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体内CAR-T:全球竞赛已打响,关注云顶新耀和石药集团
CSPC PHARMACSPC PHARMA(HK:01093)2025-07-02 01:24

Summary of Key Points from the Conference Call Industry Overview - The conference call discusses the advancements in in vivo CAR-T technology, highlighting the global competition in this field, particularly focusing on YunTing Xinyao and Shiyao Group as key domestic players [1][2]. Core Insights and Arguments - Acquisition Activity: AbbVie’s acquisition of Capstan for $2.1 billion marks a significant event in the industry, indicating strong interest and investment in in vivo CAR-T technology [1][2]. - Market Potential: Current autologous CAR-T therapies have limited global sales of less than $4.5 billion due to high costs. In vivo CAR-T aims to reduce costs and improve accessibility, with predictions suggesting costs could be reduced by an order of magnitude [2][4]. - mRNA Platform Advantages: The mRNA platform has demonstrated safety and efficacy, particularly validated through COVID-19 vaccine development. It is expected to be a breakthrough point for in vivo CAR-T therapies [1][2][7]. - Clinical Developments: AstraZeneca's P3B3A CAR-T technology has received FDA Phase I approval, targeting multiple myeloma and autoimmune diseases, while Interose has initiated Phase I trials in Australia and Europe [5][6]. Additional Important Content - LNP Delivery System: The LNP delivery system is crucial for the effectiveness of in vivo CAR-T therapies, requiring efficient delivery to the spleen and rapid degradation for safety [3][10]. - Research Progress: Capstan's preclinical studies show no liver toxicity at doses ranging from 0.1g to 2mg, indicating good safety profiles. YunTing Xinyao has achieved a single conversion rate exceeding 60% in monkey experiments [11][12]. - Strategic Advantages of YunTing Xinyao: The company benefits from a complete mRNA platform, a strong research team, and significant annual investments in R&D, enabling them to make breakthroughs in antigen design and mRNA sequence optimization [13]. - Shiyao Group's Developments: The group has made significant strides in the mRNA platform, obtaining three BCMA CAR-T product approvals for multiple myeloma and autoimmune diseases, laying a solid foundation for future developments in in vivo CAR-T [14]. - Upcoming Data Releases: Key human data related to both lentiviral vectors and LNP-packaged mRNA CAR-T therapies are expected to be released between the second half of 2025 and the first half of 2026, which could catalyze further advancements in the field [15].