of -0.92 yuan, -0.34 yuan, and 0.41 yuan [3] - The company is rated as a "buy" based on its growth potential and upcoming product launches [3]