시장보고서
상품코드
2126356

BRAF 동반진단 시장 : 전략적 인사이트 및 예측(2026-2035년)

BRAF Companion Diagnostics Market - Strategic Insights and Forecasts (2026-2035)

발행일: | 리서치사: 구분자 Knowledge Sourcing Intelligence | 페이지 정보: 영문 180 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    



가격
PDF & Excel (Single User License) help
PDF, Excel 보고서를 1명만 이용할 수 있는 라이선스입니다. 텍스트 등의 복사 및 붙여넣기는 가능하지만, 출처를 명시해야 합니다. 인쇄는 1회만 가능하며, 인쇄물의 이용 범위는 PDF 및 Excel 파일의 이용 범위에 따릅니다.
US $ 3,950 금액 안내 화살표 ₩ 5,388,000
PDF & Excel (Multi User License - Up to 5 Users) help
PDF, Excel 보고서를 동일 사업장에서 5명까지 이용할 수 있는 라이선스입니다. 텍스트 등의 복사 및 붙여넣기는 가능하지만, 출처를 명시해야 합니다. 인쇄는 5회까지만 가능하며, 인쇄물의 이용은 PDF 및 Excel 파일의 이용 범위에 따릅니다.
US $ 4,550 금액 안내 화살표 ₩ 6,206,000
PDF & Excel (Enterprise License) help
PDF, Excel 보고서를 동일 기업의 모든 분이 이용할 수 있는 라이선스입니다. 텍스트 등의 복사 및 붙여넣기는 가능하지만, 출처를 명시해야 합니다. 인쇄 횟수에는 제한이 없으며, 인쇄된 문서의 이용 범위는 PDF 및 Excel 파일의 이용 범위에 따릅니다.
US $ 6,950 금액 안내 화살표 ₩ 9,480,000
※ 부가세 별도
한글목차
영문목차
※ 본 상품은 영문 자료로 한글과 영문 목차에 불일치하는 내용이 있을 경우 영문을 우선합니다. 정확한 검토를 위해 영문 목차를 참고해주시기 바랍니다.

BRAF 동반진단 시장은 2026년 11억 달러에서 2035년에는 27억 6,000만 달러로 확대되고, CAGR 10.8%를 나타낼 것으로 예측됩니다.

BRAF 동반진단 시장은 정밀 종양학으로의 패러다임 전환과 BRAF 표적 치료의 활용 확대에 힘입어 큰 변화를 겪고 있습니다. 이 시장의 진화는 흑색종, 대장암, 비소세포폐암, 갑상선암 등 여러 암 유형에 걸친 치료 방침 결정에 있어 BRAF 돌연변이의 정확한 확인이 필수적이라는 인식이 높아지고 있다는 점이 특징입니다. 중합효소 연쇄반응(PCR), 차세대 염기서열 분석, 체액 생검 등 첨단 분자 기술의 융합으로 BRAF 돌연변이 검출은 더욱 신속하고 종합적으로 이루어지며, 접근성도 점점 더 용이해지고 있습니다. 표적 치료의 선택지가 계속 확대되는 가운데, 의료 시스템에서는 유전체 검사가 일상적인 종양학 워크플로우에 통합되어 있으며, 이로 인해 검증된 동반진단 솔루션에 대한 지속적인 수요가 발생하고 있습니다. 정밀의료 전략의 임상적 가치가 입증됨에 따라 제약사들은 바이오마커 주도 신약 개발에 대한 투자를 강화하고 있으며, 새로운 치료법과 진단법을 연계할 필요성이 커지고 있습니다. 치료 성과는 신뢰할 수 있는 바이오마커의 확인에 달려 있기 때문에 규제 당국은 동반진단의 검증에 계속해서 중점을 두고 있습니다. 시장에서는 종합적인 유전체 프로파일링, 체액 생검 기술, AI 기반 분석 도구에 대한 막대한 투자가 이루어지고 있으며, BRAF 동반진단은 전 세계 의료 시스템에서 정밀 종양학의 핵심 구성 요소로서 입지를 확고히 다져가고 있습니다.

시장 성장 촉진요인

  • 정밀 종양학의 확산은 BRAF 동반진단 시장의 주요 촉진요인으로 작용하고 있습니다. 치료 결과가 실용적인 바이오마커의 식별에 점점 더 의존하게 됨에 따라, 정밀 종양학은 분자 수준의 특성 평가에 기반을 두고 있습니다. 표적 치료의 선택지가 지속적으로 확대됨에 따라, 의료 제공업체들은 유전체 검사를 일상적인 종양학 워크플로우에 통합하고 있습니다. 기존의 치료 접근 방식은 개인화가 제한적인 경우가 많아, 동반진단의 추가적인 활용을 요구하는 압력이 높아지고 있습니다. 진단 개발 기업들은 바이오마커의 식별과 임상적 유용성을 향상시키는 분자 검사 플랫폼 개발을 추진하고 있습니다. 이러한 동향은 BRAF 동반진단에 대한 수요를 강화시키고 있으며, 그 결과 BRAF 동반진단의 활용이 지속적으로 확대되고 있습니다. 표적 치료제 개발이 진행됨에 따라 동반진단에 대한 수요가 증가하고 있으며, 시장 확대가 더욱 가속화되고 있습니다. 표적 치료는 바이오마커 상태에 따라 치료 효과가 달라지기 때문에 정확한 돌연변이 검출에 의존하고 있습니다. 정밀의료 전략이 임상적 가치를 입증함에 따라, 제약 기업들은 바이오마커 주도 신약 개발에 대한 투자를 확대되고 있습니다. 치료 포트폴리오가 확충됨에 따라, 환자 선정을 지원하는 검증된 동반진단에 대한 수요가 증가하고 있습니다. 각 진단 장비 제조업체들은 신흥 치료법과 검사 솔루션을 연계하기 위해 제약 개발 기업들과의 협력을 강화하고 있습니다. 이러한 협력이 시장의 지속적인 성장을 뒷받침하고 있습니다. 종합적인 유전체 프로파일링의 활용 확대가 보다 광범위한 분자 평가의 도입을 촉진하고 있습니다. 종합적인 유전체 프로파일링을 통해 여러 치료 표적 변이를 동시에 식별할 수 있으므로 치료 방침 결정이 용이해집니다. 암 치료 경로가 더욱 복잡해짐에 따라 수요는 보다 광범위한 분자 평가로 전환되고 있습니다. 순차적 검사 방식에서는 진단 지연이나 업무 부담이 증가하는 경우가 많습니다. 검사 기관에서는 검사 효율과 진단 수율을 향상시키는 첨단 시퀀싱 기술을 도입하고 있습니다. 이러한 동향은 동반진단 솔루션의 활용을 더욱 촉진하고 있습니다. 질환의 경과에 따른 모니터링에 대한 수요가 증가함에 따라, BRAF 동반진단의 임상적 중요성이 확대되고 있습니다. 종양의 생물학적 특성은 시간이 지남에 따라 변화하므로, 질환의 진행이나 치료 저항성은 치료 효과에 영향을 미칩니다. 의료진은 치료 과정 전반에 걸쳐 분자 수준의 변화를 모니터링하려는 경향이 강해지고 있습니다. 단일 시점의 검사만으로는 장기적인 질환 관리에 필요한 정보가 불충분한 경우가 적지 않습니다. 진단 장비 제조업체들은 반복적인 분자 평가 및 내성 모니터링을 지원하는 기술을 개발하고 있습니다.

시장 제약 요인

  • 고도의 분자 검사에 수반되는 높은 비용은 보험 적용 범위가 제한적인 의료 시스템에서 도입을 저해할 가능성이 있습니다. 첨단 기술에 필요한 막대한 자금 투자는 소규모 의료 기관이나 개발도상 지역에게 장벽이 됩니다. 유전체 검사 인프라에 대한 접근성이 고르지 않은 것은 신흥 의료 시장에서 동반진단의 이용 가능성을 저하시킬 수 있습니다. 전문 검사실 및 훈련된 인력의 부족은 분자진단의 확장성을 제한하고 있습니다. 규제상의 검증 요건은 개발의 복잡성을 가중시켜 진단 제조업체의 상품화까지 소요되는 기간을 연장시킵니다. 엄격한 증거 요건은 개발자에게 막대한 시간적·비용적 부담을 안겨줍니다. 서로 다른 관할 구역에 걸친 규제의 복잡성은 새로운 진단 솔루션의 상용화를 목표로 하는 제조업체에게 규정 준수상의 부담이 되고 있습니다.

목차

제1장 주요 요약

제2장 조사 방법

제3장 BRAF 동반진단 시장 : 개요, 시장 규모와 예측

제4장 시장 역학

제5장 업계 상황

제6장 혁신 동향

제7장 규제 상황

제8장 BRAF 동반진단 시장 : 전망 분석

제9장 BRAF 동반진단 시장 : 부문 분석

제10장 BRAF 동반진단 시장 : 지역별 분석

제11장 BRAF 동반진단 시장 : 국가별 분석

제12장 경쟁 구도

제13장 기업 개요

제14장 BRAF 동반진단 시장 : 상업 예측 분석

제15장 투자 및 자금조달 분석

제16장 향후 전망

JHS 26.09.17

The BRAF Companion Diagnostics Market is anticipated to grow at a CAGR of 10.8% from USD 1.10 billion in 2026 to USD 2.76 billion in 2035.

The BRAF companion diagnostics market is undergoing significant transformation driven by the paradigm shift toward precision oncology and the expanding availability of BRAF-targeted therapies. The market's evolution is characterized by the growing recognition that accurate identification of BRAF mutations is essential for therapeutic decision-making across multiple cancer types, including melanoma, colorectal cancer, non-small cell lung cancer, and thyroid cancer. The convergence of advanced molecular technologies, including polymerase chain reaction, next-generation sequencing, and liquid biopsy, is enabling faster, more comprehensive, and increasingly accessible BRAF mutation detection. Healthcare systems are incorporating genomic testing into routine oncology workflows as targeted treatment options continue expanding, creating sustained demand for validated companion diagnostic solutions. Pharmaceutical companies are strengthening investments in biomarker-driven drug development as precision medicine strategies demonstrate clinical value, increasing the need for diagnostic alignment with emerging therapies. Regulatory agencies continue emphasizing companion diagnostic validation because treatment outcomes depend on reliable biomarker identification. The market is witnessing significant investment in comprehensive genomic profiling, liquid biopsy technologies, and AI-enabled interpretation tools, positioning BRAF companion diagnostics as a critical component of precision oncology across global healthcare systems.

Market Drivers

  • The expanding adoption of precision oncology represents the primary driver for the BRAF companion diagnostics market. Precision oncology relies on molecular characterization because treatment outcomes increasingly depend on identification of actionable biomarkers. Healthcare providers are incorporating genomic testing into routine oncology workflows as targeted treatment options continue expanding. Conventional treatment approaches often provide limited personalization, creating pressure for greater use of companion diagnostics. Diagnostic developers are advancing molecular testing platforms that improve biomarker identification and clinical utility. This trend strengthens demand for BRAF companion diagnostics, resulting in sustained growth in BRAF companion diagnostic utilization. The growth of targeted therapeutic development is further accelerating market expansion through increased demand for companion diagnostics. Targeted therapies depend on accurate mutation detection because therapeutic effectiveness varies according to biomarker status. Pharmaceutical companies are expanding investments in biomarker-driven drug development as precision medicine strategies demonstrate clinical value. Broader therapeutic portfolios increase demand for validated companion diagnostics that support patient selection. Diagnostic manufacturers are strengthening collaborations with pharmaceutical developers to align testing solutions with emerging therapies. This integration supports continued market growth. The increasing utilization of comprehensive genomic profiling is driving adoption of broader molecular assessment. Comprehensive genomic profiling enhances treatment decision-making because multiple actionable mutations can be identified simultaneously. Demand is shifting toward broader molecular assessment as oncology treatment pathways become more complex. Sequential testing approaches often increase diagnostic delays and operational burden. Laboratories are adopting advanced sequencing technologies that improve testing efficiency and diagnostic yield. These developments support greater utilization of companion diagnostic solutions. Rising demand for longitudinal disease monitoring is expanding the clinical relevance of BRAF companion diagnostics. Disease progression and treatment resistance influence therapeutic effectiveness because tumor biology evolves over time. Healthcare providers are increasingly monitoring molecular changes throughout treatment pathways. Single-timepoint testing often provides insufficient information for long-term disease management. Diagnostic companies are developing technologies that support repeat molecular assessment and resistance monitoring.

Market Restraints

  • High costs associated with advanced molecular testing can limit adoption across healthcare systems with restricted reimbursement coverage. The significant financial investment required for advanced technologies creates barriers for smaller facilities and developing regions. Uneven access to genomic testing infrastructure can reduce availability of companion diagnostics in emerging healthcare markets. The shortage of specialized laboratories and trained personnel limits the scalability of molecular diagnostics. Regulatory validation requirements increase development complexity and extend commercialization timelines for diagnostic manufacturers. The rigorous evidence requirements create significant time and cost burdens for developers. Regulatory complexities across different jurisdictions create compliance burdens for manufacturers seeking to commercialize new diagnostic solutions.

Technology and Segment Insights

  • The technology landscape is characterized by the growing importance of comprehensive genomic profiling and integrated molecular testing platforms. PCR-based testing maintains a strong position because it provides rapid and highly sensitive detection of clinically actionable mutations. Growing utilization of targeted therapies is increasing demand for fast turnaround times because treatment decisions often depend on timely biomarker confirmation. NGS is expanding comprehensive biomarker assessment and enabling simultaneous evaluation of multiple mutations. Sanger sequencing remains important for confirmation and research applications. IHC continues supporting protein expression assessment where applicable. Liquid biopsy is increasing testing accessibility through minimally invasive sampling. The segment analysis reveals that melanoma represents the largest application area because BRAF mutations occur frequently within this patient population and directly influence treatment selection. Expanding use of targeted therapies is increasing demand for mutation testing because clinicians require accurate biomarker identification before initiating treatment. BRAF V600E represents the most widely tested mutation type because it remains the primary predictive biomarker for approved targeted therapies. Colorectal cancer, NSCLC, and thyroid cancer represent significant and growing segments with expanding therapeutic options. Tissue biopsy remains the clinical reference standard for BRAF mutation detection. Liquid biopsy is expanding for minimally invasive testing when tissue samples are limited, supporting longitudinal disease monitoring. Clinical diagnostic laboratories represent the leading end-user segment, with hospitals and specialty cancer centers expanding testing capabilities. The integration of AI is becoming increasingly important because large-scale genomic datasets create interpretation challenges. Technology developers are integrating AI into genomic workflows to improve analytical performance.

Competitive and Strategic Outlook

  • The competitive landscape features established diagnostics and life science companies alongside specialized precision oncology and liquid biopsy providers. Roche remains strategically distinct because it combines targeted oncology therapeutics with companion diagnostic development under an integrated precision medicine framework, expanding integrated diagnostic solutions that support molecular profiling across multiple tumor types. QIAGEN differentiates itself through molecular testing expertise and extensive experience in companion diagnostic partnerships, enhancing molecular diagnostics platforms and bioinformatics support capabilities to address evolving clinical requirements. Thermo Fisher Scientific benefits from a broad portfolio spanning molecular diagnostics, sequencing technologies, and oncology-focused testing solutions, expanding NGS and oncology testing capabilities to support precision medicine implementation. Agilent maintains a strong position through its expertise in pathology, molecular diagnostics, and biomarker testing technologies, enhancing diagnostic workflows and pathology solutions that support molecular testing efficiency. Illumina occupies a strategic position because sequencing technologies increasingly support comprehensive molecular profiling in oncology, strengthening oncology-focused sequencing solutions to support precision medicine adoption. Abbott differentiates itself through established diagnostic infrastructure and global commercial reach, investing in molecular diagnostics capabilities that support personalized treatment approaches. Bio-Rad maintains competitive strength through advanced molecular testing technologies and mutation detection expertise, expanding digital PCR and molecular testing capabilities. Companies are pursuing product portfolio expansion through innovation in NGS panels, liquid biopsy assays, and AI-enabled interpretation tools. Strategic collaborations between diagnostic manufacturers and pharmaceutical companies are increasing, driven by the need for companion diagnostic development alongside targeted therapies. Geographic expansion remains a key strategic priority, with companies targeting rapidly growing Asia Pacific and emerging markets where healthcare infrastructure is expanding.

Short Conclusion

  • The BRAF companion diagnostics market is positioned for sustained growth driven by the convergence of precision oncology, targeted therapeutic development, and technological innovation. The transition from single-gene testing toward comprehensive genomic profiling represents a fundamental shift in precision oncology. While challenges related to high costs, infrastructure limitations, and regulatory complexity persist, strategic investments in technology, partnerships, and evidence generation are creating durable competitive advantages for market leaders. The long-term market outlook remains positive, with BRAF companion diagnostics evolving into a critical component of precision oncology, supporting accurate patient stratification, treatment optimization, and improved clinical outcomes across global healthcare systems.

Key Benefits of this Report

  • Insightful Analysis: Detailed market insights across regions, customer segments, policies, socio-economic factors, consumer preferences, and industry verticals.
  • Competitive Landscape: Understand strategic moves by key players to identify optimal market entry approaches.
  • Market Drivers and Future Trends: Assess major growth forces and emerging developments shaping the market.
  • Actionable Recommendations: Support strategic decisions to unlock new revenue streams.
  • Caters to a Wide Audience: Suitable for startups, research institutions, consultants, SMEs, and large enterprises.

What Businesses Use Our Reports For

  • Industry and market insights, opportunity assessment, product demand forecasting, market entry strategy, geographical expansion, capital investment decisions, regulatory analysis, new product development, and competitive intelligence.

Report Coverage

  • Historical data from 2021 to 2024, Base year 2025, and Forecast years from 2026 to 2035
  • Growth opportunities, challenges, supply chain outlook, regulatory framework, and trend analysis
  • Competitive positioning, strategies, and market share evaluation, and trade analysis
  • Revenue growth and forecast assessment across segments and regions
  • Company profiling including strategies, products, financials, and key developments

TABLE OF CONTENTS

1. Executive Summary

  • 1.1 Market Snapshot
  • 1.2 Key Findings
  • 1.3 Analyst Insights
  • 1.4 Strategic Recommendations

2. Research Methodology

  • 2.1 Research Design
  • 2.2 Data Collection Methodology
  • 2.3 Market Size Estimation
  • 2.4 Forecasting Model
  • 2.5 Assumptions & Limitations

3. BRAF Companion Diagnostics Market Overview, Size & Forecast

  • 3.1 Market Definition & Scope
  • 3.2 BRAF-Mutated Cancer Overview
  • 3.3 Industry Evolution
  • 3.4 Key Market Trends
  • 3.5 Historical Market Size Analysis (2021-2025)
  • 3.6 Market Forecast Analysis (2026-2035)
  • 3.7 Disease Burden and Unmet Clinical Needs Analysis
  • 3.8 Epidemiology and Prevalence Analysis of BRAF-Mutated Cancers
  • 3.9 Diagnosed Patient Population Analysis
  • 3.10 BRAF Testing Volume Analysis
  • 3.11 Precision Oncology Adoption Analysis
  • 3.12 Treatment Landscape and Companion Diagnostic Integration

4. Market Dynamics

  • 4.1 Market Drivers
  • 4.2 Market Restraints
  • 4.3 Market Opportunities
  • 4.4 Market Challenges

5. Industry Landscape

  • 5.1 Industry Value Chain Analysis
  • 5.2 Pricing Analysis
  • 5.3 Reimbursement Landscape

6. Innovation Landscape

  • 6.1 Emerging Technologies in BRAF Testing
  • 6.2 Product Innovation Trends
  • 6.3 Clinical Trial Analysis
  • 6.4 Pipeline Analysis of BRAF Companion Diagnostics
  • 6.5 Next-Generation Sequencing Integration
  • 6.6 Liquid Biopsy Applications in BRAF Mutation Detection
  • 6.7 AI Integration in Molecular Diagnostics
  • 6.8 Technology Roadmap

7. Regulatory Landscape

  • 7.1 Regulatory Framework
  • 7.2 Approval Pathways
  • 7.3 Compliance Requirements

8. BRAF Companion Diagnostics Market Landscape Analysis

  • 8.1 Analysis by Technology Platform
  • 8.2 Analysis by BRAF Mutation Type
  • 8.3 Analysis by Sample Type
  • 8.4 Analysis by Clinical Application
  • 8.5 Analysis by Testing Methodology
  • 8.6 Analysis by Cancer Indication

9. BRAF Companion Diagnostics Market Segment Analysis (2021-2035)

  • 9.1 By Technology
    • 9.1.1 Polymerase Chain Reaction (PCR)
    • 9.1.2 Next-Generation Sequencing (NGS)
    • 9.1.3 Sanger Sequencing
    • 9.1.4 Immunohistochemistry (IHC)
    • 9.1.5 Other Technologies
  • 9.2 By Cancer Indication
    • 9.2.1 Melanoma
    • 9.2.2 Colorectal Cancer
    • 9.2.3 Non-Small Cell Lung Cancer (NSCLC)
    • 9.2.4 Thyroid Cancer
    • 9.2.5 Other Solid Tumors
  • 9.3 By Mutation Type
    • 9.3.1 BRAF V600E
    • 9.3.2 BRAF V600K
    • 9.3.3 BRAF V600R
    • 9.3.4 Non-V600 BRAF Mutations
    • 9.3.5 Other BRAF Mutations
  • 9.4 By Sample Type
    • 9.4.1 Tissue Biopsy
    • 9.4.2 Liquid Biopsy
  • 9.5 By End User
    • 9.5.1 Hospitals
    • 9.5.2 Clinical Diagnostic Laboratories
    • 9.5.3 Academic and Research Institutes
    • 9.5.4 Specialty Cancer Centers

10. BRAF Companion Diagnostics Market Geographical Analysis (2021-2035)

  • 10.1 North America
  • 10.2 Europe
  • 10.3 Asia-Pacific
  • 10.4 South America
  • 10.5 Middle East & Africa

11. BRAF Companion Diagnostics Market Country Analysis (2021-2035)

  • 11.1 United States
  • 11.2 Canada
  • 11.3 Germany
  • 11.4 United Kingdom
  • 11.5 France
  • 11.6 Italy
  • 11.7 Spain
  • 11.8 Japan
  • 11.9 China
  • 11.10 South Korea
  • 11.11 Australia
  • 11.12 India
  • 11.13 Brazil
  • 11.14 Saudi Arabia

12. Competitive Landscape

  • 12.1 Market Share Analysis
  • 12.2 Strategic Developments
  • 12.3 Mergers & Acquisitions, Partnerships & Collaborations
  • 12.4 Product Launches

13. Company Profiles

  • 13.1 F. Hoffmann-La Roche Ltd.
    • 13.1.1 Company Overview
    • 13.1.2 Financials
    • 13.1.3 Product Portfolio
    • 13.1.4 Recent Developments
  • 13.2 QIAGEN N.V.
  • 13.3 Thermo Fisher Scientific Inc.
  • 13.4 Agilent Technologies, Inc.
  • 13.5 Illumina, Inc.
  • 13.6 Bio-Rad Laboratories, Inc.
  • 13.7 Guardant Health, Inc.
  • 13.8 Foundation Medicine, Inc.
  • 13.9 NeoGenomics Laboratories, Inc.
  • 13.10 Danaher Corporation
  • 13.11 Sysmex Corporation
  • 13.12 Myriad Genetics, Inc.
  • 13.13 Leica Biosystems Nussloch GmbH
  • 13.14 Personalis, Inc.
  • 13.15 Exact Sciences Corporation

14. BRAF Companion Diagnostics Market Commercial Forecast Analysis

  • 14.1 BRAF V600E Companion Diagnostic Solutions
  • 14.2 PCR-Based BRAF Testing Solutions
  • 14.3 NGS-Based BRAF Testing Solutions
  • 14.4 Liquid Biopsy-Based BRAF Testing Solutions
  • 14.5 Melanoma Companion Diagnostic Solutions
  • 14.6 Colorectal Cancer Companion Diagnostic Solutions
  • 14.7 Comprehensive Genomic Profiling Platforms

15. Investment & Funding Analysis

  • 15.1 Venture Capital Trends
  • 15.2 Government Funding
  • 15.3 R&D Investments

16. Future Outlook

  • 16.1 Key Growth Opportunities
  • 16.2 Future Industry Trends
샘플 요청 목록
0 건의 상품을 선택 중
목록 보기
전체삭제
문의
원하시는 정보를
찾아 드릴까요?
문의주시면 필요한 정보를
신속하게 찾아드릴게요.
02-2025-2992
email
문의하기