格隆汇1月29日丨上海医药(601607.SH)公布，公司下属正大青春宝药业有限公司（简称"青春宝"）研发 的"七味防己黄芪颗粒"（简称"该项目"）收到国家药品监督管理局核准签发的《药物临床试验批准通知 书》，七味防己黄芪颗粒处方由天津中医药大学结合中医经典理论和临床实践，在"防己黄芪汤"基础上 进行配伍化裁而来。该项目由青春宝与天津中医药大学等单位合作研发，并拥有核心知识产权。截至本 公告披露日，该项目已累计投入研发费用约1,380万元人民币。 ...

上海医药集团股份有限公司 关于芪苓颗粒获得临床试验批准通知书的公告 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，上海医药集团股份有限公司（以下简称"上海医药"或"公司"）下 属正大青春宝药业有限公司（以下简称"青春宝"）自主研发的"芪苓颗粒"（以 下简称"该项目"）收到国家药品监督管理局（以下简称"国家药监局"）核准 签发的《药物临床试验批准通知书》，现将有关情况公告如下： 一、该项目基本信息 药物名称：芪苓颗粒 剂型：颗粒剂 申请事项：境内生产药品注册临床试验 证券代码：601607 证券简称：上海医药 编号：临2026-009 1 受理号：CXZL2500071 通知书编号：2025LP03031 审批结论：根据《中华人民共和国药品管理法》及有关规定，经审查，2025 年 9 月 1 日受理的芪苓颗粒临床试验申请符合药品注册的有关要求，在进一步完 善临床试验方案的基础上，同意开展用于痛风发作间歇期湿浊瘀阻证的临床试验。 二、该项目研发及注册情况 芪苓颗粒处方源自杭州市中医院的临床验方。人用经验研究表明本品可 ...

证券代码：601607 证券简称：上海医药 编号：临2026-008 申请事项：境内生产药品注册临床试验 受理号：CXZL2500097 通知书编号：2025LP03576 上海医药集团股份有限公司 关于七味防己黄芪颗粒获得临床试验批准通知书的公告 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，上海医药集团股份有限公司（以下简称"上海医药"或"公司"）下 属正大青春宝药业有限公司（以下简称"青春宝"）研发的"七味防己黄芪颗粒" （以下简称"该项目"）收到国家药品监督管理局（以下简称"国家药监局"）核 准签发的《药物临床试验批准通知书》，现将有关情况公告如下： 一、该项目基本信息 药物名称：七味防己黄芪颗粒 剂型：颗粒剂 二、该项目研发及注册情况 七味防己黄芪颗粒处方由天津中医药大学结合中医经典理论和临床实践，在 "防己黄芪汤"基础上进行配伍化裁而来。该项目由青春宝与天津中医药大学等 单位合作研发，并拥有核心知识产权。截至本公告披露日，该项目已累计投入研 发费用约 1,380 万元人民币。 1 三、同类药物市场情况 ...

上海医药公告，下属正大青春宝药业有限公司研发的"七味防己黄芪颗粒"收到国家药品监督管理局核准 签发的《药物临床试验批准通知书》。该药物为颗粒剂型，用于慢性心力衰竭的临床试验。项目由青春 宝与天津中医药大学等合作研发，累计投入研发费用约1380万元人民币。该产品尚未在国内外上市。 ...

上海医药公告，下属正大青春宝药业有限公司自主研发的"芪苓颗粒"收到国家药品监督管理局核准签发 的《药物临床试验批准通知书》。芪苓颗粒为颗粒剂，用于痛风发作间歇期湿浊瘀阻证的临床试验。芪 苓颗粒处方源自杭州市中医院的临床验方，由青春宝自主研发，拥有核心知识产权。截至本公告披露 日，该项目已累计投入研发费用约1142万元人民币。 ...

Core Viewpoint - Shanghai Pharmaceuticals (601607.SH) has received a drug registration certificate from the Health Sciences Authority (HSA) of Singapore for its Pregabalin capsules, allowing the product to be marketed [1] Group 1: Product Approval and Indications - Pregabalin capsules are primarily used for the treatment of postherpetic neuralgia, diabetic peripheral neuropathy, fibromyalgia, spinal cord injury-related neuropathic pain, and as an adjunctive treatment for epilepsy [1] - The product's research and development were completed by Changzhou Pharmaceutical Factory in October 2019, and it received approval from the U.S. Food and Drug Administration in July 2021 [1] Group 2: Market Expansion and Investment - The drug has also been approved for market entry in Thailand by June 2025, indicating a strategic expansion into Southeast Asian markets [1] - The company has invested approximately RMB 2.19 million in research and development for the product's launch in Southeast Asia, which includes Thailand, Singapore, Malaysia, and the Philippines [1]

Group 1 - Shanghai Pharmaceuticals has received approval for the production of Avatrombopag Maleate Tablets from the National Medical Products Administration [1][2] - The drug is indicated for adult patients with chronic liver disease-related thrombocytopenia undergoing elective diagnostic procedures or surgery, and for adults with chronic primary immune thrombocytopenia (ITP) who have had inadequate responses to previous treatments [3] - The company has invested approximately RMB 9.8961 million in the research and development of this drug as of the announcement date [3] Group 2 - The drug's approval is expected to enhance market share and competitiveness, benefiting from greater support in medical insurance and procurement due to its new registration classification [5] - The total procurement amount for Avatrombopag Maleate Tablets in hospitals in mainland China is projected to be RMB 566.56 million in 2024 [4] Group 3 - Shanghai Pharmaceuticals' subsidiary, Changzhou Pharmaceutical Factory, has received a drug registration certificate for Pregabalin Capsules from the Health Sciences Authority of Singapore, allowing it to market the drug in Singapore [8][9] - Pregabalin Capsules are indicated for the treatment of neuropathic pain and as an adjunct therapy for epilepsy, with a total investment of approximately RMB 2.19 million in R&D for the Southeast Asian market [9] - The sales revenue for Pregabalin Capsules in Singapore is estimated to be USD 2 million in 2024 [11]

Core Viewpoint - Shanghai Pharmaceuticals announced that its subsidiary, Changzhou Pharmaceutical Factory, received a drug registration certificate from the Health Sciences Authority (HSA) of Singapore for the drug Pregabalin capsules, which has been approved for market launch [1]. Group 1 - The drug Pregabalin capsules have been officially approved for sale in Singapore [1]. - The approval was granted by the Health Sciences Authority (HSA) of Singapore [1].

Core Viewpoint - Shanghai Pharmaceuticals has received approval from the Singapore Food and Drug Administration for the marketing of Pregabalin capsules, indicating a significant milestone for the company in expanding its product offerings in the international market [1]. Group 1 - The approved Pregabalin capsules are primarily used for treating postherpetic neuralgia, diabetic peripheral neuropathy, fibromyalgia, and neuropathic pain due to spinal cord injury, as well as for adjunctive treatment of epilepsy [1].

Core Viewpoint - Shanghai Pharmaceuticals (02607.HK) announced that its subsidiary, Changzhou Pharmaceutical Factory, has received a drug registration certificate from the Health Sciences Authority (HSA) of Singapore for Pregabalin capsules, which have been approved for market launch [1] Group 1 - The approved drug, Pregabalin capsules, is primarily used for the treatment of postherpetic neuralgia, diabetic peripheral neuropathy, fibromyalgia, and neuropathic pain due to spinal cord injury, as well as for adjunctive treatment of epilepsy [1]