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9月22日晚间重要公告一览
Xi Niu Cai Jing· 2025-09-22 11:58
Group 1 - Xinxiang Chemical Fiber will suspend production for approximately 90 days starting October 1, 2025, affecting an annual capacity of 31,200 tons, resulting in a revenue decrease of approximately 185 million yuan and a profit reduction of about 48 million yuan [1] - Bozhong Precision plans to transfer 18.29% of its stake in Suzhou Linghou Robot for 64 million yuan, retaining a 21.61% ownership post-transaction [1] - Haixing Electric is a recommended candidate for a State Grid procurement project, with an expected bid amount of approximately 128 million yuan [2] Group 2 - Samsung Medical is a recommended candidate for multiple State Grid procurement projects, with a total expected bid amount of approximately 193 million yuan [2][3] - Youxunda is a recommended candidate for a State Grid procurement project, with a bid amount of approximately 107 million yuan, representing 10.55% of its 2024 revenue [3] - Tiancheng Self-Control has received a notification for a seat assembly project from a well-known domestic new energy vehicle company, expected to start mass production in June 2026 [4] Group 3 - YKYY013 injection has received FDA approval for clinical trials to treat chronic hepatitis B virus infection [4] - Pulaide has signed a strategic cooperation agreement with an international electric tool brand, with a total procurement amount exceeding 700 million yuan over five years [4] - Sichuan Shuangma's subsidiary has obtained GMP certification from Russia, covering core aspects of drug quality and production systems [6] Group 4 - Boshi Co. has signed an industrial service contract worth approximately 96.99 million yuan with Guoneng Baotou Coal Chemical [7] - Wansheng Intelligent is a recommended candidate for a State Grid project, with an expected bid amount of approximately 67.98 million yuan, representing 7.25% of its 2024 revenue [9][10] - Huazi Industrial plans to sell its dairy farm assets for 38.5 million yuan, expecting a positive impact of approximately 11.7 million yuan on its current profits [10] Group 5 - Jinguang Electric has won a State Grid project with a total bid amount of approximately 28.4 million yuan, accounting for 3.82% of its 2024 revenue [11] - Nanjiao Food reported a net profit of 10,410 yuan for August, a year-on-year decrease of 98.31% [13] - Dongfang Bio's subsidiary has obtained registration certificates for two medical device products [15] Group 6 - Lanhua Kecai has signed a strategic cooperation agreement with Shanghai Pangu Power to promote intelligent and efficient transformation in the coal mining industry [17] - Yabao Pharmaceutical has decided to terminate the SY-009 research project, with a total investment of approximately 87.87 million yuan to be fully impaired [18] - Tian Shili's subsidiary has received approval for a new indication for its recombinant human urokinase injection for acute ischemic stroke treatment [20] Group 7 - Su Yan Jingshen's executives plan to increase their shareholding in the company, with a total investment of between 1.9 million and 2.66 million yuan [22] - Baiyun Electric and its subsidiary have won a State Grid project with a total bid amount of approximately 162 million yuan, covering multiple equipment types [23] - China West Electric's director has resigned due to work reasons, effective September 19, 2025 [25] Group 8 - Jianan Intelligent is a recommended candidate for a State Grid project with a total expected bid amount of approximately 73.12 million yuan [26] - Juhua Technology is a recommended candidate for a State Grid project with a total expected bid amount of approximately 142 million yuan [27] - Tengyuan Cobalt's actual controller has committed not to reduce holdings for the next 12 months, holding 37.89% of the total shares [28] Group 9 - Changfei Optical Fiber announced that Draka Comteq B.V. no longer holds H shares in the company after selling 37.59 million shares [28] - Mongcao Ecological's subsidiary has signed a contract for an ecological restoration project worth 225.2 million yuan [29] - Weiao Co. plans to distribute a cash dividend of 0.1 yuan per share, totaling approximately 39.29 million yuan [30]
天士力加入生物创新药国家队 普佑克脑梗适应症获批
Group 1 - The domestic innovative drug industry is experiencing unprecedented development opportunities, with the number of approved innovative drugs reaching a five-year high in the first half of this year [1] - The State-owned Assets Supervision and Administration Commission has indicated that the government is preparing to create a national team for biomedicine [1] - Tian Shi Li's innovative drug, Pu You Ke, has received approval for a new indication for the treatment of acute ischemic stroke (AIS) [1][4] Group 2 - Pu You Ke is recognized as a safe thrombolytic drug by the prestigious medical journal The Lancet Neurology, and it has a unique thrombolytic mechanism with a low risk of systemic bleeding [1][2] - Clinical trials have shown that Pu You Ke significantly reduces the incidence of symptomatic intracranial hemorrhage compared to control groups [2][4] - The drug is effective in improving neurological function and quality of life for AIS patients when administered within 4.5 hours of symptom onset [4] Group 3 - Tian Shi Li has undergone a change in controlling shareholder to China Resources Sanjiu, positioning itself as a member of the China Resources group [5] - The company aims to become a leading innovative pharmaceutical enterprise in China, focusing on innovation-driven strategies [5][6] - Tian Shi Li has a pipeline of 31 innovative drugs in development, including several high-profile CGT and antibody drugs [5][6] Group 4 - The company is transitioning from a traditional pharmaceutical enterprise to an innovative pharmaceutical company, leveraging the support of the China Resources system [6] - The approval of Pu You Ke for the AIS indication demonstrates Tian Shi Li's accumulated experience and capability in biopharmaceutical innovation [6] - The market has not fully priced in the value of Tian Shi Li's innovative biopharmaceutical pipeline, indicating potential for value re-evaluation [6]
天士力注射用重组人尿激酶原增加急性缺血性脑卒中新适应症获批
Bei Jing Shang Bao· 2025-09-22 09:27
Core Viewpoint - Tianjin Tasly Pharmaceutical has received approval from the National Medical Products Administration for its innovative drug, recombinant human urokinase (Puyouke), to be used for thrombolytic treatment of acute ischemic stroke, marking its second approved indication in China [1] Group 1 - The drug Puyouke was developed under the "Major New Drug Creation" project supported by the national "11th Five-Year Plan" and is classified as a Class 1 biological innovative drug [1] - The newly approved indication for acute ischemic stroke expands the therapeutic applications of Puyouke, which was previously approved for acute ST-segment elevation myocardial infarction [1]
天士力:注射用重组人尿激酶原新适应症获药品注册证书
Core Viewpoint - Tianjin Tasly Pharmaceutical Co., Ltd. has received approval from the National Medical Products Administration for its innovative drug, recombinant human urokinase (Puyouke), to be used for thrombolytic treatment of acute ischemic stroke, marking its second approved indication in China [1] Group 1 - The drug Puyouke was initially approved for acute ST-segment elevation myocardial infarction during the "11th Five-Year Plan" under a major national project for new drug development [1] - The newly approved indication for acute ischemic stroke expands the therapeutic applications of Puyouke, enhancing its market potential [1]
国内首个双试验证实!天士力“降茶”以医学级消费品开辟无糖茶功能新赛道
Xin Hua Cai Jing· 2025-09-22 08:45
Core Insights - Tianshili's "Jiangcha" has released the first human clinical trial report for sugar-free tea in China, marking a significant step from conceptual consumption to scientific and standardized development in the sugar-free tea beverage sector [2][4] - The company has filled a research gap in the domestic market by completing a scientific validation process for sugar-free tea, which has been lacking in evidence-based research and standardized verification compared to Japan [3][4] Research and Development - Tianshili's "Jiangcha" has successfully completed both animal and human clinical trials, establishing a complete scientific loop from basic experiments to clinical validation, thus filling a research void in the field [4][9] - The animal trials involved a 16-week study on male SD rats, using a high-fructose high-fat diet to induce metabolic syndrome, with various intervention groups to assess the effects of tea polyphenols [5][6] Clinical Trial Results - The human clinical trial was designed as a randomized, open-label, controlled study with 72 participants, showing significant improvements in blood sugar and lipid levels after consuming high doses of tea polyphenols [7][12] - Results indicated that the "Jiangcha" group had statistically significant lower postprandial blood sugar levels compared to the control group, confirming its effectiveness in inhibiting post-meal blood sugar spikes [12] Key Ingredients - The core component of Tianshili's "Jiangcha" is tea polyphenols, which have been recognized for their role in regulating sugar and lipid metabolism, improving gut microbiota, and maintaining overall health [13] - Recent studies have highlighted the mechanisms through which tea polyphenols exert their effects, including modulation of gut microbiota and activation of specific metabolic pathways [13] Future Directions - Tianshili aims to continue its research on sugar and lipid metabolism, focusing on the development of health products based on evidence and scientific validation [15] - The company is committed to leveraging its extensive pharmaceutical research experience to innovate in the health product sector, aspiring to become a leader in the global market for sugar and lipid metabolism management [15]
天士力:全资子公司药品普佑克新增适应症获批
Xin Lang Cai Jing· 2025-09-22 08:34
Core Viewpoint - Tianjin Tasly Pharmaceutical has received approval from the National Medical Products Administration for its recombinant human urokinase (brand name: Puyouke) to be used for thrombolytic treatment of acute ischemic stroke, expanding its product line in the neurology/psychiatry sector [1] Group 1 - The product Puyouke is currently the only approved recombinant human urokinase product in China [1] - Puyouke is the first Class 1 biological innovative drug supported by the "Major New Drug Creation" technology major project during the "11th Five-Year Plan" period [1] - The drug is already approved for the treatment of acute ST-segment elevation myocardial infarction, and the new indication enhances the company's offerings in the neurological field [1]
天士力(600535) - 天士力关于全资子公司注射用重组人尿激酶原增加急性缺血性脑卒中新适应症获得药品注册证书的公告
2025-09-22 08:30
证券代码:600535 证券简称:天士力 编号:临 2025-064 号 天士力医药集团股份有限公司 关于全资子公司注射用重组人尿激酶原增加急性缺血性脑卒中 新适应症获得药品注册证书的公告 药品名称:注射用重组人尿激酶原(商品名称:普佑克) 剂型:注射剂 规格:5mg(50 万 IU)/支 申请事项:新增急性缺血性脑卒中的溶栓治疗适应症 受理号:CXSS2400083 通知书编号:2025S02596 注册分类:治疗用生物制品 药品批准文号:国药准字 S20110003 本公司董事会及全体董事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、准确性和完整性承担个别及连带责任。 近日,天士力医药集团股份有限公司(以下简称"公司")全资子公司天士 力生物医药股份有限公司(以下简称"天士力生物")收到国家药品监督管理局 核准签发的《药品注册证书》,批准公司拥有自主知识产权的生物创新药注射用 重组人尿激酶原(普佑克)新增适应症,用于急性缺血性脑卒中的溶栓治疗。普 佑克是"十一五"规划期间国家"重大新药创制"科技重大专项支持下获批的 1 类生物创新药(急性 ST 段抬高型心肌梗死适应症), ...
天士力(600535.SH)子公司注射用重组人尿激酶原增加急性缺血性脑卒中新适应症获药品注册证书
智通财经网· 2025-09-22 08:29
Core Viewpoint - Tianjin Tasly Pharmaceutical Co., Ltd. has received approval from the National Medical Products Administration for its innovative drug, recombinant human urokinase (Puyouke), to be used for thrombolytic treatment of acute ischemic stroke, expanding its market potential and product line in the neurology/psychiatry sector [1] Group 1 - The company’s subsidiary, Tasly Biopharmaceuticals, has been granted a drug registration certificate for Puyouke, which now has a new indication for acute ischemic stroke [1] - Puyouke is the only approved recombinant human urokinase product in China and is the first class of innovative biological drug supported by the national "Major New Drug Creation" project during the "11th Five-Year Plan" [1] - The approval of the new indication enhances the company's product offerings and competitiveness in the market by targeting a broader patient population [1]
天士力(600535.SH):子公司注射用重组人尿激酶原增加急性缺血性脑卒中新适应症获得药品注册证书
Ge Long Hui A P P· 2025-09-22 08:27
Core Viewpoint - Tianjin Tasly Pharmaceutical Co., Ltd. (600535.SH) announced that its wholly-owned subsidiary, Tasly Biopharmaceuticals Co., Ltd., received approval from the National Medical Products Administration for a new indication of its innovative biological drug, Recombinant Human Urokinase (Puyouke), for thrombolytic treatment of acute ischemic stroke [1] Group 1 - The drug Puyouke is a Class 1 innovative biological drug that was supported by the "Major New Drug Creation" technology major project during the "Eleventh Five-Year Plan" period [1] - This new indication for acute ischemic stroke is the second approved indication for the drug in China, following its initial approval for acute ST-segment elevation myocardial infarction [1]
天士力子公司注射用重组人尿激酶原增加急性缺血性脑卒中新适应症获药品注册证书
Zhi Tong Cai Jing· 2025-09-22 08:24
普佑克作为国内目前唯一获批上市的重组人尿激酶原产品,也是首个获批"十一五"规划期间国家"重大 新药创制"科技重大专项支持下的1类生物创新药。该药已上市适应症为急性ST段抬高型心肌梗死,本 次新增急性缺血性脑卒中溶栓治疗适应症的获批丰富了公司神经/精神领域产品线,进一步拓展了产品 目标患者人群,有利于提升公司及产品市场竞争力。 天士力(600535)(600535.SH)发布公告,近日,公司全资子公司天士力生物医药股份有限公司(简称"天 士力生物")收到国家药品监督管理局核准签发的《药品注册证书》,批准公司拥有自主知识产权的生物 创新药注射用重组人尿激酶原(普佑克)新增适应症,用于急性缺血性脑卒中的溶栓治疗。普佑克是"十 一五"规划期间国家"重大新药创制"科技重大专项支持下获批的1类生物创新药(急性ST段抬高型心肌梗 死适应症),本次急性缺血性脑卒中适应症是该药在国内获批的第二个适应症。 ...