Junshi Biosciences(688180)
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君实生物(01877)获董事长熊俊累计增持10万股

智通财经网· 2026-02-10 11:27
智通财经APP讯,君实生物(01877)公布控股股东、实际控制人之一兼董事长增持股份进展,截至本公告 披露日,熊俊先生通过上海证券交易所系统以集中竞价方式累计增持公司 A 股股份10万股,约占公司 总股本的 0.01%,累计成交总额为人民币 383.84 万元。本次增持计划尚未实施完毕,熊俊先生将继续 按照相关增持计划,在增持计划实施期间内择机增持公司股份。 ...
君实生物(01877.HK)获控股股东兼董事长熊俊累计增持10万股公司A股

Ge Long Hui A P P· 2026-02-10 11:25
格隆汇2月10日丨君实生物(01877.HK)公告,上海君实生物医药科技股份有限公司控股股东、实际控制 人之一兼董事长熊俊拟自2025年4月12日起12个月内,通过上海证券交易所交易系统与香港联合交易所 有限公司允许的方式(包括但不限于集中竞价和大宗交易等方式)增持公司A股股份及H股股份,合计增 持金额不低于人民币1亿元,其中A股增持金额不低于人民币5,000万元。 截至本公告披露日,熊俊通过上海证券交易所系统以集中竞价方式累计增持公司A股股份10万股,约占 公司总股本的0.01%,累计成交总额为人民币383.84万元。本次增持计划尚未实施完毕,熊俊将继续按 照相关增持计划,在增持计划实施期间内择机增持公司股份。 ...
君实生物(01877) - 海外监管公告 - 上海君实生物医药科技股份有限公司关於控股股东、实际控制...

2026-02-10 11:16
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之內容概不負責,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。 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) 茲載列上海君實生物醫藥科技股份有限公司在上海證券交易所網站刊發之《上海 君實生物醫藥科技股份有限公司關於控股股東、實際控制人之一兼董事長增持股 份進展公告》,僅供參閱。 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,2026年2月10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、酈仲賢先生、魯琨女士及楊勁 博士。 * 僅供識別之用 (股份代號:1877) 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條規則作出。 证券代码:688180 证券简称:君实生 ...
君实生物(688180) - 君实生物关于控股股东、实际控制人之一兼董事长增持股份进展公告

2026-02-10 09:32
上海君实生物医药科技股份有限公司 关于控股股东、实际控制人之一兼董事长 增持股份进展公告 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。 证券代码:688180 证券简称:君实生物 公告编号:临 2026-004 重要内容提示: 上海君实生物医药科技股份有限公司(以下简称"公司")控股股东、 实际控制人之一兼董事长熊俊先生拟自 2025 年 4 月 12 日起 12 个月内,通过上 海证券交易所交易系统与香港联合交易所有限公司允许的方式(包括但不限于集 中竞价和大宗交易等方式)增持公司 A 股股份及 H 股股份,合计增持金额不低 于人民币 1 亿元,其中 A 股增持金额不低于人民币 5,000 万元。 截至本公告披露日,熊俊先生通过上海证券交易所系统以集中竞价方式 累计增持公司 A 股股份 100,000 股,约占公司总股本的 0.01%,累计成交总额为 人民币 383.84 万元。本次增持计划尚未实施完毕,熊俊先生将继续按照相关增 持计划,在增持计划实施期间内择机增持公司股份。 本次增持计划可能存在因资本市场 ...
君实生物:实际控制人之一兼董事长熊俊累计增持10万股公司A股股份

Ge Long Hui· 2026-02-10 09:20
格隆汇2月10日丨君实生物(688180.SH)公布,截至本公告披露日,控股股东、实际控制人之一兼董事长 熊俊先生通过上海证券交易所系统以集中竞价方式累计增持公司A股股份10万股,约占公司总股本的 0.01%,累计成交总额为人民币383.84万元。本次增持计划尚未实施完毕,熊俊先生将继续按照相关增 持计划,在增持计划实施期间内择机增持公司股份。 ...
君实生物邹建军:双轨并行守初心 破局生长赴新程|生物医药大健康2026思享汇
Jin Rong Jie· 2026-02-10 09:04
Core Insights - The Chinese biopharmaceutical industry is at a pivotal moment as it transitions from "scale and speed" to "quality and value" during the end of the 14th Five-Year Plan and the beginning of the 15th Five-Year Plan [1][3] - The company emphasizes the importance of innovation, dual-track development, and value orientation to navigate the challenges and opportunities in 2026 [1][4] Group 1: Industry Transition - The industry is experiencing a transformation focused on quality and value, moving away from previous growth models based on scale and speed [1][3] - The company aims to address the challenges of homogenization and competition by focusing on original innovation and differentiated strategies [3][4] Group 2: Globalization and Market Expansion - The company has established a global commercialization network covering over 80 countries and regions, with products launched in 40 international markets [2] - The strategy includes enhancing local patient access while expanding global partnerships to overcome international market entry barriers [4] Group 3: Innovation and Technology - The company is committed to deepening its innovation in the field of tumor immunotherapy, particularly in addressing PD-(L)1 inhibitor resistance [3] - AI technology is being leveraged to optimize operational efficiency and enhance quality, aligning with the industry's focus on sustainable development [4]
君实生物涨0.90%,成交额3.32亿元,后市是否有机会?
Xin Lang Cai Jing· 2026-02-10 07:53
Core Viewpoint - Junshi Biosciences is actively developing a monkeypox recombinant protein vaccine in collaboration with several prestigious institutions, indicating a strong focus on innovative vaccine development and a commitment to expanding its product pipeline in the biopharmaceutical sector [2][3]. Company Developments - On October 27, 2023, Junshi Biosciences announced a partnership with Peking University, the Institute of Microbiology of the Chinese Academy of Sciences, Shanxi Higher Innovation Research Institute, and Beihang University to jointly develop a monkeypox recombinant protein vaccine [2]. - The company’s subsidiary, Junshi Biotech, is involved in the development of various vaccine-related products, including monkeypox and Zika vaccines, which are currently in the preclinical development stage [2]. Product Pipeline and Achievements - Junshi Biosciences has a comprehensive capability in the entire industry chain from drug discovery and development to large-scale production and commercialization, aiming to become a global innovative pharmaceutical company based in China [3]. - The company’s core product, Toripalimab, is the first domestically approved PD-1 monoclonal antibody in China, with 11 approved indications and one supplemental NDA under review. It has also received approvals in multiple countries including the U.S., EU, and Australia [3]. - The company is advancing its proprietary drug tifcemalimab, which is the first anti-BTLA monoclonal antibody to enter clinical development, with ongoing Phase III clinical trials and several Phase Ib/II studies in various tumor types [3]. Financial Performance - For the period from January to September 2025, Junshi Biosciences reported revenue of 1.806 billion yuan, representing a year-on-year growth of 42.06%. However, the net profit attributable to shareholders was a loss of 596 million yuan, although this reflects a 35.72% improvement compared to the previous year [9]. Technological Advancements - The company has deployed an AI translation platform that has replaced over 80% of external translation services for scientific literature, clinical trials, and quality management, enhancing operational efficiency [4]. Market Position - As of February 10, 2023, Junshi Biosciences had a market capitalization of 36.673 billion yuan, with a trading volume of 3.32 billion yuan and a turnover rate of 1.21% [1].
驱动基因阴性NSCLC专题:下一代治疗范式:双抗、IO+ADC
Southwest Securities· 2026-02-10 03:06
Investment Rating - The report does not explicitly state an investment rating for the industry Core Insights - The proportion of driver gene-negative non-small cell lung cancer (NSCLC) patients is approximately 31% in both China and the United States, indicating a significant market opportunity for treatments targeting this demographic [2][15] - The estimated market size for immune drugs used in first-line treatment of driver gene-negative NSCLC is projected to be around 7.5 billion CNY (approximately 1.1 billion USD) in China and 18 billion CNY (approximately 2.7 billion USD) in the United States by 2030 [2] - The current first-line treatment for advanced driver gene-negative NSCLC primarily relies on PD(L)-1 inhibitors combined with chemotherapy, but there are limitations in long-term efficacy and options for patients intolerant to chemotherapy [3] Summary by Sections Section 1: NSCLC Global Overview - Lung cancer is the leading cancer type globally, with new cases accounting for approximately 12% of all cancer cases in 2022, translating to about 2.5 million new lung cancer cases [10] - In China, lung cancer represents about 22% of new cancer cases, with approximately 1.06 million new cases in 2022 [10] Section 2: Market Potential for Driver Gene-Negative NSCLC - The report highlights the significant market potential for immune therapies in treating driver gene-negative NSCLC, with a focus on the limitations of current treatment options [2][3] Section 3: Next-Generation Immunotherapy Approaches - The report discusses the advancements in dual (multi) antibody therapies and immune-oncology (IO) combined with antibody-drug conjugates (ADC), emphasizing their potential to improve treatment outcomes for patients with driver gene-negative NSCLC [5][8] - The clinical data supporting these new therapies is expected to catalyze further investment and development in this area [5] Section 4: Treatment Guidelines Comparison - The report compares treatment guidelines for driver gene-negative NSCLC between the United States and China, noting differences in treatment stratification and recommended therapies [32][34] - The U.S. guidelines emphasize PD-L1 expression levels, while Chinese guidelines focus more on performance status (PS) [32][34] Section 5: Future Catalysts - Key upcoming clinical data releases and studies are highlighted as potential catalysts for investment opportunities in the sector, particularly regarding dual antibodies and ADC therapies [5][8]
君实生物2月9日获融资买入2255.81万元,融资余额14.37亿元
Xin Lang Cai Jing· 2026-02-10 02:50
来源:新浪证券-红岸工作室 2月9日,君实生物涨1.43%,成交额2.61亿元。两融数据显示,当日君实生物获融资买入额2255.81万 元,融资偿还2816.42万元,融资净买入-560.61万元。截至2月9日,君实生物融资融券余额合计14.48亿 元。 融资方面,君实生物当日融资买入2255.81万元。当前融资余额14.37亿元,占流通市值的5.30%,融资 余额超过近一年90%分位水平,处于高位。 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90.67%,技术许可及特许权使用收入8.74%,技术服务及其他 0.59%。 截至9月30日,君实生物股东户数3.59万,较上期增加15.17%;人均流通股21361股,较上期减少 12.96%。2025年1月-9月,君实生物实现营业收入18.06亿元,同比增长42.06 ...