四价流感疫苗普遍跌破百元，三价疫苗的降价更为极端，公费三价流感疫苗已创下6元/支历史新低中标 价。 近日，浙江省政府采购中心发布的浙江省疾控中心2025年群体性预防接种流感疫苗中标(成交)结果公告 显示，上海生物制品研究所有限责任公司(上海所)、长春生物制品研究所有限责任公司(长春所)、北京 科兴生物制品有限公司(北京科兴)三家公司中标，成交总价分别为780万、480万、440万，单价分别为6 元/支、6元/支、8.8元/支。 6月13日，赛诺菲对中新健康表示，"在2025—2026年流感季流感疫苗生产过程中，我们优化了免疫原性 和产品稳定性评估，于2024年12月完成了原液试生产，并进行了持续的研究和测试，所有结果均证明效 价稳定。" 据公开数据，2024年上半年，三价流感疫苗的批签发中，赛诺菲占比18%；四价流感疫苗的批签发中， 赛诺菲占比15%。在赛诺菲暂停供应期间，多家流感疫苗厂商相继宣布对流感疫苗进行降价，抢占市场 份额。 2024年5月，国药集团旗下长春所、武汉所、上海所的四价流感疫苗开始降价。中标价格由128元/支跌 破百元至88元/支，随后主流疫苗厂商华兰疫苗、北京科兴、金迪克等也紧步跟降。同 ...

2024年8月份，赛诺菲之所以暂停了2024-2025年流感季的三价流感疫苗以及四价流感疫苗销售，原因是 公司在进行持续稳定性考察过程中，观察到当时的疫苗效价（疫苗产生预期生物效应的相关参考数据） 呈现下降趋势。作为前瞻性的预防性措施，当时赛诺菲决定暂时停止这些疫苗在中国的供应和销售。 目前赛诺菲方面对第一财经记者表示，2025-2026年流感季流感疫苗生产过程中，公司优化了免疫原性 和产品稳定性评估，于2024年12月完成了原液试生产，并进行了持续的研究和测试，所有结果均证明效 价稳定。 在中国市场，流感疫苗生产厂商数量众多，行业竞争日趋激烈，摆在流感疫苗企业面前的挑战是，长期 以来，中国的流感疫苗接种率处于个位数徘徊。2024年以来，一些流感疫苗厂商相继宣布对流感疫苗进 行降价。 赛诺菲方面表示，部分关键物料从国外进口，考虑到汇率及生产成本等诸多因素，公司不对流感疫苗产 品的价格做出调整。 赛诺菲四价流感疫苗暂停在华销售九个多月后，目前已在重启。 6月13日，赛诺菲宣布，公司针对2025-2026年流感季的四价流感病毒裂解疫苗已获得中国药监局批签发 放行。 接种流感疫苗是预防流感有效手段，但流感病毒毒株每 ...

6月13日，赛诺菲中国宣布，公司针对2025-2026年流感季的四价流感病毒裂解疫苗已获得国家药品监督 管理局批签发放行。(第一财经) ...

Sanofi (NASDAQ:SNY) Goldman Sachs 46th Annual Global Healthcare Conference Call June 10, 2025 4:00 PM ET Company Participants Brian Foard - Executive VP & Head of Specialty Care Conference Call Participants James Patrick Quigley - Goldman Sachs Group, Inc., Research Division James Patrick Quigley Excellent. So welcome, everybody. I'm James Quigley from Goldman Sachs. I'm the European pharma analyst, and it's a pleasure to welcome you all to this session with Sanofi. We're joined today by the Head of Special ...

The Food and Drug Administration on Monday approved Merck's shot designed to protect infants from respiratory syncytial virus during their first season of the virus, bringing to market a rival to a similar treatment from Sanofi and AstraZeneca.The decision will allow the company to launch the drug, which will be marketed as Enflonsia, ahead of the RSV season that typically kicks off around fall and winter and lasts through the spring. Merck said in a release that it expects orders for the shot to begin in J ...

NEW YORK, June 7, 2025 /PRNewswire/ -- Pomerantz LLP is investigating claims on behalf of investors of Sanofi ("Sanofi" or the "Company") (NASDAQ: SNY). Such investors are advised to contact Danielle Peyton at [email protected] or 646-581-9980, ext. 7980.  The investigation concerns whether Sanofi and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices. [Click here for information about joining the class action] On May 30, 2025, Sanofi issued a pres ...

NEW YORK, June 06, 2025 (GLOBE NEWSWIRE) -- Pomerantz LLP is investigating claims on behalf of investors of Sanofi (“Sanofi” or the “Company”) (NASDAQ: SNY).   Such investors are advised to contact Danielle Peyton at newaction@pomlaw.com or 646-581-9980, ext. 7980.    The investigation concerns whether Sanofi and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices.  [Click here for information about joining the class action] On May 30, 2025, Sanofi ...

Sanofi Launches 2025 Global Employee Stock Purchase Plan Paris, June 5, 2025. Sanofi’s global employee shareholder plan, Action 2025, opens on June 10, 2025, to around 70,000 employees in 55 countries. Now in its 11th year, the program demonstrates the ongoing commitment of Sanofi and its Board of Directors to involve employees in the company’s growth and results. In 2024 alone, more than 32,000 Sanofi employees - 40% of the total workforce, chose to invest in the company through the program. Today, nearly ...

Key Takeaways Sanofi's rilzabrutinib receives FDA orphan drug designation for SCD, its fourth such indication. Preclinical data show rilzabrutinib reduced vaso-occlusion and inflammation in SCD mouse models. Rilzabrutinib is also under FDA review for ITP, with a decision expected by August 29, 2025.Sanofi (SNY) announced that the FDA has granted orphan drug designation to its investigational BTK inhibitor, rilzabrutinib, for sickle cell disease (SCD). The candidate exerts its effects through multi-immune ...

ASCO: new Sarclisa data support subcutaneous administration with on-body injector New data from two clinical studies demonstrated that Sarclisa administered subcutaneously via an investigational on-body injector shortened treatment time to minutes with similar efficacy and safety compared to intravenous infusionStudies used Enable Injections’ enFuse® on-body injector, an automated hands-free injectorData will form the basis of global regulatory submissions across all currently approved lines of treatment P ...