近年来，步长制药（603858）在创新药研发、资本市场回报及公益事业领域受到市场关注。从多领域创 新药管线的加速推进，到持续加码的分红回购计划，再到十八年深耕公益的坚守，步长制药以全方位布 局展现着医药头部企业的战略纵深。 自成立以来，步长制药始终以清晰战略引领发展航向，秉持"中国的强生、世界的步长"愿景，践行"以 中药为基础，向生物药、疫苗等医药高科技行业扩张"的核心战略，坚守"聚焦大行业、培育大品种"的 发展路径，逐步实现从单一中药企业向综合性医药集团的跨越。 在核心中成药领域，步长制药已构建起差异化竞争优势。公司以"脑心同治论"为理论根基，研发培育出 脑心通胶囊、稳心颗粒、丹红注射液三大独家专利品种，形成覆盖中风、心律失常、供血不足、缺血梗 塞等常见心脑血管疾病的完整治疗体系，精准契合"大病、慢病"领域的临床需求。目前，公司具备胶囊 剂、颗粒剂、针剂等多种剂型生产能力，上市产品广泛覆盖中成药传统优势领域，构建起"立足心脑血 管市场、聚焦大病种、培育大品种"的立体产品格局。 多元化布局成为公司拓展成长边界的关键。除核心产品外，步长制药已开发储备宣肺败毒颗粒、银杏蜜 环口服溶液、参芎葡萄糖注射液等多款潜力产 ...

Core Viewpoint - Recently, Buchang Pharma (603858.SH) has gained market attention for its dual strength in high-quality development and social responsibility, showcasing its commitment through innovative drug development, capital market returns, and public welfare initiatives [1] Group 1: Innovative Drug Pipeline - Buchang Pharma has accelerated its efforts in innovative drug development, establishing a diversified pipeline that includes patented traditional Chinese medicine, biopharmaceuticals, chemical drugs, and vaccines, with significant breakthroughs expected by 2025 [2] - The company is advancing its first Class 1 new drug, Epoetin α, aimed at treating renal anemia and chemotherapy-induced anemia, which could fill a gap in the domestic long-acting EPO market valued at 15 billion [2] - The first biosimilar drug, Adalimumab injection, is under review, targeting multiple autoimmune diseases with substantial market potential [2] - The company is also progressing in clinical trials for several targeted cancer therapies, including BC001 and BC008-1A [2] Group 2: Traditional Chinese Medicine and Chemical Drug Expansion - In traditional Chinese medicine, the company is advancing clinical trials for Qi-tonifying granules and heart failure treatments, reinforcing its core advantages [4] - In the chemical drug sector, Buchang Pharma has launched 17 new generic drugs in 2023, including products that tap into a 20 billion antiviral drug market [4] - By the end of 2025, the company expects 39 products to have passed evaluations, with several winning bids in centralized procurement to expand market share [4] Group 3: Globalization Strategy - Buchang Pharma is actively pursuing a globalization strategy, with its products now available in 38 countries and regions across Asia, Europe, Africa, and the Americas [5] - The company has signed exclusive supply agreements for its new drug Epoetin α in Southeast Asia and is collaborating with Russian firms to promote its products in the Eurasian Economic Union [5] - Several traditional Chinese medicine products have received international recognition and registration, enhancing the company's global footprint [7] Group 4: Shareholder Returns - The company has maintained a stable return mechanism for investors, with cumulative dividends reaching 7.948 billion and share buybacks totaling 1.744 billion since its listing [8] - In 2025, the company repurchased 6.6206 million shares, demonstrating confidence in its future growth [8] Group 5: Corporate Social Responsibility - Buchang Pharma has been committed to social responsibility, sponsoring the "Together, Build China's Heart" public welfare project for 18 years, providing medical assistance across multiple specialties [9] - The company has contributed nearly 33 billion in taxes, supporting regional economic development [11] - The chairman emphasized the company's focus on innovation, global expansion, and social responsibility as key drivers for future growth [11]

Core Viewpoint - Shandong Buchang Pharmaceutical's subsidiary, Luzhou Buchang, has signed an exclusive supply agreement with Malaysian company MEDISPEC, marking a significant step in the company's "Traditional Chinese Medicine Internationalization" strategy [1] Group 1: Internationalization Strategy - The signing of the agreement reflects the deepening of Buchang Pharmaceutical's internationalization strategy, with recent product registrations in Malaysia, Mongolia, and Indonesia [2] - The company's sales network now covers dozens of countries, including the US, Canada, and Vietnam, and is actively expanding into Latin America [2] - Buchang Pharmaceutical aims to make "Chinese prescriptions" an international medical option and promote traditional Chinese culture [2] Group 2: R&D and Product Development - Buchang Pharmaceutical is advancing in innovative drug development, with significant progress in its pipeline across biological, traditional Chinese, and chemical drugs [4] - The company has received approvals for 17 generic drugs in 2023, with over 170 products included in the 2025 National Medical Insurance Directory, including 73 exclusive products [4] - Exclusive products have generated over 10.3 billion yuan in sales in the first three quarters of 2025, providing strong support for ongoing innovation [4] Group 3: Shareholder Returns - The company has returned 7.948 billion yuan to shareholders through regular high dividends and share buybacks, exceeding the total IPO fundraising amount [5] - In 2025 alone, the company repurchased 6.6206 million shares, spending nearly 100 million yuan, and completed the cancellation of 51.47 million shares [5] Group 4: Social Responsibility - Buchang Pharmaceutical has sponsored the "Together, Build China's Heart" public welfare project for 18 consecutive years, providing medical assistance to over a million people [6] - The company emphasizes the dual focus on innovation and social responsibility, aiming to create greater social value while advancing pharmaceutical innovation [6]

Core Viewpoint - Recently, Buchang Pharma has gained market attention for its innovation in drug development, capital market returns, and commitment to public welfare, showcasing the company's responsibility and dedication in the pharmaceutical industry [1] Innovation Drug Pipeline - Buchang Pharma has made significant advancements in its innovation drug pipeline, covering three major areas: biopharmaceuticals, traditional Chinese medicine, and chemical drugs [2] - The company is accelerating the application of its first Class 1 new drug, Epoetin Alfa, targeting renal anemia and chemotherapy-induced anemia, which could fill a gap in the domestic long-acting EPO market valued at 15 billion [2] - The first biosimilar drug, Adalimumab injection, is under review, targeting multiple autoimmune diseases with substantial market potential [2] - The company is advancing its Class 1 biopharmaceutical BC001 for late-stage gastric cancer and has several targeted cancer drugs in critical clinical development stages [2][4] Traditional Chinese Medicine and Chemical Drug Expansion - In traditional Chinese medicine, the company has completed Phase II clinical trials for its Qi-tonifying granules and is set to start Phase II/III trials for its heart failure treatment granules in May 2025 [4] - In the chemical drug sector, Buchang Pharma has launched 17 new generic drugs in 2023, including products that target a 20 billion market for antiviral drugs and expand its muscle relaxant market [4] - The company has successfully renewed contracts for exclusive products in the 2025 National Medical Insurance Directory, with total sales exceeding 10.3 billion in the first three quarters [4] Shareholder Returns - Buchang Pharma has established a stable return mechanism for investors, with cumulative dividends reaching 7.948 billion and share buybacks totaling 1.744 billion since its listing [5] - In 2025, the company has repurchased 6.6206 million shares, with a total repurchase amount nearing 100 million, demonstrating confidence in its future development [5] Corporate Social Responsibility - Since its inception, Buchang Pharma has adhered to its mission of "creating health for humanity," actively engaging in social responsibility through the "Together, Build China's Heart" initiative for 18 years [6] - The initiative has expanded from congenital heart disease to various medical fields, providing comprehensive medical assistance to over 1 million patients [6] - The company has contributed nearly 33 billion in taxes nationwide, supporting regional economic development [6] Future Outlook - The chairman of Buchang Pharma, Zhao Tao, emphasized the company's commitment to innovation-driven development and social responsibility, aiming to lead industry growth and create greater social value [7]

Core Viewpoint - The company is accelerating its internationalization and innovation efforts, with over 170 products included in the 2025 National Medical Insurance Directory, and is focusing on expanding its global market presence through strategic partnerships and product registrations [1][3][4]. Group 1: Product Development and Innovation - The company has 73 exclusive products in the 2025 National Medical Insurance Directory, including 63 traditional Chinese medicines, 9 chemical drugs, and 1 vaccine [1]. - The company is advancing its first-class new drug, Efparepoetin alfa, which has a cumulative R&D investment of approximately 51.24 million RMB as of September 30, 2025, and is expected to have significant market potential as it is the first of its kind in China [3]. - The company has successfully registered multiple products in various countries, including Malaysia, Canada, and Mongolia, indicating a strong international market strategy [5][6]. Group 2: Policy Support and Market Expansion - A recent guideline issued by five government departments aims to enhance the overseas service ecosystem for Chinese enterprises, which will support the company's international expansion efforts [4]. - The company has expanded its product sales to numerous countries and regions, including the United States, Canada, and several countries in Asia, Europe, and Africa, with ongoing registration efforts in Australia, Brazil, and the UAE [5]. Group 3: Corporate Social Responsibility - The company has contributed nearly 33 billion RMB in taxes, supporting local economic development and demonstrating its commitment to social responsibility [7]. - The "Together, Build a Chinese Heart" project has been ongoing for 18 years, providing medical assistance to Tibetan and minority communities, showcasing the company's dedication to social welfare [8][10]. - The company emphasizes long-term commitment to public welfare, aiming to set an industry example in corporate citizenship [7][10].

Core Viewpoint - Recently, two major products from Buchang Pharma, Xuanfei Baidu Granules and Tongbianling Capsules, successfully passed the Indonesian Ministry of Health's review and obtained drug registration certificates [1] Group 1: Product Registration - Xuanfei Baidu Granules has previously been registered in Canada, Uzbekistan, and Kazakhstan [1] - Along with the new products, eight renewal registration products, including Buchang Stabilizing Granules, Kelu Oral Liquid, and Yangzheng Heji, were also successfully approved [1] Group 2: Market Expansion - Currently, Buchang Pharma has over 20 products listed for sale in Indonesia [1] - The addition of these new products not only enriches Buchang Pharma's product matrix in Indonesia but also represents a solid step in the "internationalization of traditional Chinese medicine" strategy [1] - This move highlights the unique value and broad recognition of traditional Chinese medicine on the international stage [1]

Group 1 - The company successfully renewed the inclusion of its products, Xuanfei Baidu Granules and Danhong Injection, in the National Medical Insurance Catalog for 2025 [1][3] - Xuanfei Baidu Granules are indicated for clearing heat and detoxifying, used for epidemic diseases caused by damp-heat obstructing the lungs, with symptoms including fever, cough, and shortness of breath [1][2] - Danhong Injection is indicated for activating blood circulation and relieving obstruction, used for chest pain and stroke caused by blood stasis, with symptoms including chest pain, palpitations, and limb numbness [2] Group 2 - The National Medical Insurance Catalog will officially take effect on January 1, 2026, with specific execution requirements to be determined by government departments [3] - The sales performance of the drugs may be influenced by multiple factors, including changes in the market environment, leading to uncertainty [3]

Core Viewpoint - Shandong Buchang Pharmaceutical Co., Ltd. successfully renewed the inclusion of its products Xuanfei Baidu Granules and Danhong Injection in the National Medical Insurance Directory for 2025, which is expected to positively impact the company's market position and sales performance [1][3]. Product Information - Xuanfei Baidu Granules are indicated for clearing lung heat and detoxifying, used for damp-heat obstructing the lungs, with symptoms including fever, cough, and shortness of breath [1]. - Danhong Injection is used for promoting blood circulation and alleviating pain, indicated for conditions such as chest pain and stroke, with symptoms including chest tightness and limb numbness [2]. Sales Impact - The National Medical Insurance Directory will be officially implemented on January 1, 2026, and the sales performance of the drugs may be influenced by various market factors, indicating a level of uncertainty [3].

Core Viewpoint - The company, Buchang Pharma, successfully retained its drugs Xuanfei Baidu Granules and Danhong Injection in the National Medical Insurance Directory for 2025, ensuring continued access to these products under national health insurance programs [1] Group 1: Drug Information - Xuanfei Baidu Granules are indicated for clearing heat and detoxifying the lungs, used for epidemic diseases caused by damp-heat obstructing the lungs, with symptoms including fever, cough, and shortness of breath [1] - Danhong Injection is used for promoting blood circulation and alleviating blood stasis, indicated for conditions such as chest pain and stroke, with symptoms including chest tightness and limb numbness [1]

Group 1: Epidemic Overview - The recent outbreak of Chikungunya fever in southern China has led to nearly 3,000 new cases reported in just one week, primarily in Guangdong province, affecting over ten cities [1][3] - The majority of cases are concentrated in Foshan, accounting for 95% of the total cases in Guangdong, with no severe cases or deaths reported so far [3] Group 2: Government Response and Guidelines - The National Health Commission has released the "Chikungunya Fever Diagnosis and Treatment Plan (2025 Edition)," emphasizing that the disease is preventable, controllable, and treatable [3][6] - The plan incorporates traditional Chinese medicine (TCM) approaches, highlighting the role of TCM in alleviating symptoms and promoting recovery [6] Group 3: Company Initiatives in Diagnostics and Treatment - Several listed companies in the IVD (in vitro diagnostics) sector are actively developing testing products and treatment solutions for Chikungunya fever [4][5] - Shenzhen BGI Technology Co., Ltd. has introduced the T1+ gene sequencer, which can provide comprehensive genomic analysis within 6-8 hours, aiding in rapid response to the outbreak [4] - Wanfu Biology has developed multiple Chikungunya virus detection products, creating a closed-loop system for monitoring and diagnosis [4] Group 4: Traditional Chinese Medicine Applications - TCM is being utilized for symptomatic treatment of Chikungunya fever, with specific formulations recommended for managing symptoms like fever and joint pain [6][7] - Companies such as Guangdong Yifang Pharmaceutical and Step Long Pharmaceutical are producing traditional Chinese medicines that may assist in treating Chikungunya fever [7]