시장보고서
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2094031

표적 단백질 분해(TPD) 시장 : 모달리티, 표적 단백질, 적응증, 개발 단계, 최종 사용자별 - 시장 규모, 업계 역학, 기회 분석 및 예측(2026-2035년)

Global Targeted Protein Degradation Market By Modality, Target Protein, Indication, Development Stage, End User - Market Size, Industry Dynamics, Opportunity Analysis and Forecast For 2026-2035

발행일: | 리서치사: 구분자 Astute Analytica | 페이지 정보: 영문 220 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    



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세계의 표적 단백질 분해(TPD) 시장은 예측 기간 동안 상당한 성장이 예상되며, 2025년 추정 시장 규모인 6억 9,080만 달러에서 2035년까지 약 50억 490만 달러로 확대될 것으로 전망됩니다. 이 시장은 단백질 분해 기술의 급속한 발전, 제약 분야에 대한 투자 확대, 그리고 혁신적인 치료법에 대한 수요 증가에 힘입어 2026년부터 2035년까지 연평균 성장률(CAGR) 21.9%를 나타낼 것으로 예측됩니다.

시장 성장을 주도하는 주요 요인은 차세대 분해 플랫폼, 특히 PROTAC(단백질 분해 표적 키메라) 및 분자 글루의 발전입니다. 이러한 기술은 기존의 억제 기반 접근 방식에서 질병을 유발하는 단백질의 선택적 제거로 전환함으로써 의약품 개발에 새로운 패러다임을 가져왔습니다. 생명공학 기업, 제약사, 연구 기관의 막대한 투자가 시장 발전을 더욱 가속화하고 있습니다. 각 기업은 표적 선택성, 치료 효과 및 안전성 프로파일을 향상시키기 위해 임상 파이프라인 확충, 전략적 제휴 체결, 독자적인 분해 플랫폼 개발을 추진하고 있습니다.

주목할만한 시장 동향

세계의 표적 단백질 분해(TPD) 시장은 혁신적인 분해 플랫폼 개발, 임상 파이프라인 확대, 그리고 종양학, 면역학 및 기타 치료 분야에서 응용을 모색하는 생명공학 기업과 대형 제약사 간의 치열한 경쟁이 특징입니다. Arvinas사는 표적 단백질 분해 분야의 선구자이자 가장 영향력 있는 기업 중 하나로 널리 인정받고 있으며, 업계에서 가장 선진적인 임상 파이프라인 중 하나를 보유하고 있습니다.

카이메라 테라퓨틱스(Chimera Therapeutics)는 단백질 분해 기술의 적용 범위를 기존의 종양학 분야에서 면역학 및 염증성 질환으로 확대함으로써 TPD 시장에서 확고한 입지를 구축하고 있습니다. 브리스톨-마이어스 스퀴브(Bristol-Myers Squibb)는 셀진(Celgene)을 인수하여 중요한 단백질 분해 자산과 전문 지식을 확보함으로써 표적 단백질 분해 분야의 주요 기업로 부상했습니다.

C4 테라퓨틱스는 질환의 원인이 되는 단백질을 제거하도록 설계된 차세대 PROTAC 기술 개발에 주력하고 있습니다. 누릭스 테라퓨틱스는 표적 단백질 분해(TPD) 시장의 또 다른 주요 기업으로, 새로운 이중 기능성 분해제 및 관련 분해 기술 개발을 전문으로 하고 있습니다. 이 회사는 특히 종양학 및 B세포 암과 같은 혈액 악성 종양 분야에서 질환 관련 단백질을 표적으로 하는 치료법 개발에 주력하고 있습니다.

주요 성장 요인

종양학과 정밀 의학은 암 유병률 증가와 치료 내성에 대처할 수 있는 보다 효과적인 치료법에 대한 절실한 수요에 힘입어, 전 세계 표적 단백질 분해(TPD) 시장의 주요 성장 요인으로 자리 잡고 있습니다. 전 세계적으로 악성 질환의 부담이 증가함에 따라, 기존 암 치료의 한계를 극복할 수 있는 혁신적인 치료 접근법에 대한 투자가 가속화되고 있습니다. 표적 단백질 분해는 단순히 질환 관련 단백질의 활성을 억제하는 것이 아니라, 이를 선택적으로 제거하는 근본적으로 다른 작용 기전을 제공하기 때문에 정밀 종양학 분야에서 유망한 전략으로 부상하고 있습니다.

새로운 기회 동향

‘분자 접착제’의 부상은 더 간편하고 효율적이며, 잠재적으로 의약품에 가까운 분해 접근법에 대한 업계의 관심이 높아짐에 힘입어, 전 세계 표적 단백질 분해(TPD) 시장에서 중요한 새로운 기회 동향이 되고 있습니다. PROTAC 및 기타 이중 기능성 분해제는 질환 관련 단백질을 선택적으로 제거하는 능력을 입증함으로써 표적 단백질 분해의 기반을 확립해 왔으나, 분자 접착제는 더 큰 분해제 분자에 수반되는 구조적 및 약동학적 한계를 극복할 수 있는 차세대 치료법으로 주목받고 있습니다. 이들의 독창적인 작용 기전과 단순화된 분자 구조는 치료 표적이 될 수 있는 단백질의 범위를 확대하는 새로운 기회를 창출하고 있습니다.

최적화의 장벽

약동학의 복잡성은 전 세계 표적 단백질 분해(TPD) 시장의 성장을 저해할 수 있는 중대한 과제이며, 특히 PROTAC 및 기타 이중 기능성 분자와 같은 첨단 분해제 모달리티에서 두드러집니다. 이러한 기술들은 선택적 단백질 제거를 통해 획기적인 치료의 가능성을 지니고 있지만, 비교적 복잡한 분자 구조로 인해 기존 저분자 치료제에 비해 의약품 개발에 큰 과제를 안겨주고 있습니다. 분해 유도 분자의 분자 크기 확대, 분자량 증가 및 복잡한 화학적 조성은 용해도, 흡수, 분포, 대사, 배설과 같은 주요 약동학적 특성에 부정적인 영향을 미칠 수 있으며, 그 결과 임상 적용 및 상업적 보급이 제한될 우려가 있습니다.

목차

제1장 주요 요약 : 세계의 표적 단백질 분해(TPD) 시장

제2장 조사 방법 및 프레임워크

제3장 세계의 표적 단백질 분해(TPD) 시장 개요

제4장 세계의 표적 단백질 분해(TPD) 시장 분석

제5장 세계의 표적 단백질 분해(TPD) 시장 분석

제6장 북미 시장 분석

제7장 유럽 시장 분석

제8장 아시아태평양 시장 분석

제9장 중동 및 아프리카 시장 분석

제10장 남미 시장 분석

제11장 기업 개요

제12장 부록

KTH 26.07.27

The global targeted protein degradation (TPD) market is projected to experience substantial growth over the forecast period, expanding from an estimated valuation of USD 690.8 million in 2025 to approximately USD 5,004.9 million by 2035. The market is expected to register a strong compound annual growth rate (CAGR) of 21.9% between 2026 and 2035, driven by rapid advancements in protein degradation technologies, increasing pharmaceutical investment, and growing demand for innovative therapeutic approaches.

A primary factor driving market growth is the advancement of next-generation degradation platforms, particularly PROTACs (proteolysis-targeting chimeras) and molecular glues. These technologies have introduced a new paradigm in pharmaceutical development by shifting from traditional inhibition-based approaches toward selective removal of disease-causing proteins. Significant investment from biotechnology companies, pharmaceutical organizations, and research institutions is further accelerating market development. Companies are expanding clinical pipelines, forming strategic collaborations, and advancing proprietary degradation platforms to improve target selectivity, therapeutic potency, and safety profiles.

Noteworthy Market Developments

The global targeted protein degradation (TPD) market is characterized by strong competition among biotechnology companies and pharmaceutical leaders that are advancing innovative degradation platforms, expanding clinical pipelines, and exploring applications across oncology, immunology, and other therapeutic areas. Arvinas is widely recognized as one of the pioneers and most influential companies in the targeted protein degradation field, with one of the most advanced clinical pipelines in the industry.

Kymera Therapeutics has established a strong position in the TPD market by expanding the application of degradation technologies beyond traditional oncology indications into immunology and inflammatory diseases. Bristol Myers Squibb has become a significant participant in the targeted protein degradation landscape through its acquisition of Celgene, which provided access to important protein degradation assets and expertise.

C4 Therapeutics focuses on advancing next-generation PROTAC technologies designed to eliminate disease-causing proteins. Nurix Therapeutics is another key player in the targeted protein degradation market, specializing in the development of novel bifunctional degraders and related degradation technologies. The company focuses on creating therapies that target disease-associated proteins, particularly within oncology and hematological malignancies such as B-cell cancers.

Core Growth Drivers

Oncology and precision medicine represent major growth drivers for the global targeted protein degradation (TPD) market, supported by the increasing prevalence of cancer and the urgent need for more effective therapies capable of addressing treatment resistance. The growing burden of malignant diseases worldwide has accelerated investment in innovative therapeutic approaches that can overcome the limitations of conventional cancer treatments. Targeted protein degradation has emerged as a promising strategy within precision oncology because it introduces a fundamentally different mechanism of action by selectively eliminating disease-associated proteins rather than simply inhibiting their activity.

Emerging Opportunity Trends

The rise of molecular glues represents a significant emerging opportunity trend within the global targeted protein degradation market, driven by increasing industry interest in simpler, more efficient, and potentially more drug-like degradation approaches. While PROTACs and other bifunctional degraders have established the foundation of targeted protein degradation by demonstrating the ability to selectively eliminate disease-associated proteins, molecular glues are gaining attention as a next-generation modality that may overcome several structural and pharmacokinetic limitations associated with larger degrader molecules. Their unique mechanism and simplified molecular architecture are creating new opportunities for expanding the range of proteins that can be therapeutically targeted.

Barriers to Optimization

Pharmacokinetic complexity represents a significant challenge that may restrain the growth of the global targeted protein degradation market, particularly for advanced degrader modalities such as PROTACs and other bifunctional molecules. Although these technologies offer transformative therapeutic potential through selective protein elimination, their relatively complex molecular structures create substantial drug development challenges compared with conventional small-molecule therapies. The larger molecular size, increased molecular weight, and intricate chemical composition of degrader molecules can negatively influence key pharmacokinetic properties, including solubility, absorption, distribution, metabolism, and elimination, potentially limiting their clinical translation and commercial adoption.

Detailed Market Segmentation

By Modality, PROTACs (proteolysis-targeting chimeras) and bifunctional degraders accounted for the largest share of the global targeted protein degradation market in 2025, driven by their distinctive event-driven pharmacological mechanism and broad therapeutic potential. These advanced degradation platforms have emerged as the leading modality within the targeted protein degradation landscape because they offer a fundamentally different approach from conventional small-molecule therapies. Rather than continuously occupying and blocking the active site of a disease-associated protein, PROTACs are designed to induce selective protein elimination by directing targeted proteins toward the cell's natural degradation machinery. This mechanism enables a more efficient and durable therapeutic response, positioning PROTACs as a transformative technology in precision medicine.

By Target Protein, transcription factors represent one of the fastest-growing and most promising frontiers within the global targeted protein degradation market, driven by the increasing ability of advanced degradation technologies to address previously considered "undruggable" protein targets. Historically, transcription factors have been among the most challenging therapeutic targets due to their lack of well-defined binding pockets and their involvement in complex protein-DNA interactions. Conventional small-molecule inhibitors have often struggled to effectively modulate these proteins because of their large, flat interaction surfaces and dynamic cellular functions. Targeted protein degradation technologies are changing this paradigm by enabling selective elimination of transcription factors rather than attempting to directly inhibit their activity.

By Indication, oncology accounted for the largest share of the global targeted protein degradation market in 2025, maintaining a dominant position due to the significant unmet medical need for innovative cancer therapies capable of addressing treatment resistance and improving patient outcomes. The oncology segment continues to represent the primary focus area for targeted protein degradation research because many cancer-driving proteins have historically been considered difficult or impossible to target using conventional therapeutic approaches. By introducing a fundamentally different mechanism of action, targeted protein degradation technologies offer the potential to eliminate disease-causing proteins rather than merely inhibit their activity, creating new opportunities for treating complex and resistant malignancies.

By Development Stage, the preclinical segment represents the foundational backbone of the global targeted protein degradation market, reflecting an intense phase of scientific innovation, technology refinement, and pipeline expansion. Although clinical-stage candidates attract significant attention due to their potential therapeutic breakthroughs and commercialization prospects, the extensive volume of preclinical research programs ultimately determines the long-term direction and growth potential of the market. The increasing number of early-stage discovery initiatives demonstrates strong confidence among biotechnology companies, pharmaceutical organizations, and academic researchers in the ability of targeted protein degradation technologies to address previously challenging disease targets.

Segment Breakdown

By Modality

  • PROTACs/Bifunctional Degraders
  • Molecular Glues
  • Other [LYTACs, AUTACs]

By Target Protein

  • Transcription Factors
  • Kinases
  • Nuclear Receptors
  • Scaffolding Proteins

By Indication

  • Oncology
  • Immunology & Inflammation
  • Neurodegeneration
  • Others

By Development Stage

  • Preclinical
  • Clinical
  • Approved

By End User

  • Biopharma
  • Academic & Research
  • CROs

By Region

  • North America
  • The U.S.
  • Canada
  • Mexico
  • Europe
  • Western Europe
  • The UK
  • Germany
  • France
  • Italy
  • Spain
  • Rest of Western Europe
  • Eastern Europe
  • Poland
  • Russia
  • Rest of Eastern Europe
  • Asia Pacific
  • China
  • India
  • Japan
  • Australia & New Zealand
  • South Korea
  • ASEAN
  • Rest of Asia Pacific
  • Middle East & Africa (MEA)
  • Saudi Arabia
  • South Africa
  • UAE
  • Rest of MEA
  • South America
  • Argentina
  • Brazil
  • Rest of South America

Geography Breakdown

  • In 2025, North America secured the leading position in the global targeted protein degradation market, supported by substantial venture capital investments, a rapidly expanding biotechnology ecosystem, and a strong pipeline of clinical-stage degradation therapies. The region's dominance is primarily driven by the United States, which serves as the central hub for innovation, research, commercialization, and drug development activities within the targeted protein degradation landscape.
  • The United States contributes more than 75% of North America's targeted protein degradation market revenue, reflecting its strong position in both scientific discovery and commercial translation. Biotechnology companies operating within major innovation hubs benefit from extensive collaborations with leading academic institutions, research organizations, and pharmaceutical partners, enabling rapid advancement of first-in-class protein degradation technologies, including PROTACs (proteolysis-targeting chimeras) and other next-generation targeted degradation approaches.
  • Massachusetts and California remain particularly influential centers for targeted protein degradation innovation due to their dense concentration of biotechnology companies, academic research facilities, and pharmaceutical development capabilities. These ecosystems support continuous innovation by enabling close interaction between basic science researchers, medicinal chemists, computational biologists, and clinical development teams.

Leading Market Participants

  • Bio-Techne
  • Bayer AG
  • BroadPharm
  • BPS Bioscience, Inc.
  • MedChemExpress
  • LifeSensors Inc
  • Promega Corporation
  • Merck KGaA
  • Thermo Fisher Scientific, Inc.
  • Other Prominent Players

Table of Content

Chapter 1. Executive Summary: Global Targeted Protein Degradation Market

Chapter 2. Research Methodology & Research Framework

  • 2.1. Research Objective
  • 2.2. Product Overview
  • 2.3. Market Segmentation
  • 2.4. Qualitative Research
    • 2.4.1. Primary & Secondary Sources
  • 2.5. Quantitative Research
    • 2.5.1. Primary & Secondary Sources
  • 2.6. Breakdown of Primary Research Respondents, By Region
  • 2.7. Assumption for Study
  • 2.8. Market Size Estimation
  • 2.9. Data Triangulation

Chapter 3. Global Targeted Protein Degradation Market Overview

  • 3.1. Industry Value Chain Analysis
    • 3.1.1. E3 Ligase Ligand, Building-Block & Reagent Suppliers
    • 3.1.2. Degrader Discovery Platform & AI-Driven Design Providers
    • 3.1.3. Biopharma Developers & Preclinical / Clinical Programs
    • 3.1.4. CRO, CDMO & Manufacturing Partners
    • 3.1.5. End Users (Biopharma, Academic & Research, CROs)
  • 3.2. Industry Outlook
    • 3.2.1. Overview of the Global Targeted Protein Degradation (TPD) Industry
    • 3.2.2. PROTACs, Molecular Glues & Expansion Beyond Oncology into the 'Undruggable' Proteome
    • 3.2.3. Big-Pharma Licensing Deals, Novel E3 Ligases & AI-Enabled Degrader Discovery
  • 3.3. PESTLE Analysis
  • 3.4. Porter's Five Forces Analysis
    • 3.4.1. Bargaining Power of Suppliers
    • 3.4.2. Bargaining Power of Buyers
    • 3.4.3. Threat of Substitutes
    • 3.4.4. Threat of New Entrants
    • 3.4.5. Degree of Competition
  • 3.5. Market Growth and Outlook
    • 3.5.1. Market Revenue Estimates and Forecast (US$ Mn), 2020-2035
    • 3.5.2. Price Trend Analysis, By Modality

Chapter 4. Global Targeted Protein Degradation Market Analysis

  • 4.1. Competition Dashboard
    • 4.1.1. Market Concentration Rate
    • 4.1.2. Company Market Share Analysis (Value %), 2025
    • 4.1.3. Competitor Mapping & Benchmarking

Chapter 5. Global Targeted Protein Degradation Market Analysis

  • 5.1. Market Dynamics and Trends
    • 5.1.1. Growth Drivers
    • 5.1.2. Restraints
    • 5.1.3. Opportunity
    • 5.1.4. Key Trends
  • 5.2. Market Size and Forecast, 2020-2035 (US$ Mn)
    • 5.2.1. By Modality
      • 5.2.1.1. Key Insights
        • 5.2.1.1.1. PROTACs/Bifunctional Degraders
        • 5.2.1.1.2. Molecular Glues
        • 5.2.1.1.3. Other [LYTACs, AUTACs]
    • 5.2.2. By Target Protein
      • 5.2.2.1. Key Insights
        • 5.2.2.1.1. Transcription Factors
        • 5.2.2.1.2. Kinases
        • 5.2.2.1.3. Nuclear Receptors
        • 5.2.2.1.4. Scaffolding Proteins
    • 5.2.3. By Indication
      • 5.2.3.1. Key Insights
        • 5.2.3.1.1. Oncology
        • 5.2.3.1.2. Immunology & Inflammation
        • 5.2.3.1.3. Neurodegeneration
        • 5.2.3.1.4. Others
    • 5.2.4. By Development Stage
      • 5.2.4.1. Key Insights
        • 5.2.4.1.1. Preclinical
        • 5.2.4.1.2. Clinical
        • 5.2.4.1.3. Approved
    • 5.2.5. By End User
      • 5.2.5.1. Key Insights
        • 5.2.5.1.1. Biopharma
        • 5.2.5.1.2. Academic & Research
        • 5.2.5.1.3. CROs
    • 5.2.6. By Region
      • 5.2.6.1. Key Insights
        • 5.2.6.1.1. North America
          • 5.2.6.1.1.1. The U.S.
          • 5.2.6.1.1.2. Canada
          • 5.2.6.1.1.3. Mexico
        • 5.2.6.1.2. Europe
          • 5.2.6.1.2.1. Western Europe
            • 5.2.6.1.2.1.1. The UK
            • 5.2.6.1.2.1.2. Germany
            • 5.2.6.1.2.1.3. France
            • 5.2.6.1.2.1.4. Italy
            • 5.2.6.1.2.1.5. Spain
            • 5.2.6.1.2.1.6. Rest of Western Europe
          • 5.2.6.1.2.2. Eastern Europe
            • 5.2.6.1.2.2.1. Poland
            • 5.2.6.1.2.2.2. Russia
            • 5.2.6.1.2.2.3. Rest of Eastern Europe
        • 5.2.6.1.3. Asia Pacific
          • 5.2.6.1.3.1. China
          • 5.2.6.1.3.2. India
          • 5.2.6.1.3.3. Japan
          • 5.2.6.1.3.4. Australia & New Zealand
          • 5.2.6.1.3.5. South Korea
          • 5.2.6.1.3.6. ASEAN
          • 5.2.6.1.3.7. Rest of Asia Pacific
        • 5.2.6.1.4. Middle East & Africa (MEA)
          • 5.2.6.1.4.1. Saudi Arabia
          • 5.2.6.1.4.2. South Africa
          • 5.2.6.1.4.3. UAE
          • 5.2.6.1.4.4. Rest of MEA
        • 5.2.6.1.5. South America
          • 5.2.6.1.5.1. Argentina
          • 5.2.6.1.5.2. Brazil
          • 5.2.6.1.5.3. Rest of South America

Chapter 6. North America Market Analysis

  • 6.1. Market Dynamics and Trends
    • 6.1.1. Growth Drivers
    • 6.1.2. Restraints
    • 6.1.3. Opportunity
    • 6.1.4. Key Trends
  • 6.2. Market Size and Forecast, 2020-2035 (US$ Mn)
    • 6.2.1. Key Insights
      • 6.2.1.1. By Modality
      • 6.2.1.2. By Target Protein
      • 6.2.1.3. By Indication
      • 6.2.1.4. By Development Stage
      • 6.2.1.5. By End User
      • 6.2.1.6. By Country

Chapter 7. Europe Market Analysis

  • 7.1. Market Dynamics and Trends
    • 7.1.1. Growth Drivers
    • 7.1.2. Restraints
    • 7.1.3. Opportunity
    • 7.1.4. Key Trends
  • 7.2. Market Size and Forecast, 2020-2035 (US$ Mn)
    • 7.2.1. Key Insights
      • 7.2.1.1. By Modality
      • 7.2.1.2. By Target Protein
      • 7.2.1.3. By Indication
      • 7.2.1.4. By Development Stage
      • 7.2.1.5. By End User
      • 7.2.1.6. By Country

Chapter 8. Asia Pacific Market Analysis

  • 8.1. Market Dynamics and Trends
    • 8.1.1. Growth Drivers
    • 8.1.2. Restraints
    • 8.1.3. Opportunity
    • 8.1.4. Key Trends
  • 8.2. Market Size and Forecast, 2020-2035 (US$ Mn)
    • 8.2.1. Key Insights
      • 8.2.1.1. By Modality
      • 8.2.1.2. By Target Protein
      • 8.2.1.3. By Indication
      • 8.2.1.4. By Development Stage
      • 8.2.1.5. By End User
      • 8.2.1.6. By Country

Chapter 9. Middle East & Africa Market Analysis

  • 9.1. Market Dynamics and Trends
    • 9.1.1. Growth Drivers
    • 9.1.2. Restraints
    • 9.1.3. Opportunity
    • 9.1.4. Key Trends
  • 9.2. Market Size and Forecast, 2020-2035 (US$ Mn)
    • 9.2.1. Key Insights
      • 9.2.1.1. By Modality
      • 9.2.1.2. By Target Protein
      • 9.2.1.3. By Indication
      • 9.2.1.4. By Development Stage
      • 9.2.1.5. By End User
      • 9.2.1.6. By Country

Chapter 10. South America Market Analysis

  • 10.1. Market Dynamics and Trends
    • 10.1.1. Growth Drivers
    • 10.1.2. Restraints
    • 10.1.3. Opportunity
    • 10.1.4. Key Trends
  • 10.2. Market Size and Forecast, 2020-2035 (US$ Mn)
    • 10.2.1. Key Insights
      • 10.2.1.1. By Modality
      • 10.2.1.2. By Target Protein
      • 10.2.1.3. By Indication
      • 10.2.1.4. By Development Stage
      • 10.2.1.5. By End User
      • 10.2.1.6. By Country

Chapter 11. Company Profile (Company Overview, Financial Matrix, Key Product landscape, Key Personnel, Key Competitors, Contact Address, and Business Strategy Outlook)

  • 11.1. Bio-Techne
  • 11.2. Bayer AG
  • 11.3. BroadPharm
  • 11.4. BPS Bioscience, Inc.
  • 11.5. MedChemExpress
  • 11.6. LifeSensors Inc
  • 11.7. Promega Corporation
  • 11.8. Merck KGaA
  • 11.9. Thermo Fisher Scientific, Inc.
  • 11.10. Other Prominent Players

Chapter 12. Annexure

  • 12.1. List of Secondary Sources
  • 12.2. Key Country Markets- Macro Economic Outlook/Indicators
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