赛诺菲将以11.5亿美元现金收购Vicebio。(智通财经) ...

智通财经7月22日电，赛诺菲将以11.5亿美元现金收购Vicebio。 ...

赛诺菲将以11.5亿美元的总预付款收购生物技术公司Vicebio。 ...

Core Viewpoint - Sanofi has announced the acquisition of Vicebio Ltd, enhancing its respiratory vaccines pipeline with a focus on developing combination vaccines for respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) [1][2][5] Group 1: Acquisition Details - The acquisition involves an upfront payment of $1.15 billion, with potential milestone payments of up to $450 million based on development and regulatory achievements [5] - The transaction is expected to close in Q4 2025, pending regulatory approvals [5] Group 2: Technology and Product Pipeline - Vicebio's 'Molecular Clamp' technology stabilizes viral proteins, allowing for quicker development of fully liquid combination vaccines that can be stored at standard refrigeration temperatures (2–8°C) [3][4] - Vicebio's pipeline includes VXB-241, a bivalent vaccine candidate for RSV and hMPV currently in exploratory phase 1 study, and VXB-251, a preclinical trivalent vaccine candidate targeting RSV, hMPV, and parainfluenza virus Type 3 (PIV3) [4] Group 3: Strategic Importance - The acquisition allows Sanofi to expand its offerings in the respiratory vaccines space, providing increased options for physicians and patients by adding a non-mRNA vaccine to its pipeline [2] - Sanofi aims to leverage Vicebio's technology to develop next-generation combination vaccines that could protect older adults against multiple respiratory viruses with a single immunization [4]

Core Viewpoint - Sanofi China announced that its candidate 21-valent pneumococcal polysaccharide conjugate vaccine (referred to as "PCV21 vaccine") developed in collaboration with SK Bioscience has received approval from the National Medical Products Administration (NMPA) to initiate clinical research [1] Group 1 - The PCV21 vaccine is the world's first candidate product for a 20-valent or higher pneumococcal polysaccharide conjugate vaccine to enter Phase III clinical trials for infants and young children [1] - The vaccine has already conducted corresponding Phase III clinical trials in various populations globally prior to this approval [1]

Core Viewpoint - Sanofi has successfully completed the acquisition of Blueprint Medicines, enhancing its portfolio with a commercialized medicine and a promising pipeline focused on systemic mastocytosis and other KIT-driven diseases [1][6]. Group 1: Acquisition Details - The acquisition includes Ayvakit/Ayvakyt (avapritinib), the only approved medicine for advanced and indolent systemic mastocytosis in the US and EU [3][10]. - Sanofi also acquired elenestinib, a next-generation investigational medicine for systemic mastocytosis, currently undergoing a phase 2/3 clinical study [4]. - Additionally, BLU-808, an investigational oral KIT inhibitor, was part of the acquisition, targeting a range of inflammatory diseases [5]. Group 2: Financial Aspects - The tender offer for Blueprint's shares was completed on July 17, 2025, with all conditions satisfied [6]. - Sanofi financed the acquisition through cash on hand and proceeds from commercial paper issuances, indicating it will not significantly impact the company's financial guidance for 2025 [7]. - The acquisition is expected to be immediately accretive to gross margin and business operating income, as well as EPS after 2026 [7]. Group 3: Market Impact - Following the acquisition, Blueprint common stock will cease trading on the NASDAQ Global Select Stock Market as of July 18, 2025 [9]. - All shares not validly tendered will convert to a cash payment of $129.00 per share, plus potential contingent payments of up to $6.00 per share based on milestone achievements [8].

Core Points - Sanofi has extended its tender offer to acquire all outstanding shares of Blueprint Medicines Corporation at a price of $129.00 per share in cash, plus contingent rights for additional payments of up to $6.00 per share based on specified milestones [1][2] - The expiration date for the tender offer has been moved to 17:00 EDST on July 17, 2025, from the previous date of July 16, 2025 [2] - As of July 16, 2025, approximately 29,742,419 shares, or 45.85% of Blueprint's total outstanding shares, have been validly tendered, with an additional 23,400,152 shares tendered by notice of guaranteed delivery, representing 36.08% of the outstanding shares [3] Offer Details - The tender offer is subject to conditions outlined in the offer to purchase, including the requirement for a majority of Blueprint's outstanding shares to be tendered [5] - The offer is being managed by Rothko Merger Sub, Inc., a wholly owned subsidiary of Sanofi, and Innisfree M&A Incorporated is acting as the information agent for the offer [4][6] Company Background - Sanofi is a research and development-driven biopharmaceutical company focused on improving lives through innovative medicines and vaccines, leveraging its understanding of the immune system [7]

赛默飞世尔科技公司7月16日宣布，将扩大与赛诺菲的战略合作伙伴关系，以扩大美国药品生产规模。 交易条款未披露。根据协议，赛默飞将收购赛诺菲位于美国新泽西州里奇菲尔德的无菌生产基地，并将 继续为赛诺菲生产一系列疗法。赛默飞还将扩大该基地的使用范围，以满足制药和生物技术客户对美国 生产能力日益增长的需求。此次交易预计将于2025年下半年完成，但需满足惯例成交条件。(智通财经) ...

Core Insights - Sanofi has received FDA fast-track designation for its gene therapy SAR446597, aimed at treating geographic atrophy (GA) due to age-related macular degeneration (AMD) [1][7] - The fast-track status is designed to expedite the development and review of drugs addressing serious conditions and unmet medical needs [2] - GA affects approximately 1 million people in the U.S. and over 5 million globally, leading to irreversible vision loss [3] Drug Development - SAR446597 is an investigational gene therapy that aims for long-lasting complement inhibition with a single injection, contrasting with current treatments requiring frequent injections [4][7] - The therapy targets two key complement cascade pathways, potentially offering durable treatment for GA [4][5] - Sanofi plans to initiate a phase I/II study to evaluate the safety, tolerability, and efficacy of SAR446597 in GA patients [7][8] Market Context - Apellis Pharmaceuticals' Syfovre is currently the market leader in GA treatment, holding over 60% market share and generating $611.9 million in sales in 2024 [9] - Astellas Pharma's Izervay is also FDA-approved for treating GA secondary to AMD [10] Stock Performance - Year-to-date, Sanofi's shares have declined by 0.2%, while the industry has seen a slight increase of 0.4% [6]

Core Viewpoint - Sanofi showcased its commitment to the Chinese market and patients at the third China International Supply Chain Promotion Expo, emphasizing its achievements in high-quality manufacturing, supply chain innovation, and patient health empowerment [1][4]. Group 1: Company Commitment and Achievements - Sanofi has been deeply rooted in the Chinese market for over 40 years, establishing a comprehensive ecological value chain that includes local R&D, manufacturing, and patient services [4]. - This year marks the 30th anniversary of Sanofi's local manufacturing in China, highlighting its ongoing commitment to enhancing high-quality production capabilities and responding to market needs [4]. - The company aims to support the "Healthy China" vision by making innovative drugs and vaccines accessible to a larger population [4][6]. Group 2: Innovations and Product Development - At the expo, Sanofi presented a "traceability journey" of flu vaccine production, showcasing its global collaboration and local supply chain advantages [5]. - The company highlighted nine breakthrough products across key disease areas, including immunology, respiratory, cardiovascular, transplantation, oncology, and rare diseases, demonstrating a comprehensive "immunization innovation chain" [5]. - Sanofi has established four R&D centers in Beijing, Shanghai, Suzhou, and Chengdu, contributing to over 90% of its global synchronized development projects, including 12 potential blockbuster products [5]. Group 3: Focus on Healthcare Accessibility - In response to national policies aimed at improving drug accessibility, Sanofi is committed to promoting equitable healthcare services and building a future where everyone can enjoy health benefits [6].