来源：格隆汇APP 格隆汇8月1日｜美国总统特朗普周四致函欧洲制药公司，要求其将美国消费者的药品价格降至其他发达 国家的最低水平，导致欧洲制药公司股价早盘下跌。葛兰素史克、阿斯利康、诺和诺德和赛诺菲的股价 分别下跌1.7%、2.8%、4.2%和1.2%，诺和诺德股价跌至四年低点。斯托克欧洲600医疗保健指数下跌 1.8%。 ...

特朗普要求降低药品价格后，欧洲制药股下跌 金十数据8月1日讯，美国总统特朗普周四致函欧洲制药公司，要求其将美国消费者的药品价格降至其他 发达国家的最低水平，导致欧洲制药公司股价早盘下跌。葛兰素史克、阿斯利康、诺和诺德和赛诺菲的 股价分别下跌1.7%、2.8%、4.2%和1.2%，诺和诺德股价跌至四年低点。斯托克欧洲600医疗保健指数下 跌1.8%。 ...

格隆汇8月1日｜阿斯利康欧股股价下跌3%，此前特朗普要求制药公司降低药品价格。 ...

特朗普要求制药巨头降低美国药价 诺和诺德跌超6% 智通财经8月1日电，诺和诺德跌超6%，阿斯利康跌超3%。美国总统特朗普周四表示，他已要求全球主 要制药公司在未来60天内采取措施降低美国药品价格。 ...

人民财讯8月1日电，阿斯利康8月1日宣布，伟立瑞（英文商品名：Ultomiris，通用名：瑞利珠单抗注射 液）在中国正式获批用于治疗抗水通道蛋白4（AQP4）抗体阳性的成人视神经脊髓炎谱系疾病 （NMOSD）患者。 （原标题：阿斯利康：伟立瑞®在华获批用于治疗视神经脊髓炎谱系疾病成人患者） ...

人民财讯8月1日电，阿斯利康8月1日宣布，伟立瑞(英文商品名：Ultomiris，通用名：瑞利珠单抗注射 液)在中国正式获批用于治疗抗水通道蛋白4(AQP4)抗体阳性的成人视神经脊髓炎谱系疾病(NMOSD)患 者。 ...

Group 1 - President Trump has sent letters to 17 major pharmaceutical companies, demanding specific actions to lower drug prices in the U.S. within 60 days, or he will use "all available means" to protect American families from "price gouging" [1][2] - The companies that received the letters include Pfizer, Novo Nordisk, Johnson & Johnson, and others, with a focus on commitments such as providing "most favored nation" pricing for Medicaid patients and direct sales to consumers [1][2] - Trump highlighted that U.S. drug prices are significantly higher than those in other developed countries, with average prescription drug prices being 2 to 3 times higher, and some drugs up to 10 times more expensive [2] Group 2 - Following the announcement, stock prices of several pharmaceutical companies dropped, with Sanofi falling over 8%, and others like Bristol-Myers Squibb and Novo Nordisk declining nearly 5% [2] - The Pharmaceutical Research and Manufacturers of America criticized the introduction of "foreign price controls," arguing it would undermine U.S. innovation and harm patients and workers [3] - Companies like Pfizer and Novartis stated they are working on solutions to make medications more affordable for American patients, with AstraZeneca considering price reductions and direct sales models [3]

Core Viewpoint - AstraZeneca and Merck have announced that the National Medical Products Administration (NMPA) has approved the use of the PARP inhibitor Olaparib in combination with Abiraterone and Prednisone or Prednisolone for the treatment of adult patients with metastatic castration-resistant prostate cancer carrying germline or somatic BRCA mutations [1] Group 1: Approval and Clinical Data - The NMPA's approval is based on the results of the PROpel Phase III trial, which included global and Chinese cohort subgroup analyses [1] - Data from the global cohort of patients with BRCA mutations showed a significant improvement in imaging progression-free survival with the combination of Olaparib and Abiraterone compared to Abiraterone monotherapy [1] - Although the sample size of the Chinese cohort was small and interpretation was limited, the study data also indicated improvements consistent with global cohort trends, with no new safety issues identified [1] Group 2: Expert Commentary - Professor Ye Dingwei, a leading researcher of the PROpel study in China, emphasized that patients with BRCA mutation metastatic castration-resistant prostate cancer have poor prognoses and unmet clinical needs [1] - He stated that the PROpel study results allow for earlier use of Olaparib in treatment, improving patient outcomes and highlighting the potential of this innovative therapy to become a new treatment standard [1] Group 3: Company Strategy - Dr. He Jing, AstraZeneca's Global Senior Vice President and Head of Global R&D in China, expressed excitement over the PROpel study results and indicated that the company will continue to leverage both in-house research and external collaborations to enrich its pipeline for the benefit of more cancer patients [1]

Core Viewpoint - Merck has received approval from the National Medical Products Administration of China for its PARP inhibitor, Olaparib, in combination with Abiraterone and Prednisone or Prednisolone for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) carrying germline or somatic BRCA mutations (gBRCAm or sBRCAm) [1] Group 1 - The approval of this combination therapy will provide advanced treatment options for more prostate cancer patients [1]

Group 1 - Merck announced that the National Medical Products Administration of China has officially approved its PARP inhibitor, Lapatinib (Olaparib), in combination with Abiraterone and Prednisone or Prednisolone for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) carrying germline or somatic BRCA mutations (gBRCAm or sBRCAm) [1]