一．药品基本信息 药品名称：KHN707片 登录新浪财经APP 搜索【信披】查看更多考评等级 证券代码：002773 证券简称：康弘药业 公告编号：2026-005 成都康弘药业集团股份有限公司 关于公司收到药物临床试验批准通知书的公告 本公司及董事会全体成员保证信息披露内容的真实、准确和完整，没有虚假记载、误导性陈述或重大遗 漏。 近日，成都康弘药业集团股份有限公司（以下简称"公司"）收到国家药品监督管理局签发的《药物临床 试验批准通知书》。现将相关情况公告如下： 二．产品简介 KHN707片是我公司自主研发的选择性食欲素2（OX2R）受体拮抗剂，属于化药1类创新药，剂型为片 剂。前期已完成的研究结果显示KHN707片安全性较好，且在失眠模型中具有良好的治疗作用，预期临 床应用前景较好。 三．对公司的影响 由于药品从研发、临床试验、审评和审批的结果以及时间都具有一定的不确定性，敬请广大投资者谨慎 决策，注意投资风险。 特此公告。 剂型：片剂 适应症：失眠症 注册分类：化学药品1类 受理号：CXHL2501386、CXHL2501387 审批结论：同意开展用于失眠症的临床试验 成都康弘药业集团股份有限公司 董 ...

Core Insights - Jiangsu Kangyuan Pharmaceutical Co., Ltd. reported a revenue of 1.642 billion yuan and a net profit of 142 million yuan for the first half of 2025, despite facing complex external environments and fluctuations in drug demand [1] Group 1: Traditional Chinese Medicine Innovation - The core business segment of Kangyuan Pharmaceutical, traditional Chinese medicine (TCM) research, achieved dual breakthroughs in approvals and clinical progress, with 214 drug production licenses obtained, including 50 exclusive varieties [2] - Notable TCM innovations include the approval of Yunu Jian granules for digestive system diseases and clinical trial approvals for Lian Shen Menopausal granules and Gu Ben Xiao Zhen granules, expanding the company's offerings in gynecology and dermatology [2] - Several TCM drugs are in critical clinical stages, with Su Xin Tong Qiao granules and Shuang Yu granules entering the Pre-NDA stage, targeting allergic rhinitis and influenza, respectively [2] Group 2: Chemical and Biological Drugs - In the chemical and biological drug sectors, Kangyuan Pharmaceutical made significant progress in innovative drugs targeting major diseases, focusing on unmet clinical needs in cardiovascular, neurological, metabolic, and autoimmune areas [4] - The Alzheimer's treatment drug Fluoropropylamine tablets has completed Phase II clinical data collection and is expected to start Phase III trials in 2025 [4] - The company is also advancing several other drugs in clinical stages, including those for benign prostatic hyperplasia and acute ischemic stroke [4] Group 3: International Expansion and Technological Empowerment - Kangyuan Pharmaceutical achieved breakthroughs in overseas business, obtaining two natural health product licenses in Canada and two proprietary Chinese medicine licenses in Hong Kong, enhancing the internationalization of TCM [6] - The company is committed to accelerating TCM registration in multiple countries, positioning overseas markets as potential growth points [6] - The establishment of research platforms, including a national key laboratory for TCM manufacturing process control, has led to the approval of five national projects and the filing of 80 invention patents during the reporting period [7]

Summary of Key Points Core Viewpoint - Guangxi Wuzhou Zhongheng Group Co., Ltd. has acquired a patent for a drug technology aimed at treating chronic heart failure through its wholly-owned subsidiary, Zhongheng Innovation, for a total price of RMB 55 million [1][2][3]. Transaction Overview - The acquisition involves a drug technology (patent) for treating chronic heart failure, with the transaction price set at RMB 55 million, excluding tax [1][3]. - The transaction has been approved by the company's board of directors and does not require shareholder approval [1][3]. - The contract was signed on August 1, 2025, following the receipt of qualification confirmation from the Shanghai Technology Exchange [2][3]. Transaction Details - The project was publicly listed for transfer on May 20, 2025, with a minimum bid price of RMB 55 million and a deposit of RMB 500,000 [3]. - Payment for the transfer will be made in stages, with an initial payment of at least RMB 5 million due within 10 working days after the contract takes effect [3][6]. Drug Technology Information - The drug, referred to as LZ-01, is a novel compound discovered by the Navy Medical University of the People's Liberation Army, which significantly improves myocardial energy metabolism and heart function in chronic heart failure patients [5][6]. - The drug is classified as a Class 1 innovative chemical drug, administered orally, and is currently in the preclinical research phase [6]. Impact on the Company - This acquisition aligns with the company's strategic focus on unmet clinical needs and potential markets, particularly in cardiovascular and metabolic diseases [8]. - The transaction is expected to enhance the company's product line and market competitiveness without significantly impacting its short-term financial performance [8].