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全球新药研发市场变天!哈佛最新报告:中国生物技术有望超越美国
Di Yi Cai Jing·2025-06-06 05:26

Group 1 - The balance of global biotechnology power is shifting, with China rapidly emerging as a potential leader in original innovation, particularly in drug development [1][2] - A recent report from Harvard's Belfer Center indicates that China has the best chance of surpassing the US in biotechnology, despite the US's current lead in key technology sectors [2] - China's advantages in biotechnology stem from its dominant position in pharmaceutical manufacturing and a larger talent pool compared to the US [2] Group 2 - China's drug approval process is more efficient and flexible than that of the US, contributing to a higher number of clinical trials and a significant increase in patent filings [2] - Major pharmaceutical companies from the US and Europe have invested billions in acquiring Chinese-developed drugs, indicating growing interest in China's biotech sector [2][3] - BioNTech's recent acquisition of a drug from a Chinese company for over $10 billion highlights the value of Chinese innovations in the global market [3] Group 3 - The US biotechnology sector is experiencing layoffs and project stagnation due to funding cuts, contrasting with the rising interest in Chinese biotech companies [4] - Goldman Sachs has released a report indicating that China's innovative capabilities in biotechnology are gaining global recognition, with expectations for several leading companies to reach breakeven by 2025/2026 [4] - China is becoming a hub for the development of innovative drugs like antibody-drug conjugates (ADCs), which are in high demand from multinational pharmaceutical companies [4] Group 4 - Chinese biopharmaceutical companies listed in the US have seen significant stock price increases, reflecting renewed market interest [5] - The Hong Kong stock market is also witnessing a resurgence in biopharmaceutical demand, with a major new share issuance by Kelun-Biotech [5] - For Chinese biopharmaceutical companies to succeed globally, they must adapt to various regulatory requirements and leverage global clinical resources for cost efficiency [5]