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시장보고서
상품코드
1900018
고분자 원료의약품 CDMO 시장 규모, 점유율, 성장 분석 : 서비스별, 원료원별, 최종사용자별, 지역별 - 업계 예측(2026-2033년)Large Molecule Drug Substance CDMO Market Size, Share, and Growth Analysis, By Service (Contract Manufacturing, Contract Development), By Source (Mammalian, Microbial), By End-user, By Region - Industry Forecast 2026-2033 |
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세계의 고분자 원료의약품 CDMO 시장 규모는 2024년에 128억 8,000만 달러로 평가되었으며, 2025년 139억 9,000만 달러에서 2033년까지 270억 6,000만 달러로 성장할 전망입니다. 예측 기간(2026-2033년) 동안 CAGR은 8.6%로 예측됩니다.
고분자 원료의약품 CDMO 세계 시장은 바이오의약품 승인 증가, 감염성 질환 발생률 증가, 신규 치료제에 대한 수요 증가에 힘입어 성장하고 있습니다. 제약 및 바이오테크 기업들이 첨단 기술에 대한 투자와 CDMO와의 협력을 강화하면서 고품질, CGMP 준수 제조 서비스에 대한 수요가 급증하고 있으며, 특히 팬데믹 기간 동안 그 중요성이 더욱 부각되고 있습니다. 효과적인 백신과 단클론항체 개발의 시급성은 원료의약품(DS) 및 제제(DP) 개발에서 CDMO의 중요한 역할을 강조하며, 제약 생태계 내 지역 협력의 중요성을 강조하고 있습니다. 고분자 화합물의 복잡성으로 인한 비용 효율성 및 효율성의 문제는 있지만, 안정성과 유효성을 높이는 캡슐화 등 혁신적인 기술이 등장하면서 CDMO는 의약품 개발 분야에서 없어서는 안 될 존재로 자리매김하고 있습니다.
세계 고분자 원료의약품 CDMO 시장 촉진요인
기업들이 바이오의약품 및 바이오시밀러 개발에 막대한 투자를 한 결과, 고분자 원료의약품 위탁개발생산기관(CDMO)에 대한 수요가 크게 증가했습니다. 현재 탐색 단계에 있는 잠재적 치료 후보물질의 대부분은 펩타이드, 단백질, 단클론항체 등 생물학적 제제로 구성되어 있습니다. 바이오제약 기업의 연구개발 투자가 급증하면서 혁신적인 생물학적 제제 개발 및 파이프라인을 통한 진전이 이루어지고 있습니다. 이러한 요인들이 복합적으로 작용하여 고분자 의약품용 CDMO 시장 확대를 주도하고 있습니다.
세계 고분자 원료의약품 CDMO 시장 억제요인
세계 고분자 원료의약품 CDMO 시장은 고분자 특성 평가에 따른 고유한 복잡성으로 인해 심각한 도전에 직면해 있습니다. 바이오의약품 분야에서는 안정성, 순도, 기능 등 중요한 파라미터를 평가하기 위해 철저한 특성 평가가 필수적입니다. 효과적인 구조 검증을 위해서는 다양한 저해상도 및 고해상도 기술의 통합이 필요합니다. 또한, 재조합 합성 과정에서 고분자에서 다양한 번역 후 변형(PTM)이 발생하는 경우가 많아 특성 평가가 더욱 복잡해집니다. 이러한 도전에도 불구하고, R&D 및 제품 혁신에 대한 투자 증가는 시장을 뒷받침하고 있으며, 이 분야의 발전을 지속적으로 추진하고 있습니다.
세계 고분자 원료의약품 CDMO 시장 동향
세계 고분자 원료의약품 CDMO 시장은 바이오의약품의 수요 증가와 제조의 복잡성 증가에 힘입어 변화의 길을 걷고 있습니다. 기존 저분자 의약품과 달리 대형 바이오의약품은 특히 종양학 및 맞춤 의료 분야에서 소규모 배치 크기와 고유한 제형을 수반하는 전문적 제조가 필요합니다. 이러한 환경에서는 자체 제조 자원이 없는 혁신적인 스타트업 기업의 성장이 촉진되고, 유연한 CDMO(Contract Development Manufacturing Organization)를 통한 맞춤형 솔루션 제공이 중요시되고 있습니다. 규제 기준이 강화됨에 따라 CDMO는 봉쇄 방법을 강화하고, 고활성 원료의약품(API)의 요구사항에 대응하기 위한 운영 전략에 대한 적응을 요구받고 있으며, 급속히 발전하고 복잡해지는 시장에서의 역할을 확고히 하고 있습니다.
Global Large Molecule Drug Substance CDMO Market size was valued at USD 12.88 Billion in 2024 and is poised to grow from USD 13.99 Billion in 2025 to USD 27.06 Billion by 2033, growing at a CAGR of 8.6% during the forecast period (2026-2033).
The global market for large molecule drug substance CDMOs is driven by the rising approvals of biologics, escalating incidences of infectious diseases, and an increasing demand for novel therapeutics. As pharmaceutical and biotech companies invest more in advanced technologies and collaboration with CDMOs, the need for high-quality, CGMP-compliant manufacturing services has surged, particularly highlighted during the pandemic. The urgency for effective vaccines and monoclonal antibodies has showcased the critical role of CDMOs in drug substance (DS) and drug product (DP) development, emphasizing the importance of regional partnerships within the pharmaceutical ecosystem. Despite challenges in affordability and efficiency due to the complexity of large molecules, innovative techniques like encapsulation are emerging to enhance stability and efficacy, positioning CDMOs as essential players in the drug development landscape.
Top-down and bottom-up approaches were used to estimate and validate the size of the Global Large Molecule Drug Substance CDMO market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Global Large Molecule Drug Substance CDMO Market Segments Analysis
Global Large Molecule Drug Substance CDMO Market is segmented by Service, Source, End-user and region. Based on Service, the market is segmented into Contract Manufacturing and Contract Development. Based on Source, the market is segmented into Mammalian, Microbial and Others. Based on End-user, the market is segmented into Biotech Companies, CRO and Others. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Driver of the Global Large Molecule Drug Substance CDMO Market
The demand for large molecule drug substance contract development and manufacturing organizations (CDMOs) has significantly increased due to substantial investments made by companies in the development of biologics and biosimilars. A large portion of potential therapeutic candidates currently in the discovery phase consists of biologics, including peptides, proteins, and monoclonal antibodies. This surge in investment in research and development by biopharmaceutical firms has led to a growing number of innovative biologics being developed and advanced through the pipeline. As a result, these factors collectively drive the expansion of the CDMO market for large molecule drugs.
Restraints in the Global Large Molecule Drug Substance CDMO Market
The Global Large Molecule Drug Substance CDMO market faces significant challenges due to the inherent complexity associated with characterizing large molecules. In the biopharmaceutical sector, thorough characterization is essential for assessing vital parameters such as stability, purity, and function. Achieving effective structural validation necessitates the integration of various low- and high-resolution techniques. Moreover, the recombinant synthesis process often leads to various post-translational modifications (PTMs) in large molecules, complicating their characterization further. Despite these hurdles, the market is supported by increasing investments in research and development as well as product innovation, which continue to drive advancements in the field.
Market Trends of the Global Large Molecule Drug Substance CDMO Market
The Global Large Molecule Drug Substance CDMO market is undergoing a transformative shift driven by the rising demand for biopharmaceuticals and the complexities of their production. Unlike traditional small-molecule drugs, large biologics require specialized manufacturing that often involves smaller batch sizes and unique formulations, particularly in oncology and personalized medicine. This environment has spurred the growth of innovative startups that lack the resources for in-house manufacturing, emphasizing the need for agile contract development and manufacturing organizations (CDMOs) to offer tailored solutions. As regulatory standards tighten, these CDMOs must enhance containment methods and adapt operational strategies to meet the demands of high-potency active pharmaceutical ingredients (APIs), solidifying their role in a market characterized by rapid advancements and increasing complexity.