格隆汇12月18日丨君实生物(688180.SH)公布，公司于近日收到上海檀英出具的《关于君实生物减持计 划告知函》，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%。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》的减持政策：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。 ...

君实生物公告称，截至公告披露日，持股5.7914%的股东上海檀英，因基金期限与流动性资金安排，计 划在2026年1月13日至4月10日，通过大宗交易方式减持不超20,533,797股，即不超公司总股本2%。上海 檀英及一致行动人合计持股7.3263%，其在过去12个月内已减持公司1.1688%股份。本次减持计划存在 不确定性，但不会导致公司控制权变更，也不会对公司经营产生重大影响。 ...

证券日报网讯12月16日，乐普医疗（300003）在互动平台回答投资者提问时表示，截至目前，本公司及 关联方并未持有任何君实生物。 ...

Group 1 - The core viewpoint of the news is that Junshi Biosciences experienced a decline in stock price and significant trading activity, indicating potential investor concerns and market volatility [1] - On December 16, Junshi Biosciences' stock fell by 2.19%, with a trading volume of 197 million yuan, and a net financing outflow of 1.68 million yuan [1] - The total margin balance for Junshi Biosciences reached 1.377 billion yuan, with the financing balance accounting for 4.97% of the circulating market value, indicating a high level of leverage compared to the past year [1] Group 2 - Junshi Biosciences, established on December 27, 2012, focuses on the research and commercialization of monoclonal antibody drugs and other therapeutic protein drugs, with 90.67% of its revenue coming from drug sales [2] - For the period from January to September 2025, Junshi Biosciences reported a revenue of 1.806 billion yuan, representing a year-on-year growth of 42.06%, while the net profit attributable to shareholders was -596 million yuan, an increase of 35.72% year-on-year [2] - As of September 30, 2025, the number of shareholders increased by 15.17% to 35,900, while the average circulating shares per person decreased by 12.96% to 21,361 shares [2]

Core Viewpoint - The company, Junshi Biosciences, is focused on becoming a leading innovative pharmaceutical company with a complete industry chain capability, from drug discovery to commercialization, and is actively developing vaccines and monoclonal antibodies for various diseases, including monkeypox [2][3]. Company Overview - Junshi Biosciences was established on December 27, 2012, and went public on July 15, 2020. The company is headquartered in Shanghai and specializes in the research and commercialization of monoclonal antibodies and other therapeutic protein drugs [7]. - The main revenue sources for the company include drug sales (90.67%), technology licensing and royalties (8.74%), and technical services (0.59%) [7]. Financial Performance - For the period from January to September 2025, Junshi Biosciences reported a revenue of 1.806 billion yuan, representing a year-on-year growth of 42.06%. However, the net profit attributable to the parent company was -596 million yuan, which is a 35.72% increase compared to the previous year [8]. Product Development - The company has developed a comprehensive pipeline of innovative drugs, including the first domestically approved PD-1 monoclonal antibody, Toripalimab, which has received approval for 11 indications in mainland China and is also approved in multiple countries including the US and EU [2]. - Junshi Biosciences is also developing Tifcemalimab, the world's first anti-BTLA monoclonal antibody, which is currently in Phase III clinical trials [2]. Collaborations and Research - On October 27, 2023, Junshi Biosciences announced collaborations with several research institutions and universities to develop a recombinant protein vaccine for monkeypox, with related products currently in preclinical development [3].

Core Viewpoint - The company Junshi Biosciences (01877.HK) has received approval from the U.S. Food and Drug Administration (FDA) for its clinical trial application of the EGFR/HER3 bispecific antibody-drug conjugate (code: JS212) for the treatment of advanced solid tumors [1] Group 1 - The FDA notification indicates a significant milestone for the company in advancing its oncology pipeline [1] - The approval allows the company to proceed with clinical trials, which could lead to potential market opportunities if successful [1]

2025年1月，JS212的临床试验申请获得国家药品监督管理局(国家药监局)受理，并于2025年3月获得国 家药监局批准。截至本公告日期，JS212正在中国内地开展一项开放标签、剂量递增和剂量扩展的I/II期 临床试验，旨在晚期实体瘤患者中评估JS212的安全性、耐受性、药代动力学和初步疗效。此外，JS212 多队列联合用药的临床试验申请已于2025年11月获得国家药监局批准，计划于近期开展相关临床研究。 本文源自：智通财经网 消息面上，12月14日，君实生物发布公告，本公司收到美国食品药品监督管理局(FDA)的通知， EGFR/HER3双特异性抗体偶联药物(代号：JS212)用于治疗晚期实体瘤的临床试验申请获得FDA批准。 智通财经获悉，君实生物(01877)涨超4%，截至发稿，涨4.33%，报25港元，成交额3483.03万港元。 ...

Core Viewpoint - Multiple pharmaceutical companies announced positive developments, including FDA approvals and clinical trial advancements, indicating a favorable environment for the sector. Group 1: FDA Approvals and Clinical Trials - Ji'an Medical announced that its U.S. subsidiary received pre-market notification from the FDA for its quadrivalent home test kits for influenza A, influenza B, COVID-19, and RSV, allowing for normal sales in the U.S. market [1] - Junshi Biosciences reported that its EGFR/HER3 bispecific antibody-drug conjugate for treating advanced solid tumors received FDA approval for clinical trial application [1] - Innovent Biologics disclosed that its self-developed BTK inhibitor, Orelabrutinib, achieved the primary endpoint in a Phase II study for systemic lupus erythematosus and has been approved for Phase III registration clinical trials [1] Group 2: Strategic Partnerships and Product Developments - Yipinhong announced that its Qinxing Qingjie oral solution was approved as a national second-level protected traditional Chinese medicine. Additionally, the company secured a deal with Swedish pharmaceutical giant Sobi for $950 million (approximately 6.713 billion RMB) upfront and up to $550 million (approximately 3.887 billion RMB) in additional payments for a new URAT1 inhibitor, which has shown strong efficacy in dissolving gout stones and has received FDA fast track designation, with key Phase III clinical trials completed [1]

每经AI快讯，君实生物(01877.HK)涨超4%，截至发稿涨4.33%，报25港元，成交额3483.03万港元。 ...

智通财经APP获悉，君实生物(01877)涨超4%，截至发稿，涨4.33%，报25港元，成交额3483.03万港 元。 2025年1月，JS212的临床试验申请获得国家药品监督管理局(国家药监局)受理，并于2025年3月获得国 家药监局批准。截至本公告日期，JS212正在中国内地开展一项开放标签、剂量递增和剂量扩展的I/II期 临床试验，旨在晚期实体瘤患者中评估JS212的安全性、耐受性、药代动力学和初步疗效。此外，JS212 多队列联合用药的临床试验申请已于2025年11月获得国家药监局批准，计划于近期开展相关临床研究。 消息面上，12月14日，君实生物发布公告，本公司收到美国食品药品监督管理局(FDA)的通知， EGFR/HER3双特异性抗体偶联药物(代号：JS212)用于治疗晚期实体瘤的临床试验申请获得FDA批准。 ...