证券代码：300573 证券简称：兴齐眼药 公告编号：2025-053 沈阳兴齐眼药股份有限公司 关于完成工商变更登记的公告 本公司及董事会全体成员保证信息披露内容的真实、准确、完整，没有 虚假记载、误导性陈述或重大遗漏。 沈阳兴齐眼药股份有限公司（以下简称"公司"）第五届董事会第十次会议 及2025年第二次临时股东大会审议通过了《关于变更公司注册资本并修订<公司 章程>的议案》。具体内容详见《关于变更公司注册资本并修订<公司章程>的公告》 （公告编号：2025-040）及《2025年第二次临时股东大会决议公告》（公告编号： 2025-042）。 公司于近日完成了工商变更登记及备案手续，并取得了沈阳市浑南区市场监 督管理局颁发的《营业执照》，具体信息如下： 1、统一社会信用代码：912101001179988209 2、名称：沈阳兴齐眼药股份有限公司 3、类型：股份有限公司 4、法定代表人：刘继东 5、经营范围：许可项目：药品生产，保健食品生产，消毒剂生产（不含危 险化学品），检验检测服务，药品进出口（依法须经批准的项目，经相关部门批 准后方可开展经营活动，具体经营项目以审批结果为准）一般项目：塑料制品制 造 ...

Core Insights - Over 170 pharmaceutical and biotechnology companies have been investigated by institutions since September, with a focus on innovative drug companies like Maiwei Biotech and Ganli Pharmaceutical, highlighting the importance of R&D investment and business development transactions [1][2] Group 1: Company Research and Development - Maiwei Biotech has received the highest institutional attention, with over 330 institutional investigations, and recently signed exclusive licensing and preferred stock purchase agreements for the 2MW7141 project [2] - Ganli Pharmaceutical aims to become a large multinational pharmaceutical company and has been investing in innovative drug development for about a decade, focusing on technologies like PROTAC and ADC [2] - Xingqi Eye Pharmaceutical has completed Phase I clinical trials for its SQ-22031 eye drops and is conducting Phase II trials for neurotrophic keratitis [3] Group 2: AI Applications in Pharmaceuticals - Xiangsheng Medical is integrating AI and robotics in ultrasound technology to enhance cancer screening capabilities [4] - Haoyuan Pharmaceutical is developing an AI-driven drug screening platform and aims to improve operational efficiency through AI applications in drug development [4][5] - Enhua Pharmaceutical is exploring the use of AI in early-stage drug development and plans to establish a system for this purpose [5] Group 3: Industry Trends and Future Outlook - The innovative drug sector is expected to maintain a high level of activity, with a focus on the upcoming 2025 European Society for Medical Oncology (ESMO) conference and related clinical data disclosures [6] - The Chinese pharmaceutical industry has transitioned to a new growth model, with traditional companies like Heng Rui and Han Sen successfully pivoting to innovation [6] - The trend of "innovation + internationalization" remains a core direction for the pharmaceutical sector, with ongoing policy support expected to enhance the global competitiveness of domestic innovative drug companies [6]

Core Insights - Over 170 pharmaceutical and biotechnology companies have been investigated by institutions since September, with a focus on innovative drug companies like Maiwei Biotech and Ganli Pharmaceutical, highlighting the trend of "innovation + internationalization" in the industry [1][6] Group 1: Company Research and Development - Maiwei Biotech has received the highest institutional attention, with over 330 institutional investigations, and recently signed exclusive licensing and preferred stock purchase agreements for the 2MW7141 project [2] - Ganli Pharmaceutical aims to become a large multinational pharmaceutical company and has been investing in innovative drug development for about a decade, focusing on technologies like PROTAC and ADC [2] - Xingqi Eye Medicine has completed Phase I clinical trials for its SQ-22031 eye drops and is conducting Phase II trials for neurotrophic keratitis [3] Group 2: AI Applications in Pharmaceuticals - Xiangsheng Medical is integrating AI and robotics in ultrasound technology to enhance cancer screening capabilities [4] - Haoyuan Pharmaceutical is developing an AI-driven drug screening platform and aims to improve operational efficiency through AI applications in drug development [4][5] - Enhua Pharmaceutical is exploring the use of AI in early-stage drug development and plans to establish a system for this purpose [5] Group 3: Market Outlook and Trends - The innovative drug sector is expected to maintain a high level of activity, with significant opportunities arising from clinical data disclosures and business development transactions around the 2025 ESMO conference [6] - The Chinese pharmaceutical industry has transitioned to a new growth model, with traditional companies like Heng Rui and Han Sen successfully pivoting to innovation [6] - The trend of "innovation + internationalization" remains a core direction for the pharmaceutical sector, with ongoing policy support expected to enhance the global competitiveness of domestic innovative drug companies [6]

Core Viewpoint - Xingqi Eye Pharmaceutical has received clinical trial approval for SQ-129 vitreous sustained-release injection, aimed at treating diabetic macular edema and macular edema caused by retinal vein occlusion, indicating potential for market entry as no similar products are currently approved in China [1][2]. Group 1: Product Development - SQ-129 is classified as a Class 2 modified new chemical drug, demonstrating good safety and clinical development value based on extensive research [1]. - The company has established a comprehensive product system covering ten categories of ophthalmic drugs, including treatments for myopia, dry eye, and infections [2]. - The R&D center has developed seven technical platforms and various evaluation technologies, enhancing the company's ability to convert technical achievements into marketable products [2]. Group 2: Clinical Trials and Approvals - As of mid-2025, the company has made significant progress in clinical trials, with multiple products at various stages, including the completion of Phase I trials for voriconazole eye drops and the initiation of Phase III trials for lidocaine eye gel [3]. - SQ-22031 eye drops have also progressed to Phase II trials for neurotrophic keratitis, which was included in China's rare disease list in 2023 [3]. Group 3: Market Position and Strategy - The company focuses on the high-tech, high-risk, and high-value characteristics of pharmaceutical products, emphasizing the long and complex process from clinical trials to market launch [2]. - Xingqi Eye Pharmaceutical is committed to actively advancing its R&D projects in compliance with national regulations and will disclose information based on development progress [2].

Group 1 - Jinli Permanent Magnet expects a net profit of 505 million to 550 million yuan for the first three quarters of 2025, representing a year-on-year increase of 157% to 179% [1] - Guangdong Mingzhu anticipates a net profit of 215 million to 263 million yuan for the first three quarters of 2025, with a year-on-year growth of 858.45% to 1,071.44% [1] - Guangda Special Materials forecasts a net profit of approximately 248 million yuan for the first three quarters of 2025, reflecting a year-on-year increase of about 213.92% [2] Group 2 - Taotao Vehicle expects a net profit of 580 million to 620 million yuan for the first three quarters of 2025, indicating a year-on-year growth of 92.46% to 105.73% [2] - Dongfang Wealth has set the initial transfer price at 24.40 yuan per share, which is an 8.9% discount from the closing price [3] - Ganfeng Lithium has established a complete integrated layout for solid-state batteries and possesses commercialization capabilities [3] Group 3 - Huahai Pharmaceutical's subsidiary has received acceptance for the marketing authorization application of a targeted IL-36R antibody, which is the first of its kind developed in China [4][5] - Xingqi Eye Medicine has obtained clinical trial approval for SQ-129, a sustained-release injection for treating diabetic macular edema [6] - Muyuan Foods has raised its forecast for piglet output in 2025 to a range of 12 million to 14.5 million heads [6] Group 4 - Tianhe Magnetic Materials plans to invest 900 million yuan in high-performance rare earth permanent magnet projects [6] - Qianli Technology reported a significant increase in new energy vehicle production, with 4,282 units produced in September 2025, a year-on-year increase of 975.88% [6] - Yongzhen Co. has signed a strategic cooperation agreement with BYD to provide aluminum alloy components for energy storage [6] Group 5 - Xingye Silver Tin's controlling shareholder has completed its restructuring plan without changing the control of the listed company [7] - Jiangxi Copper has experienced significant price increases in its main products, copper cathodes and gold [7] - Saisir has signed a framework agreement with ByteDance's Volcano Engine for collaboration in embodied intelligence [8] Group 6 - Luoyang Molybdenum's production and operational activities remain normal, with no significant fluctuations in production costs or sales [8] - Tongling Nonferrous Metals has reported significant price increases in its main products, copper cathodes and gold, with low processing fees for copper concentrate [8] - New Yisheng has set the initial transfer price at 328 yuan per share, reflecting a 6.6% discount from the closing price [9] Group 7 - Lichong Group has signed a strategic cooperation agreement with Weijing Intelligent to extend its business into humanoid robotics [10] - Poly Development plans to transfer 4.512 billion shares to Poly Group, making it the controlling shareholder [10] - Huajian Group's executives plan to collectively reduce their holdings by 1.05 million shares [10][11]

Core Viewpoint - The company has received approval from the National Medical Products Administration for the clinical trial of SQ-129 vitreous sustained-release injection, a modified new drug aimed at treating diabetic macular edema and macular edema caused by retinal vein occlusion [1] Group 1: Product Development - SQ-129 vitreous sustained-release injection is classified as a chemical drug type 2.2 modified new drug [1] - The clinical application is intended for (1) treatment of diabetic macular edema (DME) in adult patients; (2) treatment of macular edema caused by branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO) in adult patients [1] - The company has completed various studies, including pharmaceutical and non-clinical pharmacology and toxicology, demonstrating good safety and clinical development value for SQ-129 [1] Group 2: Market Context - Currently, there are no approved products in the domestic and international markets for SQ-129 [1]

Core Viewpoint - The company has received approval from the National Medical Products Administration for the clinical trial of SQ-129 vitreous sustained-release injection, which is a modified new drug in category 2.2 aimed at treating diabetic macular edema and macular edema caused by retinal vein occlusion [1] Group 1: Product Development - SQ-129 vitreous sustained-release injection is developed for treating adult patients with diabetic macular edema (DME) [1] - The injection is also intended for adult patients suffering from macular edema due to branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO) [1] - The company has completed various studies, including pharmaceutical and non-clinical pharmacology and toxicology, demonstrating good safety and clinical development value for SQ-129 [1] Group 2: Market Context - Currently, there are no approved products in the domestic and international markets for SQ-129 vitreous sustained-release injection [1]

Core Viewpoint - The company has received approval from the National Medical Products Administration for the clinical trial of SQ-129 vitreous sustained-release injection, a new drug aimed at treating diabetic macular edema and macular edema caused by retinal vein occlusion [2]. Group 1: Product Development - SQ-129 vitreous sustained-release injection is classified as a Category 2.2 modified new chemical drug [2]. - The clinical indications for SQ-129 include treatment for adult patients with diabetic macular edema (DME) and macular edema due to branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO) [2]. - The company has completed various studies, including pharmaceutical and non-clinical pharmacology and toxicology, demonstrating good safety and clinical development value for SQ-129 [2]. Group 2: Market Context - Currently, there are no approved products in the domestic and international markets for SQ-129 [2]. - Following the approval of the clinical trial, the company must conduct clinical research according to the approval document and obtain further approval from the National Medical Products Administration before the product can be marketed [2].

Core Viewpoint - The company has received approval from the National Medical Products Administration for the clinical trial of SQ-129, a sustained-release injection for the treatment of diabetic macular edema and macular edema caused by retinal vein occlusion [1] Group 1 - The SQ-129 sustained-release injection is classified as a category 2 modified new chemical drug [1] - The clinical trial aims to treat adult patients with diabetic macular edema (DME) [1] - The clinical trial also targets adult patients with macular edema caused by branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO) [1]

Core Viewpoint - The company has received approval from the National Medical Products Administration for clinical trials of SQ-129, a vitreous body sustained-release injection aimed at treating diabetic macular edema (DME) and macular edema caused by branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO) [1] Summary by Categories Product Development - SQ-129 is classified as a Class 2 modified new chemical drug and has completed various studies including pharmaceutical and non-clinical pharmacology and toxicology, demonstrating good safety and clinical development value [1] - There are currently no approved products of this kind available in the domestic and international markets [1]