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市場調查報告書
商品編碼
1319192
全球小分子CDMO的成長機會Global Small Molecule Contract Development and Manufacturing Organization (CDMO) Growth Opportunities |
正確的支撐和標靶治療創造未來成長
CDMO(契約開發和製造組織)是外包藥物開發和製造服務的第三方供應商。在小分子藥物製造領域,CDMO提供專業的開發和製造服務,現已成為製藥行業價值鏈不可或缺的一部分。
慢性病患病率的不斷上升增加了對創新小分子藥物的需求。製藥行業致力於開發新穎、更有效的靶向療法,導致產品線不斷成長,對創新藥物輸送方法的需求也不斷成長。與此同時,中小型製藥公司負責其研發管線中70%以上的藥物,但往往缺乏將其臨床管線推向市場的專業知識。
Frost & Sullivan 預計,由於對小分子口服固體劑型、標靶藥物給藥技術、強效和高活性藥物以及其他複雜分子的需求不斷增加,預測期內將出現持續成長。能夠提供技術領先、靈活性、模組化製造專業知識、端到端能力和能力以及創新藥物輸送技術的 CDMO 將成為首選合作夥伴。為了推動成長,CDMO 將繼續優先考慮製造流程各個方面的創新、協作、擴張、自動化和最佳化。
本報告分析了全球小分子 CDMO 市場。分析期為2021-2028年,其中2022年為基準年,2023-2028年為預測期。根據產品類型,大致分為原料藥(API)/藥品製造和成品藥(FDF)/藥品製造。此外,API分為創新藥和學名藥,FDF分為口服劑型、半固體/液體劑型和注射劑型。
最重要的是,本報告根據小分子 CDMO 市場不斷變化的需求和創新、標靶治療、高活性 API 和複雜藥物的出現,強調了各種規模的進入者的商機。
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.