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研报掘金丨开源证券:维持天士力“买入”评级,普佑克斩获AIS溶栓新适应症
Ge Long Hui A P P· 2025-09-23 08:46
Core Viewpoint - The report from Open Source Securities highlights that Tianshili has announced a new indication for its proprietary biological innovative drug, Recombinant Human Urokinase (Puyouke), for thrombolytic treatment of acute ischemic stroke, marking its second approved indication in China [1] Group 1: Product Development - Puyouke was approved as a Class 1 biological innovative drug during the "11th Five-Year Plan" under the national "Major New Drug Creation" technology major project, initially for acute ST-segment elevation myocardial infarction [1] - The new indication for acute ischemic stroke is expected to enhance the drug's market potential and reflects the company's strategic focus on expanding its product offerings [1] Group 2: Financial Projections - The company maintains its profit forecasts for the years 2025 to 2027, estimating net profits of 1.183 billion, 1.306 billion, and 1.455 billion yuan respectively [1] - Earnings per share (EPS) are projected to be 0.79, 0.87, and 0.97 yuan per share for the same years, with corresponding price-to-earnings (PE) ratios of 19.8, 18.0, and 16.1 times [1] Group 3: Investment Rating - The report maintains a "Buy" rating for the stock, indicating confidence in the company's growth potential driven by the dual indications of Puyouke [1]
国产生物创新药再获突破 天士力普佑克获批用于急性脑梗治疗
Xin Hua Cai Jing· 2025-09-23 08:26
Core Viewpoint - The approval of the innovative drug "普佑克" (recombinant human urokinase) for treating acute ischemic stroke (AIS) marks a significant breakthrough in China's thrombolytic therapy for stroke, reflecting the country's push for innovation in biomedicine [1][2]. Company Summary - Tian Shi Li Pharmaceutical Group has received approval from the National Medical Products Administration for its innovative drug "普佑克," which is now indicated for AIS treatment, following its previous approval for acute ST-segment elevation myocardial infarction [1]. - The drug has demonstrated a lower risk of bleeding compared to competitors, as evidenced by clinical trials published in reputable medical journals [1]. - The company has 31 innovative drug projects in development, including advancements in cell and gene therapy and bispecific antibodies, with three products recently receiving clinical approval [2]. Industry Summary - The biopharmaceutical industry in China is experiencing unprecedented growth, with a 59% year-on-year increase in the number of innovative drugs approved in the first half of 2025, totaling 43 approvals, of which 93% are domestic innovations [3]. - The integration of Tian Shi Li into China Resources Sanjiu is expected to enhance its capabilities in key therapeutic areas, optimizing its research and development pipeline [3]. - The Chinese government has implemented supportive policies for the development of innovative drugs, creating a favorable environment for the biopharmaceutical sector [3].
天士力: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
Zheng Quan Ri Bao Wang· 2025-09-23 07:13
Core Viewpoint - Tianjin Tasly Pharmaceutical Co., Ltd. announced the approval of a new indication for its innovative biological drug, recombinant human urokinase (Puyouke), for thrombolytic treatment of acute ischemic stroke by the National Medical Products Administration [1] Group 1 - The company received a drug registration certificate for the new indication [1] - The drug has independent intellectual property rights [1] - The new application is specifically for the treatment of acute ischemic stroke [1]
天士力(600535):普佑克新适应症获批,有望打造第二成长曲线
Xinda Securities· 2025-09-23 07:04
Investment Rating - The report assigns a "Buy" rating for the stock of Tian Shili (600535) based on its potential growth from the newly approved indication for its drug, Pu You Ke [1]. Core Viewpoints - The approval of Pu You Ke for the treatment of acute ischemic stroke is expected to create a second growth curve for the company, leveraging its established commercial framework and clinical evidence [2][3]. - Acute ischemic stroke has a high incidence rate, and Pu You Ke is positioned to meet unmet clinical needs, offering a safer alternative to existing treatments like alteplase [4][5][6]. - The company is committed to innovation, with a robust pipeline of 83 projects, including several promising drugs that could enhance its market position [7][8]. Financial Summary - The projected revenue for the company from 2025 to 2027 is expected to be 86.60 billion, 93.24 billion, and 100.81 billion respectively, with net profits of 11.96 billion, 13.31 billion, and 14.84 billion [10]. - The earnings per share (EPS) are forecasted to be 0.80 yuan, 0.89 yuan, and 0.99 yuan for the same period, with corresponding price-to-earnings (P/E) ratios of 19.62, 17.63, and 15.82 [10].
13只股中线走稳 站上半年线
Core Viewpoint - The Shanghai Composite Index is currently above the six-month moving average, with a slight decline of 1.04% and a total trading volume of 1.262 trillion yuan [1] Group 1: Market Performance - As of 10:29 AM today, the Shanghai Composite Index stands at 3788.76 points, indicating a trading volume of 12,621.13 million yuan [1] - There are 13 A-shares that have surpassed the six-month moving average today, with notable stocks including Air China Ocean, Guisheng Co., and Samsung Medical, showing divergence rates of 4.09%, 2.35%, and 1.79% respectively [1] Group 2: Individual Stock Analysis - The top three stocks with the highest divergence rates are: - Air China Ocean (Code: 833171) with a price increase of 4.78%, a turnover rate of 10.78%, a six-month moving average of 10.52 yuan, and a latest price of 10.95 yuan, resulting in a divergence rate of 4.09% [1] - Guisheng Co. (Code: 600992) with a price increase of 4.08%, a turnover rate of 5.15%, a six-month moving average of 14.45 yuan, and a latest price of 14.79 yuan, resulting in a divergence rate of 2.35% [1] - Samsung Medical (Code: 601567) with a price increase of 4.73%, a turnover rate of 2.47%, a six-month moving average of 23.27 yuan, and a latest price of 23.69 yuan, resulting in a divergence rate of 1.79% [1]
天士力生物创新药重磅突破,普佑克脑梗适应症获批
Group 1: Product and Market Potential - Puyouke is a first-class biological innovative drug approved under the "Major New Drug Creation" project, now gaining approval for acute ischemic stroke indication, marking its second indication in China [1] - Compared to other thrombolytic drugs, Puyouke has a unique thrombolytic mechanism with lower systemic bleeding risk and high safety, showing a significantly lower rate of symptomatic intracranial hemorrhage in clinical trials [1] - In 2019, there were 3.94 million new stroke cases in China, with ischemic strokes accounting for 2.87 million (72.8%), indicating a growing market for stroke treatment [2] Group 2: Industry Trends and Treatment Rates - The incidence of ischemic stroke in China increased from 117 per 100,000 in 2005 to 145 per 100,000 in 2019, with an annual growth rate of 4-6% [2] - The treatment rates for acute ischemic stroke in China are still low, with intravenous thrombolysis at 5.64% and endovascular treatment at only 1.45% in 2019-2020, suggesting significant room for improvement [2] Group 3: Company Innovation and Pipeline - Tianshili is focused on dual-engine innovation in traditional Chinese medicine and biological drugs, with 31 innovative drugs in its pipeline [3] - The company has made significant progress in both traditional and biological drug sectors, with multiple products in late-stage clinical trials [3] - Following its integration with China Resources Sanjiu, Tianshili aims to become a leading innovative pharmaceutical company in China, with a clear strategy for its research pipeline that has yet to be fully valued by the market [3]
天士力(600535):普佑克斩获AIS溶栓新适应症,核心单品价值凸显
KAIYUAN SECURITIES· 2025-09-23 01:42
Investment Rating - The investment rating for the company is "Buy" (maintained) [1] Core Views - The company announced the approval of a new indication for its innovative drug, Puyouke, for thrombolytic treatment of acute ischemic stroke, enhancing its product portfolio and long-term growth potential [4][6] - The company is expected to maintain its net profit forecasts for 2025-2027 at 1.183 billion, 1.306 billion, and 1.455 billion yuan respectively, with corresponding EPS of 0.79, 0.87, and 0.97 yuan per share [4][7] - The current stock price corresponds to P/E ratios of 19.8, 18.0, and 16.1 for the years 2025, 2026, and 2027 respectively [4][7] Financial Summary - Revenue for 2023 is reported at 8.674 billion yuan, with a slight decrease expected in 2024 to 8.498 billion yuan, followed by a recovery to 8.827 billion yuan in 2025 [7][9] - The gross margin is projected to remain stable around 67% from 2025 to 2027, while the net profit margin is expected to improve from 13.4% in 2025 to 14.6% in 2027 [7][10] - The return on equity (ROE) is forecasted to increase from 9.3% in 2025 to 9.5% in 2027 [7][10]
中纪委推进医药领域纠风治乱;体外类胃囊模型构建成功
Policy Developments - The Central Commission for Discipline Inspection and the National Supervisory Commission are intensifying efforts to rectify issues in the pharmaceutical sector, focusing on eliminating practices such as medical staff accepting "red envelopes" and improper benefits through academic exchanges [1] Drug and Device Approvals - YKYY013 injection from Yuyuan Pharmaceutical has received FDA approval for clinical trials aimed at treating chronic hepatitis B virus infection, which utilizes a dual-stranded siRNA mechanism to silence the virus [2] - *ST Suwu's hydrochloride lincomycin injection has passed the consistency evaluation for generic drugs, receiving approval from the National Medical Products Administration [3] - Tianjin Pharmaceutical's recombinant human urokinase (Puyouke) has been granted approval for a new indication for thrombolytic treatment of acute ischemic stroke, expanding its product line in the neurological field [4] Capital Market - Lepu Medical has entered into a strategic cooperation agreement with Hanhai Information Technology, aiming to enhance its medical aesthetics business through shared resources and a comprehensive sales network [5] Industry Events - The National Medical Insurance Administration has published the first batch of typical cases involving violations by designated medical institutions, highlighting issues such as falsifying medical records and duplicate charges [6] - Starting January 1, 2025, a new management system for medical insurance payment qualifications will be implemented, introducing a point-based system for violations to ensure the safety of medical insurance funds [7] Research and Development - Researchers at Kunming University of Science and Technology have successfully constructed an in vitro model of the stomach, providing a new platform for studying human gastric organ development [8] Public Sentiment Alerts - Zhejiang Pharmaceutical announced that its shareholder, Guotou Gaoke, plans to reduce its stake by up to 1% within three months, which will not affect the company's control [9]
华东医药ADC创新药临床试验获FDA批准;亚宝药业终止一药品研发
Mei Ri Jing Ji Xin Wen· 2025-09-22 23:17
Group 1: Huadong Medicine - Huadong Medicine's subsidiary received FDA approval for the clinical trial of HDM2017, a new antibody-drug conjugate targeting Cadherin17 for advanced malignant solid tumors [1] Group 2: Tianjin Tasly - Tasly's subsidiary received approval for the new indication of Pu You Ke for thrombolytic treatment of acute ischemic stroke, making it the only approved recombinant human urokinase product in China [2] Group 3: Yabao Pharmaceutical - Yabao Pharmaceutical decided to terminate the clinical trial of SY-009 and fully provision for asset impairment of 55.793 million yuan, which will reduce the company's profit for 2025 [3][4] Group 4: Zhixiang Jintai - Zhixiang Jintai signed exclusive cooperation agreements with Kangzhe Pharmaceutical for the commercialization of GR2001 and GR1801 monoclonal antibodies, with expected payments totaling approximately 510 million yuan [4] Group 5: Lepu Medical - Lepu Medical entered a strategic partnership with Hanhai Information to jointly develop the medical aesthetics business, aiming to enhance sales channels and improve performance amid industry competition [5]
华东医药ADC创新药临床试验获FDA批准;亚宝药业终止一药品研发丨医药早参
Mei Ri Jing Ji Xin Wen· 2025-09-22 23:12
Group 1 - Huadong Medicine's subsidiary received FDA approval for the clinical trial of HDM2017, a new antibody-drug conjugate targeting Cadherin 17, for advanced malignant solid tumors [1] - Tianjin Pharmaceutical's subsidiary obtained approval for the new indication of Pu You Ke for thrombolytic treatment of acute ischemic stroke, making it the only approved recombinant human urokinase product in China [2] - Yabao Pharmaceutical decided to terminate the clinical trial of SY-009 and fully provision for asset impairment of 55.793 million yuan, which will reduce the company's profit for 2025 [3] Group 2 - Zhixiang Jintai signed exclusive cooperation agreements with Kangzhe Pharmaceutical for the commercialization of GR2001 and GR1801 monoclonal antibodies, with expected payments totaling approximately 510 million yuan [4] - Lepu Medical established a strategic partnership with Hanhai Information to jointly develop the medical aesthetics business, aiming to enhance sales channels and improve performance amid industry competition [5][6]