시장보고서
상품코드
1971787

항체약물접합체(ADC) 시장 분석 및 예측 : 유형별, 제품 유형별, 서비스별, 기술별, 용도별, 최종 사용자별, 프로세스별, 단계별, 솔루션별, 모드별(-2035년)

Antibody Drug Conjugate Market Analysis and Forecast to 2035: Type, Product, Services, Technology, Application, End User, Process, Stage, Solutions, Mode

발행일: | 리서치사: Global Insight Services | 페이지 정보: 영문 303 Pages | 배송안내 : 3-5일 (영업일 기준)

    
    
    



※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

항체약물접합체(ADC) 시장은 2024년 210억 달러로 평가되었고, 2034년까지 439억 달러에 이르고 CAGR은 약 7.7%를 나타낼 것으로 예측됩니다. 항체약물접합체(ADC) 시장은 단일클론항체와 세포독성 약물을 조합한 치료제를 포함하여 특정 암세포를 표적으로 하면서 건강한 조직에 대한 손상을 최소화합니다. 이 시장은 표적 암 치료의 진보, 암 이환율 증가, 약물전달 시스템의 기술 혁신에 의해 견인되고 있습니다. 지속적인 임상시험, 규제 당국의 승인, 주요 업계 기업 간의 전략적 제휴가 시장 성장을 더욱 가속화하고 있습니다.

항체약물접합체(ADC) 시장은 표적암 치료와 맞춤형 의료의 진보에 견인되어 견고한 확대를 계속하고 있습니다. 종양학 분야가 최전선에 있으며, 특히 유방암 및 혈액 악성 종양은 미충족 요구가 높기 때문에 주요 초점 영역이 되고 있습니다. 이 분야에서 유방암용 ADC는 유망한 임상 성과를 제공하여 가장 높은 실적을 올리고 있습니다. 혈액종양용 ADC도 혁신적인 작용기전을 살려 그에 이어 성장을 보이고 있습니다. 링커 기술 분야는 ADC의 안정성과 효능을 높이는 데 매우 중요합니다. 절단형 링커는 종양 부위에서 정밀한 약물 방출을 가능하게 하고, 성능면에서 우위성을 나타내고 있습니다. 비절단형 링커도 치료 지수 개선에 의해 주목을 받고 있습니다. 오리스타틴과 마이탄시노이드와 같은 세포독성 약물을 특징으로 하는 페이로드 분야는 강력한 항종양 활성에 의해 큰 성장 가능성을 지니고 있습니다. 토포이소머라제 억제제와 같은 신흥 페이로드는 새로운 치료 접근법을 제공함으로써 주목을 받고 있습니다. 전략적 제휴 및 R&D 투자는 시장 성장을 가속하고 혁신을 키우고 ADC 파이프라인을 확대하고 있습니다.

시장 세분화
유형 단일클론항체, 링커, 세포독성 물질
제품 애드세트리스, 캐드사이라, 엔허투, 트로델비, 폴리비
서비스 수탁 제조, 위탁 조사, 임상시험 서비스
기술 절단 가능 링커, 비절단성 링커, 부위 특이적 결합
적응증 유방암, 림프종, 백혈병, 폐암, 전립선암, 난소암
최종 사용자 병원, 전문 클리닉, 연구 기관, 제약 회사
프로세스 R&D, 제조, 품질 관리
단계 신약, 전임상, 임상, 상업화
솔루션 맞춤형 항체 개발, 항체 엔지니어링, 링커 개발
투여 경로 정맥내 투여, 피하 투여

시장 현황

항체약물접합체(ADC) 시장에서는 시장 점유율과 가격 전략에 역동적인 변화가 발생하고 있습니다. 각 회사는 혁신적인 가격 모델을 활용하여 접근성 향상과 보급 촉진을 도모하고 있습니다. 신제품의 출시는 매우 중요하며, 제약 대기업은 미충족 요구에 대응하기 위해 최첨단 ADC를 도입하고 있습니다. 이 경쟁 구도는 치료 포트폴리오를 확대하고 시장 존재를 강화하기위한 전략적 제휴 및 파트너십을 특징으로합니다. 맞춤형 의료 및 표적 요법에 대한 관심이 시장 성장을 이끌고 있으며, 첨단 건강 관리 인프라와 활발한 R&D 활동으로 북미가 주도적 지위를 유지하고 있습니다. ADC 시장에서의 경쟁은 치열해지고 있으며, 주요 기업들은 경쟁 우위를 유지하기 위해 연구 개발에 많은 투자를 하고 있습니다. 업계 리더와의 비교 분석을 통해 혁신과 효능에 대한 주력이 분명합니다. 규제의 영향은 크고 ADC의 승인과 상업화는 엄격한 지침에 의해 관리됩니다. 유럽의약청(EMA)과 미국 식품의약국(FDA)은 시장 역학을 형성하는데 중요한 역할을 하고 있습니다. 이러한 규제 준수는 시장 진입과 확대에 필수적입니다. 기술의 진보와 정밀 종양학에 대한 관심 증가로 시장 전망은 유망합니다.

주요 동향과 촉진요인

항체약물접합체(ADC) 시장은 표적암 치료와 맞춤형 의료의 진보에 힘입어 견고한 성장을 이루고 있습니다. 주요 동향으로서 신규 링커와 페이로드의 통합이 진행되어 치료의 유효성과 안전성이 향상되고 있습니다. 제약기업은 연구개발에 대한 투자를 확대하고 ADC 포트폴리오의 혁신과 확충을 도모하고 있습니다. 게다가 세계적으로 암 이환율이 증가하고 있는 것이 보다 효과적인 치료법 수요를 견인하고 있습니다. 규제 당국의 승인과 유리한 상환 정책이 시장 확대를 더욱 촉진하고 있습니다. 세계의 고령화도 암 발생률의 상승에 기여하고 있어 시장 성장을 뒷받침하고 있습니다. 바이오테크놀러지 기업과 학술기관의 연계가 혁신의 속도를 가속화하고 있습니다. 게다가, 비종양 영역에서의 ADC 개발의 동향이 높아지고, 치료 응용의 범위가 넓어지고 있습니다. 헬스케어 인프라가 개선되고 첨단 치료에 대한 인지도가 높아지고 있는 신흥 시장에는 많은 기회가 존재합니다. 본 시장은 지속적인 확대가 전망되고 있습니다.

억제와 도전

항체약물접합체(ADC) 시장은 몇 가지 심각한 제약과 문제에 직면하고 있습니다. 주요 제약은 ADC의 개발 및 제조 비용이 높기 때문에 중소기업 시장 진입을 막을 수 있습니다. 복잡한 제조 공정과 엄격한 규제 요건은 재무 부담을 증가시키고 시장 확대를 제한하고 있습니다. 또 다른 과제는 ADC 기술에 익숙한 숙련 전문가의 부족입니다. 이 인력 부족은 혁신과 개발을 늦추고 시장 성장에 영향을 미칠 수 있습니다. 또한 ADC의 복잡한 특성은 안정성과 안전성에 대한 우려를 초래할 수 있으며, 효능과 환자의 안전성을 보장하기 위해 광범위한 조사와 시험이 필요합니다. 또한 수많은 기업들이 시장 점유율을 겨루는 경쟁 구도이 치열 해지고 가격 압력으로 이어질 수 있습니다. 마지막으로, 개인화된 의료 솔루션과 맞춤형 ADC 요법에 대한 요구는 대량 생산 노력을 복잡하게 하여 물류 및 확장성에 어려움을 낳습니다. 이러한 요인들이 결합되어 ADC 시장의 성장 가능성을 억제하고 있습니다.

목차

제1장 주요 요약

제2장 시장 하이라이트

제3장 시장 역학

  • 거시경제 분석
  • 시장 동향
  • 시장 성장 촉진요인
  • 시장 기회
  • 시장 성장 억제요인
  • CAGR : 성장 분석
  • 영향 분석
  • 신흥 시장
  • 기술 로드맵
  • 전략적 프레임워크

제4장 부문 분석

  • 시장 규모 및 예측 : 유형별
    • 단일클론항체
    • 링커
    • 세포독성물질
  • 시장 규모 및 예측 : 제품별
    • 애드세트리스
    • 캐드사이라
    • 엔허투
    • 트로델비
    • 폴리비
  • 시장 규모 및 예측 : 서비스별
    • 수탁 제조
    • 수탁 조사
    • 임상 시험 서비스
  • 시장 규모 및 예측 : 기술별
    • 절단 가능 링커
    • 비절단성 링커
    • 부위 특이적 결합
  • 시장 규모 및 예측 : 용도별
    • 유방암
    • 림프종
    • 백혈병
    • 폐암
    • 전립선암
    • 난소암
  • 시장 규모 및 예측 : 최종사용자별
    • 병원
    • 전문 클리닉
    • 연구기관
    • 제약기업
  • 시장 규모 및 예측 : 프로세스별
    • 연구개발
    • 제조
    • 품질관리
  • 시장 규모 및 예측 : 개발단계별
    • 신약 개발
    • 전임상 단계
    • 임상
    • 상업화
  • 시장 규모 및 예측 : 솔루션별
    • 맞춤형 항체 개발
    • 항체 공학
    • 링커 개발
  • 시장 규모 및 예측 : 투여 경로별
    • 정맥내 투여
    • 피하 투여

제5장 지역별 분석

  • 북미
    • 미국
    • 캐나다
    • 멕시코
  • 라틴아메리카
    • 브라질
    • 아르헨티나
    • 기타 라틴아메리카
  • 아시아태평양
    • 중국
    • 인도
    • 한국
    • 일본
    • 호주
    • 대만
    • 기타 아시아태평양
  • 유럽
    • 독일
    • 프랑스
    • 영국
    • 스페인
    • 이탈리아
    • 기타 유럽
  • 중동 및 아프리카
    • 사우디아라비아
    • 아랍에미리트(UAE)
    • 남아프리카
    • 사하라 이남 아프리카
    • 기타 중동 및 아프리카

제6장 시장 전략

  • 수요 및 공급 격차 분석
  • 무역 및 물류상의 제약
  • 가격-비용-마진 추세
  • 시장 침투
  • 소비자 분석
  • 규제 개요

제7장 경쟁 정보

  • 시장 포지셔닝
  • 시장 점유율
  • 경쟁 벤치마킹
  • 주요 기업의 전략

제8장 기업 프로파일

  • Seattle Genetics
  • ImmunoGen
  • Mersana Therapeutics
  • ADC Therapeutics
  • Sutro Biopharma
  • Heidelberg Pharma
  • MabPlex International
  • Concortis Biotherapeutics
  • Abzena
  • NBE-Therapeutics
  • Synthon Biopharmaceuticals
  • Alligator Bioscience
  • Zymeworks
  • AstraZeneca Biologics
  • Avid Bioservices

제9장 당사에 대해서

SHW

Antibody Drug Conjugate Market is anticipated to expand from $21 billion in 2024 to $43.9 billion by 2034, growing at a CAGR of approximately 7.7%. The Antibody Drug Conjugate Market encompasses therapeutics that combine monoclonal antibodies with cytotoxic agents, targeting specific cancer cells while minimizing damage to healthy tissues. This market is driven by advancements in targeted cancer therapies, increasing cancer prevalence, and technological innovations in drug delivery systems. The market's growth is further propelled by ongoing clinical trials, regulatory approvals, and strategic collaborations among key industry players.

The Antibody Drug Conjugate (ADC) Market is experiencing robust expansion, driven by advancements in targeted cancer therapies and personalized medicine. The oncology segment is at the forefront, with breast cancer and hematologic malignancies being primary areas of focus due to high unmet needs. Within this segment, breast cancer ADCs are the top performers, offering promising clinical outcomes. Hematologic ADCs follow closely, capitalizing on innovative mechanisms of action. The linker technology segment is pivotal, enhancing ADC stability and efficacy. Cleavable linkers lead in performance, facilitating precise drug release at tumor sites. Non-cleavable linkers also gain traction, offering improved therapeutic indices. The payload segment, featuring cytotoxic agents like auristatins and maytansinoids, shows significant growth potential, driven by their potent anti-tumor activity. Emerging payloads, such as topoisomerase inhibitors, are gaining attention as they offer novel therapeutic avenues. Strategic collaborations and investments in research and development are propelling market growth, fostering innovation and expanding the ADC pipeline.

Market Segmentation
TypeMonoclonal Antibodies, Linkers, Cytotoxins
ProductAdcetris, Kadcyla, Enhertu, Trodelvy, Polivy
ServicesContract Manufacturing, Contract Research, Clinical Trial Services
TechnologyCleavable Linker, Non-cleavable Linker, Site-specific Conjugation
ApplicationBreast Cancer, Lymphoma, Leukemia, Lung Cancer, Prostate Cancer, Ovarian Cancer
End UserHospitals, Specialty Clinics, Research Institutes, Pharmaceutical Companies
ProcessResearch and Development, Manufacturing, Quality Control
StageDiscovery, Preclinical, Clinical, Commercialization
SolutionsCustom Antibody Development, Antibody Engineering, Linker Development
ModeIntravenous, Subcutaneous

Market Snapshot:

The Antibody Drug Conjugate (ADC) market is experiencing dynamic shifts in market share and pricing strategies. Companies are leveraging innovative pricing models to enhance accessibility and drive adoption. New product launches are pivotal, with pharmaceutical giants introducing cutting-edge ADCs to address unmet medical needs. This competitive landscape is characterized by strategic collaborations and partnerships, aiming to expand therapeutic portfolios and enhance market presence. The focus on personalized medicine and targeted therapies is propelling market growth, with North America maintaining a leadership position due to advanced healthcare infrastructure and robust R&D activities. Competition in the ADC market is intensifying, with key players investing heavily in research and development to maintain a competitive edge. Benchmarking against industry leaders reveals a focus on innovation and efficacy. Regulatory influences are significant, as stringent guidelines govern the approval and commercialization of ADCs. The European Medicines Agency and the U.S. FDA play crucial roles in shaping market dynamics. Compliance with these regulations is essential for market entry and expansion. The market's trajectory is promising, driven by technological advancements and an increasing focus on precision oncology.

Geographical Overview:

The Antibody Drug Conjugate (ADC) market is witnessing robust growth across various regions, each with unique dynamics. North America remains dominant, propelled by advanced healthcare infrastructure and substantial investment in biotechnology research. The region's strong pharmaceutical presence and focus on innovation further bolster its market leadership. Europe follows, with significant investments in healthcare research and a supportive regulatory environment fostering a thriving ADC market. The Asia Pacific region is experiencing rapid expansion, driven by increasing healthcare needs and rising investments in biotechnology. Countries like China and India are emerging as key players, with growing pharmaceutical industries and supportive government policies. Latin America and the Middle East & Africa are promising new growth pockets. In Latin America, the market benefits from rising healthcare expenditure and improved access to advanced therapies, while the Middle East & Africa are recognizing the potential of ADCs in addressing unmet medical needs and enhancing treatment outcomes.

Key Trends and Drivers:

The Antibody Drug Conjugate Market is experiencing robust growth, propelled by advances in targeted cancer therapies and personalized medicine. A key trend is the integration of novel linkers and payloads, enhancing the efficacy and safety of these therapies. Pharmaceutical companies are increasingly investing in research and development to innovate and expand their ADC portfolios. Moreover, the growing prevalence of cancer globally is driving demand for more effective treatment options. Regulatory approvals and favorable reimbursement policies are further facilitating market expansion. The aging global population also contributes to the increasing incidence of cancer, thereby boosting market growth. Collaborations between biotech firms and academic institutions are accelerating the pace of innovation. Additionally, there is a rising trend towards the development of ADCs for non-oncological indications, broadening the scope of therapeutic applications. Opportunities abound in emerging markets where healthcare infrastructure is improving, and awareness of advanced therapies is on the rise. This market is poised for sustained expansion.

Restraints and Challenges:

The Antibody Drug Conjugate (ADC) market is confronted with several significant restraints and challenges. A primary restraint is the high cost of ADC development and production, which can deter smaller companies from entering the market. The complex manufacturing processes and stringent regulatory requirements add to the financial burden, limiting market expansion. Another challenge is the limited availability of skilled professionals with expertise in ADC technology. This scarcity can slow innovation and development, impacting market growth. Additionally, the intricate nature of ADCs can lead to stability and safety concerns, requiring extensive research and testing to ensure efficacy and patient safety. Furthermore, the competitive landscape is intensifying, with numerous players vying for market share, which can lead to pricing pressures. Lastly, the need for personalized medicine solutions and tailored ADC therapies complicates mass production efforts, posing logistical and scalability challenges. These factors collectively restrain the ADC market's growth potential.

Key Players:

Seattle Genetics, ImmunoGen, Mersana Therapeutics, ADC Therapeutics, Sutro Biopharma, Heidelberg Pharma, MabPlex International, Concortis Biotherapeutics, Abzena, NBE-Therapeutics, Synthon Biopharmaceuticals, Alligator Bioscience, Zymeworks, AstraZeneca Biologics, Avid Bioservices

Research Scope:

  • Estimates and forecasts the overall market size across type, application, and region.
  • Provides detailed information and key takeaways on qualitative and quantitative trends, dynamics, business framework, competitive landscape, and company profiling.
  • Identifies factors influencing market growth and challenges, opportunities, drivers, and restraints.
  • Identifies factors that could limit company participation in international markets to help calibrate market share expectations and growth rates.
  • Evaluates key development strategies like acquisitions, product launches, mergers, collaborations, business expansions, agreements, partnerships, and R&D activities.
  • Analyzes smaller market segments strategically, focusing on their potential, growth patterns, and impact on the overall market.
  • Outlines the competitive landscape, assessing business and corporate strategies to monitor and dissect competitive advancements.

Our research scope provides comprehensive market data, insights, and analysis across a variety of critical areas. We cover Local Market Analysis, assessing consumer demographics, purchasing behaviors, and market size within specific regions to identify growth opportunities. Our Local Competition Review offers a detailed evaluation of competitors, including their strengths, weaknesses, and market positioning. We also conduct Local Regulatory Reviews to ensure businesses comply with relevant laws and regulations. Industry Analysis provides an in-depth look at market dynamics, key players, and trends. Additionally, we offer Cross-Segmental Analysis to identify synergies between different market segments, as well as Production-Consumption and Demand-Supply Analysis to optimize supply chain efficiency. Our Import-Export Analysis helps businesses navigate global trade environments by evaluating trade flows and policies. These insights empower clients to make informed strategic decisions, mitigate risks, and capitalize on market opportunities.

TABLE OF CONTENTS

1 Executive Summary

  • 1.1 Market Size and Forecast
  • 1.2 Market Overview
  • 1.3 Market Snapshot
  • 1.4 Regional Snapshot
  • 1.5 Strategic Recommendations
  • 1.6 Analyst Notes

2 Market Highlights

  • 2.1 Key Market Highlights by Type
  • 2.2 Key Market Highlights by Product
  • 2.3 Key Market Highlights by Services
  • 2.4 Key Market Highlights by Technology
  • 2.5 Key Market Highlights by Application
  • 2.6 Key Market Highlights by End User
  • 2.7 Key Market Highlights by Process
  • 2.8 Key Market Highlights by Stage
  • 2.9 Key Market Highlights by Solutions
  • 2.10 Key Market Highlights by Mode

3 Market Dynamics

  • 3.1 Macroeconomic Analysis
  • 3.2 Market Trends
  • 3.3 Market Drivers
  • 3.4 Market Opportunities
  • 3.5 Market Restraints
  • 3.6 CAGR Growth Analysis
  • 3.7 Impact Analysis
  • 3.8 Emerging Markets
  • 3.9 Technology Roadmap
  • 3.10 Strategic Frameworks
    • 3.10.1 PORTER's 5 Forces Model
    • 3.10.2 ANSOFF Matrix
    • 3.10.3 4P's Model
    • 3.10.4 PESTEL Analysis

4 Segment Analysis

  • 4.1 Market Size & Forecast by Type (2020-2035)
    • 4.1.1 Monoclonal Antibodies
    • 4.1.2 Linkers
    • 4.1.3 Cytotoxins
  • 4.2 Market Size & Forecast by Product (2020-2035)
    • 4.2.1 Adcetris
    • 4.2.2 Kadcyla
    • 4.2.3 Enhertu
    • 4.2.4 Trodelvy
    • 4.2.5 Polivy
  • 4.3 Market Size & Forecast by Services (2020-2035)
    • 4.3.1 Contract Manufacturing
    • 4.3.2 Contract Research
    • 4.3.3 Clinical Trial Services
  • 4.4 Market Size & Forecast by Technology (2020-2035)
    • 4.4.1 Cleavable Linker
    • 4.4.2 Non-cleavable Linker
    • 4.4.3 Site-specific Conjugation
  • 4.5 Market Size & Forecast by Application (2020-2035)
    • 4.5.1 Breast Cancer
    • 4.5.2 Lymphoma
    • 4.5.3 Leukemia
    • 4.5.4 Lung Cancer
    • 4.5.5 Prostate Cancer
    • 4.5.6 Ovarian Cancer
  • 4.6 Market Size & Forecast by End User (2020-2035)
    • 4.6.1 Hospitals
    • 4.6.2 Specialty Clinics
    • 4.6.3 Research Institutes
    • 4.6.4 Pharmaceutical Companies
  • 4.7 Market Size & Forecast by Process (2020-2035)
    • 4.7.1 Research and Development
    • 4.7.2 Manufacturing
    • 4.7.3 Quality Control
  • 4.8 Market Size & Forecast by Stage (2020-2035)
    • 4.8.1 Discovery
    • 4.8.2 Preclinical
    • 4.8.3 Clinical
    • 4.8.4 Commercialization
  • 4.9 Market Size & Forecast by Solutions (2020-2035)
    • 4.9.1 Custom Antibody Development
    • 4.9.2 Antibody Engineering
    • 4.9.3 Linker Development
  • 4.10 Market Size & Forecast by Mode (2020-2035)
    • 4.10.1 Intravenous
    • 4.10.2 Subcutaneous

5 Regional Analysis

  • 5.1 Global Market Overview
  • 5.2 North America Market Size (2020-2035)
    • 5.2.1 United States
      • 5.2.1.1 Type
      • 5.2.1.2 Product
      • 5.2.1.3 Services
      • 5.2.1.4 Technology
      • 5.2.1.5 Application
      • 5.2.1.6 End User
      • 5.2.1.7 Process
      • 5.2.1.8 Stage
      • 5.2.1.9 Solutions
      • 5.2.1.10 Mode
    • 5.2.2 Canada
      • 5.2.2.1 Type
      • 5.2.2.2 Product
      • 5.2.2.3 Services
      • 5.2.2.4 Technology
      • 5.2.2.5 Application
      • 5.2.2.6 End User
      • 5.2.2.7 Process
      • 5.2.2.8 Stage
      • 5.2.2.9 Solutions
      • 5.2.2.10 Mode
    • 5.2.3 Mexico
      • 5.2.3.1 Type
      • 5.2.3.2 Product
      • 5.2.3.3 Services
      • 5.2.3.4 Technology
      • 5.2.3.5 Application
      • 5.2.3.6 End User
      • 5.2.3.7 Process
      • 5.2.3.8 Stage
      • 5.2.3.9 Solutions
      • 5.2.3.10 Mode
  • 5.3 Latin America Market Size (2020-2035)
    • 5.3.1 Brazil
      • 5.3.1.1 Type
      • 5.3.1.2 Product
      • 5.3.1.3 Services
      • 5.3.1.4 Technology
      • 5.3.1.5 Application
      • 5.3.1.6 End User
      • 5.3.1.7 Process
      • 5.3.1.8 Stage
      • 5.3.1.9 Solutions
      • 5.3.1.10 Mode
    • 5.3.2 Argentina
      • 5.3.2.1 Type
      • 5.3.2.2 Product
      • 5.3.2.3 Services
      • 5.3.2.4 Technology
      • 5.3.2.5 Application
      • 5.3.2.6 End User
      • 5.3.2.7 Process
      • 5.3.2.8 Stage
      • 5.3.2.9 Solutions
      • 5.3.2.10 Mode
    • 5.3.3 Rest of Latin America
      • 5.3.3.1 Type
      • 5.3.3.2 Product
      • 5.3.3.3 Services
      • 5.3.3.4 Technology
      • 5.3.3.5 Application
      • 5.3.3.6 End User
      • 5.3.3.7 Process
      • 5.3.3.8 Stage
      • 5.3.3.9 Solutions
      • 5.3.3.10 Mode
  • 5.4 Asia-Pacific Market Size (2020-2035)
    • 5.4.1 China
      • 5.4.1.1 Type
      • 5.4.1.2 Product
      • 5.4.1.3 Services
      • 5.4.1.4 Technology
      • 5.4.1.5 Application
      • 5.4.1.6 End User
      • 5.4.1.7 Process
      • 5.4.1.8 Stage
      • 5.4.1.9 Solutions
      • 5.4.1.10 Mode
    • 5.4.2 India
      • 5.4.2.1 Type
      • 5.4.2.2 Product
      • 5.4.2.3 Services
      • 5.4.2.4 Technology
      • 5.4.2.5 Application
      • 5.4.2.6 End User
      • 5.4.2.7 Process
      • 5.4.2.8 Stage
      • 5.4.2.9 Solutions
      • 5.4.2.10 Mode
    • 5.4.3 South Korea
      • 5.4.3.1 Type
      • 5.4.3.2 Product
      • 5.4.3.3 Services
      • 5.4.3.4 Technology
      • 5.4.3.5 Application
      • 5.4.3.6 End User
      • 5.4.3.7 Process
      • 5.4.3.8 Stage
      • 5.4.3.9 Solutions
      • 5.4.3.10 Mode
    • 5.4.4 Japan
      • 5.4.4.1 Type
      • 5.4.4.2 Product
      • 5.4.4.3 Services
      • 5.4.4.4 Technology
      • 5.4.4.5 Application
      • 5.4.4.6 End User
      • 5.4.4.7 Process
      • 5.4.4.8 Stage
      • 5.4.4.9 Solutions
      • 5.4.4.10 Mode
    • 5.4.5 Australia
      • 5.4.5.1 Type
      • 5.4.5.2 Product
      • 5.4.5.3 Services
      • 5.4.5.4 Technology
      • 5.4.5.5 Application
      • 5.4.5.6 End User
      • 5.4.5.7 Process
      • 5.4.5.8 Stage
      • 5.4.5.9 Solutions
      • 5.4.5.10 Mode
    • 5.4.6 Taiwan
      • 5.4.6.1 Type
      • 5.4.6.2 Product
      • 5.4.6.3 Services
      • 5.4.6.4 Technology
      • 5.4.6.5 Application
      • 5.4.6.6 End User
      • 5.4.6.7 Process
      • 5.4.6.8 Stage
      • 5.4.6.9 Solutions
      • 5.4.6.10 Mode
    • 5.4.7 Rest of APAC
      • 5.4.7.1 Type
      • 5.4.7.2 Product
      • 5.4.7.3 Services
      • 5.4.7.4 Technology
      • 5.4.7.5 Application
      • 5.4.7.6 End User
      • 5.4.7.7 Process
      • 5.4.7.8 Stage
      • 5.4.7.9 Solutions
      • 5.4.7.10 Mode
  • 5.5 Europe Market Size (2020-2035)
    • 5.5.1 Germany
      • 5.5.1.1 Type
      • 5.5.1.2 Product
      • 5.5.1.3 Services
      • 5.5.1.4 Technology
      • 5.5.1.5 Application
      • 5.5.1.6 End User
      • 5.5.1.7 Process
      • 5.5.1.8 Stage
      • 5.5.1.9 Solutions
      • 5.5.1.10 Mode
    • 5.5.2 France
      • 5.5.2.1 Type
      • 5.5.2.2 Product
      • 5.5.2.3 Services
      • 5.5.2.4 Technology
      • 5.5.2.5 Application
      • 5.5.2.6 End User
      • 5.5.2.7 Process
      • 5.5.2.8 Stage
      • 5.5.2.9 Solutions
      • 5.5.2.10 Mode
    • 5.5.3 United Kingdom
      • 5.5.3.1 Type
      • 5.5.3.2 Product
      • 5.5.3.3 Services
      • 5.5.3.4 Technology
      • 5.5.3.5 Application
      • 5.5.3.6 End User
      • 5.5.3.7 Process
      • 5.5.3.8 Stage
      • 5.5.3.9 Solutions
      • 5.5.3.10 Mode
    • 5.5.4 Spain
      • 5.5.4.1 Type
      • 5.5.4.2 Product
      • 5.5.4.3 Services
      • 5.5.4.4 Technology
      • 5.5.4.5 Application
      • 5.5.4.6 End User
      • 5.5.4.7 Process
      • 5.5.4.8 Stage
      • 5.5.4.9 Solutions
      • 5.5.4.10 Mode
    • 5.5.5 Italy
      • 5.5.5.1 Type
      • 5.5.5.2 Product
      • 5.5.5.3 Services
      • 5.5.5.4 Technology
      • 5.5.5.5 Application
      • 5.5.5.6 End User
      • 5.5.5.7 Process
      • 5.5.5.8 Stage
      • 5.5.5.9 Solutions
      • 5.5.5.10 Mode
    • 5.5.6 Rest of Europe
      • 5.5.6.1 Type
      • 5.5.6.2 Product
      • 5.5.6.3 Services
      • 5.5.6.4 Technology
      • 5.5.6.5 Application
      • 5.5.6.6 End User
      • 5.5.6.7 Process
      • 5.5.6.8 Stage
      • 5.5.6.9 Solutions
      • 5.5.6.10 Mode
  • 5.6 Middle East & Africa Market Size (2020-2035)
    • 5.6.1 Saudi Arabia
      • 5.6.1.1 Type
      • 5.6.1.2 Product
      • 5.6.1.3 Services
      • 5.6.1.4 Technology
      • 5.6.1.5 Application
      • 5.6.1.6 End User
      • 5.6.1.7 Process
      • 5.6.1.8 Stage
      • 5.6.1.9 Solutions
      • 5.6.1.10 Mode
    • 5.6.2 United Arab Emirates
      • 5.6.2.1 Type
      • 5.6.2.2 Product
      • 5.6.2.3 Services
      • 5.6.2.4 Technology
      • 5.6.2.5 Application
      • 5.6.2.6 End User
      • 5.6.2.7 Process
      • 5.6.2.8 Stage
      • 5.6.2.9 Solutions
      • 5.6.2.10 Mode
    • 5.6.3 South Africa
      • 5.6.3.1 Type
      • 5.6.3.2 Product
      • 5.6.3.3 Services
      • 5.6.3.4 Technology
      • 5.6.3.5 Application
      • 5.6.3.6 End User
      • 5.6.3.7 Process
      • 5.6.3.8 Stage
      • 5.6.3.9 Solutions
      • 5.6.3.10 Mode
    • 5.6.4 Sub-Saharan Africa
      • 5.6.4.1 Type
      • 5.6.4.2 Product
      • 5.6.4.3 Services
      • 5.6.4.4 Technology
      • 5.6.4.5 Application
      • 5.6.4.6 End User
      • 5.6.4.7 Process
      • 5.6.4.8 Stage
      • 5.6.4.9 Solutions
      • 5.6.4.10 Mode
    • 5.6.5 Rest of MEA
      • 5.6.5.1 Type
      • 5.6.5.2 Product
      • 5.6.5.3 Services
      • 5.6.5.4 Technology
      • 5.6.5.5 Application
      • 5.6.5.6 End User
      • 5.6.5.7 Process
      • 5.6.5.8 Stage
      • 5.6.5.9 Solutions
      • 5.6.5.10 Mode

6 Market Strategy

  • 6.1 Demand-Supply Gap Analysis
  • 6.2 Trade & Logistics Constraints
  • 6.3 Price-Cost-Margin Trends
  • 6.4 Market Penetration
  • 6.5 Consumer Analysis
  • 6.6 Regulatory Snapshot

7 Competitive Intelligence

  • 7.1 Market Positioning
  • 7.2 Market Share
  • 7.3 Competition Benchmarking
  • 7.4 Top Company Strategies

8 Company Profiles

  • 8.1 Seattle Genetics
    • 8.1.1 Overview
    • 8.1.2 Product Summary
    • 8.1.3 Financial Performance
    • 8.1.4 SWOT Analysis
  • 8.2 ImmunoGen
    • 8.2.1 Overview
    • 8.2.2 Product Summary
    • 8.2.3 Financial Performance
    • 8.2.4 SWOT Analysis
  • 8.3 Mersana Therapeutics
    • 8.3.1 Overview
    • 8.3.2 Product Summary
    • 8.3.3 Financial Performance
    • 8.3.4 SWOT Analysis
  • 8.4 ADC Therapeutics
    • 8.4.1 Overview
    • 8.4.2 Product Summary
    • 8.4.3 Financial Performance
    • 8.4.4 SWOT Analysis
  • 8.5 Sutro Biopharma
    • 8.5.1 Overview
    • 8.5.2 Product Summary
    • 8.5.3 Financial Performance
    • 8.5.4 SWOT Analysis
  • 8.6 Heidelberg Pharma
    • 8.6.1 Overview
    • 8.6.2 Product Summary
    • 8.6.3 Financial Performance
    • 8.6.4 SWOT Analysis
  • 8.7 MabPlex International
    • 8.7.1 Overview
    • 8.7.2 Product Summary
    • 8.7.3 Financial Performance
    • 8.7.4 SWOT Analysis
  • 8.8 Concortis Biotherapeutics
    • 8.8.1 Overview
    • 8.8.2 Product Summary
    • 8.8.3 Financial Performance
    • 8.8.4 SWOT Analysis
  • 8.9 Abzena
    • 8.9.1 Overview
    • 8.9.2 Product Summary
    • 8.9.3 Financial Performance
    • 8.9.4 SWOT Analysis
  • 8.10 NBE-Therapeutics
    • 8.10.1 Overview
    • 8.10.2 Product Summary
    • 8.10.3 Financial Performance
    • 8.10.4 SWOT Analysis
  • 8.11 Synthon Biopharmaceuticals
    • 8.11.1 Overview
    • 8.11.2 Product Summary
    • 8.11.3 Financial Performance
    • 8.11.4 SWOT Analysis
  • 8.12 Alligator Bioscience
    • 8.12.1 Overview
    • 8.12.2 Product Summary
    • 8.12.3 Financial Performance
    • 8.12.4 SWOT Analysis
  • 8.13 Zymeworks
    • 8.13.1 Overview
    • 8.13.2 Product Summary
    • 8.13.3 Financial Performance
    • 8.13.4 SWOT Analysis
  • 8.14 AstraZeneca Biologics
    • 8.14.1 Overview
    • 8.14.2 Product Summary
    • 8.14.3 Financial Performance
    • 8.14.4 SWOT Analysis
  • 8.15 Avid Bioservices
    • 8.15.1 Overview
    • 8.15.2 Product Summary
    • 8.15.3 Financial Performance
    • 8.15.4 SWOT Analysis

9 About Us

  • 9.1 About Us
  • 9.2 Research Methodology
  • 9.3 Research Workflow
  • 9.4 Consulting Services
  • 9.5 Our Clients
  • 9.6 Client Testimonials
  • 9.7 Contact Us
샘플 요청 목록
0 건의 상품을 선택 중
목록 보기
전체삭제