Core Viewpoint - The article discusses serious adverse events related to COVID-19 vaccines, particularly focusing on the Pfizer/BioNTech and Moderna trials, highlighting issues with trial protocols and regulatory oversight [1][2][3]. Group 1: Vaccine Trials and Regulatory Oversight - The Pfizer and Moderna vaccines received Emergency Use Authorization (EUA) after only 20 weeks of testing, which is atypical for vaccine trials [2]. - A forensic review of 38 deaths during the Pfizer vaccine trial revealed that regulators were not informed of two deaths, including one possibly linked to "sudden cardiac death," which could have influenced the approval process [3]. - The authors argue that had accurate data been presented to the FDA's Advisory Committee, it would have been evident that the vaccine did not save lives [3]. Group 2: Data Discrepancies and Health Risks - The article highlights a 3.7-fold increase in cardiac events among subjects receiving the BNT162b2 vaccine compared to the placebo, indicating significant data discrepancies [4]. - By the time the FDA and CDC acknowledged increased risks of myocarditis and pericarditis, many teenagers had already been vaccinated, with the risks downplayed to parents [5]. Group 3: Recommendations for Regulatory Reform - The authors conclude that restoring public trust in regulatory agencies requires significant policy changes, including the repeal of the PREP Act to prevent inadequately tested treatments from being administered [6].

Group 1 - The analyst has over 10 years of experience researching companies across various sectors, including commodities and technology [1] - The focus has shifted from writing a blog to creating a value investing-focused YouTube channel, where hundreds of companies have been researched [1] - The analyst expresses a particular interest in metals and mining stocks, while also being comfortable with consumer discretionary, staples, REITs, and utilities [1]

Group 1 - The analyst has over 10 years of experience researching more than 1000 companies across various sectors including commodities and technology [1] - The focus has shifted from writing a blog to creating a value investing-focused YouTube channel, where hundreds of companies have been researched [1] - The analyst expresses a particular interest in metals and mining stocks, while also being comfortable with other industries such as consumer discretionary, REITs, and utilities [1]

复星医药（600196）(600196.SH)发布公告，2025年12月9日，公司控股子公司药友制药、复星医药产业 与辉瑞共同签订《许可协议》，(其中主要包括)由药友制药就口服小分子胰高血糖素样肽-1受体(GLP- 1R)激动剂(包括YP05002)及含有该活性成分的产品授予辉瑞于许可区域(即全球范围)及领域(人类、动物 所有适应症的治疗、诊断及预防)独家开发、使用、生产及商业化权利;就本次许可，药友制药将有权依 约获得(其中包括)不可退还的首付款1.5亿美元及基于许可产品临床、商业化进展获得开发里程碑付款至 多3.5亿美元。此外，基于许可产品的年度净销售额达成情况，由辉瑞向药友制药依约支付至多15.85亿 美元的销售里程碑款项。 YP05002为集团自主研发并拥有自主知识产权的口服小分子胰高血糖素样肽-1受体(GLP-1R)激动剂;其主 要通过激活人的GLP-1R，促进胰腺的胰岛素分泌和降低胰高血糖素分泌，在胃肠道抑制胃排空和肠道 的蠕动,并通过影响中枢抑制食欲减少能量的摄入等机制，用于治疗2型糖尿病、肥胖症及其相关疾病。 YP05002拟用于代谢领域相关疾病的治疗，潜在适应症包括但不限于长期体重管理、2型 ...

创新药又现大单，复星医药收获1.5亿美元里程碑付款！ 12月9日晚间，复星医药公告称，公司控股子公司药友制药与辉瑞于2025年12月9日签订《许可协议》， 药友制药就口服小分子胰高血糖素样肽-1受体（GLP-1R）激动剂（包括YP05002）及含有该活性成分的 产品授予辉瑞于全球范围及领域独家开发、使用、生产及商业化权利。 在公告中，复星医药明确表示药友制药将有权获得不可退还的首付款1.5亿美元及至多3.5亿美元的开发 里程碑款项。此外，基于许可产品的年度净销售额达成情况，辉瑞将向药友制药支付至多15.85亿美元 的销售里程碑款项。该协议自2025年12月9日起生效。 值得注意的是，目前药友制药的小分子胰高血糖素样肽-1受体（GLP-1R）激动剂尚处于I期临床试验阶 段。无论最终该产品研发结果如何，复星医药都至少收获1.5亿美元(约合人民币10.6亿元)。至于此次重 磅押注，出钱的是国际医药巨头辉瑞。 公告显示，YP05002 为口服小分子胰高血糖素样肽-1受体（GLP-1R)激动剂；其主要通过激活人的GLP- 1R，促进胰腺的胰岛素分泌和降低胰高血糖素分泌，在胃肠道抑制胃排空和肠道的蠕动，并通过影响 中枢抑 ...

Pfizer has entered into an exclusive global collaboration and licensing deal with a unit of Shanghai Fosun Pharmaceutical for an early-stage weight-loss drug https://t.co/7etdqabjPx ...

来源：新浪财经-鹰眼工作室 上海复星医药（集团）股份有限公司（证券代码：600196，下称"复星医药"）12月9日公告称，公司控 股子公司重庆药友制药有限责任公司（下称"药友制药"）与全球生物制药巨头辉瑞公司（Pfizer Inc.） 签订《许可协议》。根据协议，药友制药将其自主研发的口服小分子胰高血糖素样肽-1受体（GLP- 1R）激动剂（包括YP05002）及相关产品的全球独家开发、使用、生产及商业化权利授予辉瑞，交易涉 及首付款1.5亿美元及潜在里程碑付款等多重收益。 协议核心内容：全球独家授权 GLP-1类药物成焦点 公告显示，本次协议为独家开发、使用、生产及商业化许可。药友制药授予辉瑞在全球范围内（人类及 动物所有适应症的治疗、诊断及预防领域）对YP05002及含该活性成分产品的独家权利。作为回报，药 友制药将获得不可退还的首付款1.5亿美元，以及基于临床开发和商业化进展的开发里程碑付款（最高 3.5亿美元）、基于销售达成的销售里程碑付款（最高15.85亿美元），并有权收取按年度净销售额至多 两位数百分比计算的特许权使用费。 作为全球领先的生物制药公司，辉瑞成立于1942年，总部位于美国特拉华州，在 ...

北京商报讯（记者 王寅浩 宋雨盈）12月9日，复星医药发布公告称，公司控股子公司药友制药就口服小 分子胰高血糖素样肽-1受体（GLP-1R）激动剂（包括YP05002）及含有该活性成分的产品授予辉瑞于全 球范围及领域（即人类、动物所有适应症的治疗、诊断及预防）独家开发、使用、生产及商业化权利。 就本次许可，药友制药将有权依约获得（其中包括）不可退还的首付款 1.5亿美元及基于许可产品临 床、商业化进展获得开发里程碑付款至多3.5亿美元。此外，基于许可产品的年度净销售额达成情况， 由辉瑞向药友制药依约支付至多15.85亿美元的销售里程碑款项。 ...

Core Insights - Fosun Pharma's subsidiary Yao Pharma has entered into an exclusive collaboration and license agreement with Pfizer for the development and commercialization of oral small-molecule GLP-1R agonists, including YP05002 [1][2] - Yao Pharma will receive an upfront payment of $150 million and potential milestone payments up to $1.935 billion, along with tiered royalties on sales if approved [1] - The partnership is seen as a significant milestone in Fosun Pharma's strategy of innovation and internationalization, aiming to address unmet clinical needs in metabolic diseases [3] Company Overview - Yao Pharma has developed small-molecule GLP-1R agonists with proprietary intellectual property rights, targeting metabolic diseases such as chronic weight management, type 2 diabetes, and non-alcoholic steatohepatitis (NASH) [2] - YP05002 is currently in Phase 1 clinical development in Australia, indicating progress in the drug's development pipeline [2] Strategic Implications - The collaboration with Pfizer is viewed as a recognition of Yao Pharma's R&D capabilities and aims to leverage Pfizer's global development experience to expedite the commercialization of YP05002 [3] - Fosun Pharma's leadership emphasizes the importance of collaboration in maximizing the value of innovation and addressing global health challenges related to obesity and metabolic diseases [3]

Core Viewpoint - Fosun Pharma announced a licensing agreement with Pfizer for the exclusive global development, use, production, and commercialization rights of GLP-1R agonists, including YP05002, for all human and animal indications [1] Group 1: Agreement Details - The agreement involves Fosun Pharma's subsidiary, Chongqing Yaoyou Pharmaceutical Co., Ltd., and Shanghai Fosun Pharmaceutical Industry Development Co., Ltd. [1] - Yaoyou Pharmaceutical will complete Phase I clinical trials of YP05002 in Australia and grant Pfizer exclusive rights for further global development and commercialization [1] Group 2: Financial Aspects - Yaoyou Pharmaceutical will receive an upfront payment of $150 million [1] - The company is eligible for milestone payments up to $1.935 billion related to specific development, registration, and commercial milestones, along with tiered royalties after product approval [1]