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市场调查报告书
商品编码
1319192
全球小分子 CDMO 的增长机会Global Small Molecule Contract Development and Manufacturing Organization (CDMO) Growth Opportunities |
通过 Lighthoring 和标靶治疗创造未来增长
CDMO(合同开发和製造组织)是外包药物开发和製造服务的第三方供应商。在小分子药物製造领域,CDMO提供专业的开发和製造服务,现已成为製药行业价值链不可或缺的一部分。
慢性病患病率的不断上升增加了对创新小分子药物的需求。製药行业专注于开发新颖、更有效的靶向疗法,导致产品线不断增长,对创新药物输送方法的需求也不断增长。与此同时,中小型製药公司负责其研发管线中70%以上的药物,但往往缺乏将其临床管线推向市场的专业知识。
Frost & Sullivan 预计,由于对小分子口服固体剂型、标靶药物给药技术、强效和高活性药物以及其他復杂分子的需求不断增加,预测期内将出现持续增长。能够提供技术领先、灵活性、模块化製造专业知识、端到端能力和能力以及创新药物输送技术的 CDMO 将成为首选合作伙伴。为了推动增长,CDMO 将继续优先考虑製造流程各个方面的创新、协作、扩张、自动化和优化。
本报告分析了全球小分子 CDMO 市场。分析期为2021-2028年,其中2022年为基准年,2023-2028年为预测期。根据产品类型,大致分为原料药(API)/药品製造和成品药(FDF)/药品製造。此外,API分为创新药和仿製药,FDF分为口服剂型、半固体/液体剂型和注射剂型。
最重要的是,该报告根据小分子 CDMO 市场不断变化的需求和创新、标靶治疗、高活性 API 和復杂药物的出现,强调了各种规模的进入者的商机。
Right Shoring and Targeted Therapeutics Create Future Growth
CDMOs are third-party vendors that offer outsourced development and manufacturing services for pharmaceutical drugs. In the small molecule manufacturing sector, CDMOs provide expert development and manufacturing services and are now an essential part of the pharmaceutical industry's value chain.
The growing incidence of chronic diseases propels the demand for innovative small-molecule medicines. The pharmaceutical industry's focus on developing novel, more efficacious, and targeted therapies has resulted in increased product pipelines and the need for innovative drug delivery methods. Simultaneously, while small and mid-sized pharma companies are responsible for over 70% of drugs in the R&D pipeline, they often lack the expertise to bring their clinical pipeline to market.
Frost & Sullivan expects sustained growth during the forecast period, driven by increasing demand for small molecules in oral solid formulations, targeted drug delivery technologies, potent and highly potent drugs, and other complex molecules. CDMOs equipped to provide technological leadership, flexibility, expertise for modular manufacturing, end-to-end capabilities and capacities, and innovative drug delivery technologies will likely emerge as the partner of choice. To drive growth, CDMOs will continue prioritizing innovation, collaboration, expansion, automation, and optimization across all aspects of the manufacturing process.
In this report, Frost & Sullivan overviews the global small-molecule CDMO market. The study period is 2021-2028, with 2022 as the base year and 2023-2028 as the forecast period. We segment the study into two main categories based on the product type: active pharmaceutical ingredients (API)/drug substance manufacturing and fixed dosage form (FDF)/drug product manufacturing. Frost & Sullivan segments API further into innovator and generic and FDF into oral, semisolid/liquid, and injectables.
Most importantly, the report highlights opportunities for participants of all sizes based on the evolving needs and innovations in the small-molecule CDMO market, the emergence of targeted therapeutics, highly potent APIs, and complex drugs.