生物技术

AI Integration in Biotechnology Industry Reaches a New Turning Point in 2025

Editor
7 分钟阅读

In 2025, the biotechnology industry is reaching a new turning point through the full-fledged integration with artificial intelligence. The global bio-AI market is projected to grow by 33%, from $3.9 billion in 2024 to $5.2 billion in 2025, and is expected to reach $28.5 billion by 2030 with an average annual growth rate of 28.4%. This rapid growth is driven by the accelerated digital healthcare transition post-COVID-19 pandemic, increased demand for personalized medicine, and above all, the remarkable advancement of AI technology.

AI Integration in Biotechnology Industry Reaches a New Turning Point in 2025

One of the notable trends in 2025 is the commercial success of ‘AI-based drug development platforms.’ The UK-based Exscientia announced that its first AI-developed drug candidate showed positive results in Phase 2 clinical trials, reducing the development period by 40% compared to traditional processes. Similarly, U.S. company Recursion Pharmaceuticals has five drug candidates discovered through its AI platform currently undergoing clinical trials, with two expected to announce significant results in the second half of 2025. These achievements demonstrate to biotech investors that AI-based drug development is no longer a future technology but a current business reality.

The Korean biotech industry is actively responding to this global trend. Samsung Biologics, headquartered in Seongnam, Gyeonggi Province, announced a 120 billion KRW investment in March 2025 to establish an AI-based biopharmaceutical development platform. This strategy is linked to Samsung Group’s AI strategy, combining Samsung SDS’s AI capabilities with Samsung Biologics’ bio-manufacturing expertise to build a next-generation biopharmaceutical development ecosystem. Additionally, Celltrion, based in Incheon, began operating its AI-based antibody design platform in the fourth quarter of 2024, with its first antibody candidate expected to enter preclinical trials in the first half of 2025.

Technological Innovations and Market Dynamics in AI Drug Development

The core of AI-based drug development technology is learning vast biological data to predict and design new drug candidates. Notably, advancements in protein structure prediction technology are bringing innovation to this field. DeepMind’s AlphaFold, which has released a database of over 200 million protein structures, is available for free to researchers worldwide, rapidly advancing drug target discovery. As of 2025, there are approximately 3,400 drug development projects worldwide utilizing AlphaFold data, with about 15% entering the clinical trial phase.

Genentech, a Roche subsidiary based in San Francisco, California, announced in February 2025 that it discovered a new anticancer drug candidate through its AI-based antibody-drug conjugate (ADC) development platform. This platform uses machine learning algorithms to optimize antibody binding sites and predict drug delivery efficiency, showing a 30% improvement in therapeutic effects compared to existing methods. Roche plans to build more than 10 ADC pipelines over the next three years based on this technology.

In contrast, Johnson & Johnson, headquartered in New Jersey, is taking a somewhat conservative approach. The company prioritizes using AI technology for drug repurposing and clinical trial optimization rather than new drug discovery. The head of J&J’s innovation division stated, “AI technology provides clear value in drug development, but a phased approach is needed in terms of regulatory environment and safety verification.” This difference in approach highlights the varying views on AI adoption strategies among major pharmaceutical companies.

In the AI drug development field, the use of ‘generative AI’ is particularly noteworthy. Beyond simply analyzing existing data, technology that generates entirely new molecular structures is being commercialized. Mila AI, based in Cambridge, UK, announced that a new antibiotic candidate designed with generative AI showed a 99.7% inhibitory effect against multidrug-resistant bacteria. This is more than ten times the improvement compared to existing antibiotics, offering a new breakthrough in addressing antibiotic resistance issues.

Digital Transformation and Competitive Dynamics in Biomanufacturing

AI technology is driving innovation not only in drug development but also in biomanufacturing processes. AI adoption is accelerating at every stage of biopharmaceutical production, including cell line development, culture condition optimization, and quality control. Samsung Biologics announced the full implementation of an AI-based smart manufacturing system at its fourth plant in Songdo, Incheon, in 2025. This system analyzes real-time process data to automatically adjust optimal production conditions, expected to improve yield by 15-20% compared to existing methods.

The status of Korean companies in the global biomanufacturing market is also rising significantly. Samsung Biologics recorded sales of 2.8 trillion KRW in 2024, a 24% increase from the previous year, and aims to surpass 3.3 trillion KRW in 2025. The productivity improvement from AI technology adoption is a major driver of sales growth. Celltrion also achieved a record high in biosimilar sales, reaching 1.95 trillion KRW in 2024, and plans to secure new growth drivers by expanding its AI-based drug pipeline in 2025.

Moderna, headquartered in Cambridge, Massachusetts, is developing next-generation vaccines and therapeutics through the convergence of mRNA technology and AI. The company announced that its RSV vaccine, developed through an AI-based mRNA sequence design platform, induced more than twice the immune response compared to existing vaccines in Phase 2 clinical trials. Based on these results, Moderna plans to add more than 20 new mRNA therapeutic candidates to its pipeline in the second half of 2025. Particularly in the field of personalized cancer vaccines, the accuracy of tumor antigen prediction using AI technology reaches 85%, increasing the potential for commercialization.

Another key aspect of AI adoption in biomanufacturing is supply chain optimization. Efforts to address the vulnerabilities of the global biopharmaceutical supply chain exposed by the COVID-19 pandemic through AI technology are in full swing. Roche, headquartered in Basel, Switzerland, announced the implementation of an AI-based demand forecasting system at its global production facilities in 2025. This system comprehensively analyzes disease incidence rates, prescription patterns, and inventory levels in each country to establish optimal production plans, expected to reduce inventory costs by 30% while significantly enhancing supply stability.

These changes are also altering the criteria for assessing the competitiveness of biomanufacturers. In the past, simple production scale and cost competitiveness were the main factors, but now AI technology capabilities, data analysis skills, and digital infrastructure levels are emerging as new differentiators. Particularly, Asian biomanufacturers are actively investing in this digital transformation, bringing new changes to the traditionally Western-centric biomanufacturing ecosystem.

From an investment perspective, venture investment in the bio-AI sector in 2025 is expected to increase by 45% from the previous year, reaching $12.7 billion. Notably, late-stage investments after Series B account for 62% of the total, indicating that AI biotech companies are moving beyond the proof-of-concept (PoC) stage and approaching commercialization. In Korea, support for AI biotech startups is expanding through the government’s K-Bio Grand Challenge program, with a total investment of 80 billion KRW planned for 2025.

However, despite these growth prospects, the bio-AI industry faces significant challenges. The biggest issue is regulatory uncertainty. The U.S. FDA released a draft guideline for AI-based drug development at the end of 2024, but specific approval criteria remain unclear. The European Medicines Agency (EMA) is in a similar situation, requiring consensus between the industry and regulatory authorities on the methodology for evaluating the safety and efficacy of AI-developed drugs. The Korean Ministry of Food and Drug Safety also plans to release AI drug development guidelines in the first half of 2025, but harmonizing with global standards remains a critical task.

Data quality and accessibility issues also remain challenges to be addressed. The performance of AI models critically depends on the quality and quantity of training data, yet high-quality data in the bio field is still scarce and access is limited. Particularly, the lack of data on rare diseases or specific ethnic groups can lead to bias in AI models, making the construction of inclusive and diverse datasets an urgent task. To address this, global efforts to build bio data-sharing platforms are actively underway, with Korea participating through its National Bio Big Data project.

In conclusion, the AI integration in the biotechnology industry in 2025 has moved beyond the experimental stage and entered a full-fledged commercialization trajectory. Concrete achievements are emerging in various areas, including innovation in drug development processes, improved biomanufacturing efficiency, and the realization of personalized medicine. Korean biotech companies are accelerating AI technology adoption in line with global trends, establishing new competitive advantages through the combination of manufacturing capabilities and AI technology. However, resolving challenges such as regulatory clarity, data accessibility improvement, and workforce development is essential for these innovations to lead to sustainable growth. For investors, it is crucial to select companies with both technological capabilities and regulatory responsiveness, with particular attention to the global competitiveness enhancement of Korean biotech companies.

—

**Disclaimer**: This analysis is based on publicly available information and should not be interpreted as investment advice or a trading signal. All investment decisions should be made at one’s own discretion and responsibility, with full consideration of the potential risks of loss.

Editor

Leave a Comment

Related Articles

生物技术产业的新转折点:2026年AI融合与个性化治疗市场趋势分析

2026年,生物技术产业正经历历史上最为动态的变化,三大趋势同时进行:与人工智能的融合、个性化治疗的商业化以及下一代生物制造平台的普及。根据麦肯锡的最新报告,全球生物技术市场在2026年已增长至1.24万亿美元,比前一年增长了18.5%。尤其值得注意的是,基于AI的新药开发市场单独形成了890亿美元的规模,占整个生物技术投资的32%。这种增长不仅仅是技术进步,还意味着整个生物产业的范式转变,传统制药公司与新兴生物技术企业之间的界限正在迅速模糊。 韩国的生物技术生态系统在2026年表现尤为显著。位于仁川松岛的三星生物制剂公司在今年第一季度实现了8,950亿韩元的销售额,同比增长24%,这大大提升了韩国企业在全球CDMO(合同开发与制造组织)市场的地位。特别是三星生物制剂公司最近与美国Moderna签订的mRNA疫苗生产合同预计将在未来五年内带来约2万亿韩元的销售额。同时,总部位于仁川的Celltrion在生物仿制药领域保持着独特的地位,2026年上半年实现了1.32万亿韩元的销售额。这是因为其抗癌生物仿制药产品在欧洲和美国的市场份额持续扩大。 AI与生物技术的融合是2026年最受关注的趋势之一,推动了新药开发过程的全面创新。自英国伦敦的DeepMind的AlphaFold技术商业化以来,蛋白质结构预测领域取得了惊人的进展。目前,全球主要制药公司的78%已采用基于AI的新药开发平台,通过此平台将平均新药开发周期从原来的12-15年缩短至8-10年。位于美国加州旧金山的Genentech宣布,通过AI设计的抗体平台,仅在2026年就获得了15个新的管线。这种基于AI的方法不仅提高了开发速度,还使得对以前不可能的靶点的药物开发成为可能。 个性化治疗市场的爆炸性增长 Kymriah和Breyanzi是由不同公司开发的CAR-T疗法,用于特定的复发性或难治性B细胞恶性肿瘤。FDA资料显示,Kymriah属于Novartis,Breyanzi属于Bristol Myers Squibb旗下的Juno Therapeutics。CAR-T治疗也存在严重风险,因此不能概括为能够治愈所有血液癌症。 EDIT-101在14名LCA10患者中开展的是1/2期试验。Editas的申报文件称,在2022年11月的分析中,14人中有3人达到公司设定的复合反应标准,公司于2023年1月暂停继续招募。随后发表的2024年同行评议论文报告,14人中有11人在四项结局指标中的至少一项达到具有临床意义的改善,6人在至少两项指标上达到这一标准。由于不同指标的结果并不相同,不能把该研究表述为2期或3期试验,也不能概括为73%或87%的统一视力改善率。 亚洲地区,特别是中国和日本的个性化治疗市场增长显著。总部位于中国上海的WuXi AppTec通过个性化细胞治疗CDMO业务在2026年上半年实现了28亿美元的销售额,同比增长45%。在日本,京都大学iPS细胞研究所相关的多个生物创业公司在iPS细胞基础的再生治疗开发中取得了显著成果。特别是位于日本大阪的Healios宣布,其利用iPS细胞来源的神经干细胞治疗中风的药物HLCN061在二期临床试验中确认了显著效果。 生物制造平台的创新与竞争格局 生物制造领域在2026年经历了自动化、连续生产和数字孪生技术的引入带来的根本性变化。从传统的批量生产方式向连续生产方式的转变正在加速,通过此方式生产效率平均提高了40%,成本降低了25%。总部位于美国新泽西州的强生公司Janssen部门在比利时Beerse的新设施中引入了连续生产方式,将单克隆抗体生产成本降低了35%。该设施具备每年生产2,000公斤抗体的能力,在30%更少的空间内实现了与现有设施相同的生产量。 数字技术在生物制造中的引入在质量控制和工艺优化方面带来了创新性变化。总部位于德国达姆施塔特的Merck KGaA在其生物制造设施中引入了基于AI的工艺分析技术(PAT,Process Analytical Technology),实现了实时质量监控和预测性维护。通过此技术,批次失败率从原来的3.2%大幅降低至0.8%,整体生产效率提高了28%。在韩国,三星生物制剂在仁川第三工厂引入的智能工厂系统备受关注。该系统整合了IoT传感器、AI分析和自动化机器人,建立了最小化人类干预的无人生产线,从而提高了22%的生产力,并减少了85%的人为错误。 生物制造领域的竞争格局在2026年变得更加激烈。现有的大型CDMO企业与新兴平台企业之间的竞争加剧,特别是下一代治疗类型的生产能力成为核心竞争要素。总部位于瑞士巴塞尔的Lonza大幅扩展了mRNA、细胞与基因治疗以及ADC(抗体-药物偶联物)的生产能力,预计在2026年仅此领域就将实现45亿美元的销售额。这相当于总销售额的67%,反映了下一代治疗市场的快速增长。 亚洲地区作为生物制造中心的地位也大大增强。特别是新加坡在政府的积极支持下建立了生物制造集群,截至2026年,已有12个主要生物制造设施在运营。新加坡政府宣布计划到2030年在生物制造领域投资总计200亿美元,以此推动成为亚太地区的生物制造中心。韩国也通过K-生物带项目在仁川、五松和大邱地区建立了生物集群,截至2026年,已有340家生物企业集中于此。 从生物技术产业的投资趋势来看,2026年是以选择性投资和战略合作伙伴关系为主的年份。根据PitchBook的分析,2026年上半年全球生物技术投资规模为340亿美元,同比下降8%,但平均投资规模为1.23亿美元,增长了23%。这表明投资者更加关注拥有成熟技术和明确商业化路径的企业。特别是对拥有AI基础新药开发平台的企业的投资集中,仅此领域就投入了89亿美元。…

合成生物学重塑医疗产业:2025年生物技术创新的前沿

合成生物学技术正在从根本上改变传统制药开发的范式。从个性化疗法到生物燃料,编程生命体的技术在2025年已进入商业化阶段,创造了规模达数十万亿韩元的新市场。

合成生物学革命:2026年生物技术产业的新范式

合成生物学正在重新定义传统生物技术产业的边界,截至2026年,在从药品到材料的各个领域都展现出商业成果。预计全球合成生物学市场将以年均25%的速度增长,到2030年达到850亿美元的规模,包括韩国在内的主要国家的投资竞争日趋激烈。