시장보고서
상품코드
1984875

엑소좀 요법 시장 : 엑소좀 유래별, 치료법별, 치료 환경별, 치료 사용 사례별, 투여 방법별, 규제 분류별, 지역별 - 시장 규모, 업계 역학, 기회 분석, 예측(2026-2035년)

Global Exosome Therapy Market: By Exosome Source Type, Treatment Setting, Therapeutic Use Case, Administration Approach, Regulatory Classification, Region - Market Size, Industry Dynamics, Opportunity Analysis and Forecast for 2026-2035

발행일: | 리서치사: 구분자 Astute Analytica | 페이지 정보: 영문 320 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    



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

엑소좀 치료제 시장은 큰 변화의 한가운데에 있으며, 과거에는 투기적이고 틈새 시장이었던 분야가 이제는 큰 경제적 가치를 지닌 급성장 산업으로 진화하고 있습니다. 현재 581억 달러 규모인 이 시장은 향후 수년간 괄목할 만한 성장을 이룰 것으로 예상되며, 2035년까지 3,096억 달러를 넘어설 것으로 예측됩니다. 2026-2035년 기간 중 18.20%의 연평균 복합 성장률(CAGR)을 보일 것으로 예측되며, 이는 투자자들의 신뢰가 높아지고 엑솜을 이용한 치료법이 널리 보급되고 있다는 것을 보여줍니다.

이 시장의 진화를 이끄는 주요 요인 중 하나는 기존의 살아있는 줄기세포를 이용한 치료에서 '세포가 없는' 엑소좀 제품으로의 전환입니다. 이러한 전환은 줄기세포 치료와 관련된 문제, 특히 안전성과 확장성에 대한 우려를 해결하고자 하는 요구에 의해 촉발되었습니다. 세포에서 분비되는 작은 세포외 소포인 엑소좀은 세포 자체에 기인하는 위험 없이 줄기세포의 치료 효과의 대부분을 유지한다는 점에서 유망한 대안으로 떠오르고 있습니다.

주목할 만한 시장 동향

이 산업은 치열한 경쟁과 전통 있는 바이오제약 기업, 전문 바이오테크놀러지 기업, 연구 툴 프로바이더 등 다양한 기업이 존재하는 것이 특징입니다. 이러한 조합은 혁신과 전략적 움직임이 성공에 필수적인 역동적인 상황을 만들어 냈습니다. 각 유형의 기업은 첨단 연구 능력에서 전문 기술 플랫폼에 이르기까지 시장에 고유한 강점을 가져와 풍부하고 다면적인 경쟁 환경을 형성하고 있습니다.

이 분야의 진전을 촉진하는 주요 기업으로는 Coya Therapeutics, Evox Therapeutics, Curexsys, EV Therapeutics, SHIFTBIO, Capricor Therapeutics, Aethlon Medical 등을 들 수 있습니다. 이들 기업은 독자적인 기술력뿐만 아니라 다양한 전략적 노력을 통해 시장에서의 입지를 강화하기 위해 적극적으로 움직이고 있습니다.

이들 기업은 파트너십을 구축하는 것 외에도 GMP(Good Manufacturing Practice) 기준에 부합하는 확장 가능한 생산 기술 개발에 많은 투자를 하고 있습니다. 이러한 노력은 제조 공정이 엄격한 규제 요건을 충족할 수 있도록 보장하며, 바이오의약품의 안전하고 일관된 생산에 필수적인 요소입니다.

주요 성장 촉진요인

세계에서 증가하는 암 발병률은 엑소좀을 이용한 면역치료 및 표적 약물전달시스템에 대한 수요를 견인하는 중요한 요인입니다. 전 세계에서 암 발병률이 지속적으로 증가하고 있는 가운데, 부작용을 최소화하면서 환자의 예후를 개선할 수 있는 보다 효과적이고 정밀한 치료법 개발이 시급한 실정입니다. 엑소좀을 이용한 치료법은 면역체계를 조절하고, 높은 특이성을 가지고 치료제를 종양세포에 직접 전달할 수 있는 능력을 가지고 있으므로 이러한 상황에서 큰 주목을 받고 있습니다.

새로운 기회의 동향

엑소좀 치료 시장에서 가장 수익성이 높은 기회는 재생 치료 영역을 넘어 약물전달 분야에 존재합니다. 재생치료는 손상된 조직을 복구하고 치유하는 능력으로 큰 주목을 받고 있지만, 고효율 약물전달 매체로서의 엑소좀의 가능성은 더 큰 상업적 잠재력을 지닌 혁신적인 새로운 영역으로 떠오르고 있습니다. 이 기회는 주로 지질 나노입자(LNP)와 바이러스 벡터에 의존하는 세계 바이오의약품 시장에서 현재 약물전달 시스템의 한계에 의해 주도되고 있습니다. 이러한 기술들은 상당한 성공을 거두었지만, 독성을 유발하거나 면역반응을 유발하는 등 심각한 단점을 동반하는 경우가 많습니다.

최적화 장벽

엑소좀 치료제 시장의 성장은 업계 전반의 표준화 및 품질관리 부족으로 인해 심각한 문제에 직면해 있습니다. 현재 엑소좀의 분리, 특성화, 제조에 대한 보편적으로 받아들여지는 프로토콜은 존재하지 않으며, 그 결과 엑소좀 치료제의 제조 방법은 매우 다양합니다. 이러한 표준화된 절차의 부재는 로트 간 편차가 20%를 초과하는 경우가 많으며, 이는 엑소좀 제품의 구성과 품질이 생산 로트마다 크게 달라질 수 있다는 것을 의미합니다. 이러한 불균일성은 치료 결과의 신뢰성과 예측 가능성을 저해하며, 이는 임상의, 환자, 규제 당국의 신뢰를 얻는 데 매우 중요한 요소입니다.

목차

제1장 개요 : 세계의 엑소좀 요법 시장

제2장 조사 방법 및 조사 프레임워크

제3장 세계의 엑소좀 요법 시장 개요

제4장 세계의 엑소좀 요법 시장 분석

제5장 세계의 엑소좀 요법 시장 분석

제6장 북미의 시장 분석

제7장 유럽의 시장 분석

제8장 아시아태평양의 시장 분석

제9장 중동 및 아프리카의 시장 분석

제10장 남미의 시장 분석

제11장 기업 개요

제12장 부록

KSA 26.04.16

The exosome therapy market is undergoing a significant transformation, evolving from a speculative and niche segment into a rapidly expanding industry with substantial economic value. Currently valued at USD 58.1 billion, the market is projected to experience impressive growth over the coming years, with forecasts estimating it will exceed USD 309.6 billion by 2035. This remarkable expansion reflects a compound annual growth rate (CAGR) of 18.20% during the period from 2026 to 2035, highlighting both increasing investor confidence and growing adoption of exosome-based therapies.

One of the key factors driving this market evolution is the shift from traditional live stem cell therapies toward "cell-free" exosome products. This transition is motivated by the desire to address some of the challenges associated with stem cell treatments, particularly concerns related to safety and scalability. Exosomes, which are small extracellular vesicles secreted by cells, offer a promising alternative because they carry many of the therapeutic benefits of stem cells without the risks linked to the cells themselves.

Noteworthy Market Developments

The industry is characterized by intense competition and a diverse array of players, including well-established biopharmaceutical companies, specialized biotechnology firms, and providers of research tools. This blend creates a dynamic landscape where innovation and strategic maneuvering are essential for success. Each type of company brings unique strengths to the market, from advanced research capabilities to specialized technology platforms, contributing to a rich and multifaceted competitive environment.

Among the key participants driving progress in this sector are companies such as Coya Therapeutics, Evox Therapeutics, Curexsys, EV Therapeutics, SHIFTBIO, Capricor Therapeutics, and Aethlon Medical. These organizations are not only advancing their proprietary technologies but also actively seeking to strengthen their market positions through various strategic initiatives.

In addition to forging alliances, these companies are heavily investing in the development of scalable production technologies that comply with Good Manufacturing Practice (GMP) standards. This focus ensures that their manufacturing processes meet stringent regulatory requirements, which is crucial for the safe and consistent production of biopharmaceutical products.

Core Growth Drivers

The increasing global incidence of cancer is a significant factor driving the demand for exosome-based immunotherapy and targeted drug delivery systems. As cancer rates continue to rise worldwide, there is an urgent need for more effective and precise treatment options that can improve patient outcomes while minimizing side effects. Exosome-based therapies have garnered considerable attention in this context because of their ability to modulate the immune system and deliver therapeutic agents directly to tumor cells with high specificity.

Emerging Opportunity Trends

The most lucrative opportunity within the exosome therapy market extends beyond regenerative treatments and lies in the domain of drug delivery. While regenerative therapies have garnered significant attention for their ability to repair and heal damaged tissues, the potential of exosomes as highly efficient drug delivery vehicles is emerging as a transformative frontier with even greater commercial promise. This opportunity is driven by the limitations of current drug delivery systems in the global biologics market, which predominantly depend on Lipid Nanoparticles (LNPs) and viral vectors. Although these technologies have achieved considerable success, they are often accompanied by significant drawbacks, such as triggering toxicity or provoking immune responses.

Barriers to Optimization

The growth of the exosome therapy market faces significant challenges due to the lack of standardization and quality control across the industry. Currently, there are no universally accepted protocols for the isolation, characterization, and manufacturing of exosomes, which creates considerable variability in how these therapies are produced. This absence of standardized procedures results in high batch-to-batch variability, often exceeding 20%, meaning that the composition and quality of exosome products can differ substantially from one production run to another. Such inconsistencies undermine the reliability and predictability of therapeutic outcomes, which are critical factors for gaining the trust of clinicians, patients, and regulators alike.

Detailed Market Segmentation

By treatment setting, the hospital-based therapies segment emerged as the largest treatment setting within the exosome therapy market, capturing a significant market share of 39%. This leadership position is largely attributed to the nature of the conditions treated and the complexity involved in administering certain exosome therapies. Many of these therapies, particularly those designed for acute and severe conditions such as Acute Respiratory Distress Syndrome (ARDS), require careful and continuous inpatient monitoring to ensure patient safety and optimal therapeutic outcomes.

By therapeutic use case, the regenerative therapies segment holds a commanding position within the exosome therapy market, securing a leading market share of 52% in 2025. This dominance is largely driven by the clinical validation of exosomes' remarkable ability to accelerate tissue repair, especially in the treatment of chronic wounds. Unlike traditional cell-based grafts, which often involve complex procedures and carry risks such as immune rejection or limited integration, exosome therapies offer a more efficient and less invasive alternative.

By exosome source type, the stem cell-derived exosomes segment stood out by securing the largest market share, commanding an impressive 62% in 2025. This dominant position reflects the unique biological advantages that stem cell-derived exosomes offer compared to other sources. Among stem cells, Mesenchymal Stem Cells (MSCs) have emerged as the preferred "bio-factories" within the industry. MSCs are especially valued because their exosomes are naturally enriched with a diverse array of bioactive lipids and proteins that play critical roles in tissue repair and regeneration.

By therapy modality, the autologous exosome therapy category emerged as the clear leader, capturing the largest market share of 57% in 2025. This dominance is firmly grounded in scientific rationale, as autologous therapies utilize exosomes derived directly from the patient's own cells. This approach offers superior biocompatibility, significantly minimizing the risk of immune rejection that can occur with allogeneic therapies, which use exosomes sourced from donors. Because the exosomes are patient-specific, they are more readily accepted by the body's immune system, enhancing both safety and therapeutic efficacy.

Segment Breakdown

By Therapy Modality

  • Autologous Exosome Therapy
  • Patient-derived cell exosomes
  • Point-of-care or near-patient processing
  • Allogeneic Exosome Therapy
  • Donor-derived standardized exosomes
  • Off-the-shelf exosome preparations

By Treatment Setting

  • Hospital-based therapies
  • Specialty clinics
  • Orthopedic clinics
  • Neurology clinics
  • Oncology clinics
  • Ambulatory surgical centers
  • Wellness/aesthetic centers

By Therapeutic Use Case

  • Regenerative therapies
  • Musculoskeletal repair
  • Wound healing
  • Anti-inflammatory therapies
  • Neurorestorative therapies
  • Cardiometabolic therapies
  • Aesthetic & cosmetic therapies
  • Skin rejuvenation
  • Hair restoration
  • Supportive/adjunctive therapies

By Administration Approach

  • Systemic therapy
  • IV-based exosome therapy
  • Local therapy
  • Intra-articular
  • Intradermal
  • Intrathecal
  • Topical application

By Exosome Source Type

  • Stem cell-derived exosomes
  • Immune cell-derived exosomes
  • Tissue-derived exosomes
  • Plant-derived exosomes

By Regulatory Classification

  • Regulated therapeutic procedures
  • Compassionate-use / experimental therapies
  • Non-regulated / wellness-based therapies

By Region

  • North America
  • Europe
  • Asia Pacific
  • Middle East and Africa
  • South America

Geography Breakdown

  • North America is not only leading the global exosome therapy market but is also setting the standards that other regions are beginning to follow. In 2025, the region commands a substantial 46.80% share of the market, highlighting its pivotal role in shaping the future of exosome therapies worldwide. This dominance is largely attributed to the region's regulatory environment, which embraces a "high-risk, high-reward" approach. This framework encourages innovation by allowing promising therapies to advance rapidly through clinical development while providing clear pathways for regulatory approval.
  • A major milestone that catalyzed North America's leadership was the historic filing on January 2, 2025, of the first Biologics License Application (BLA) by Capricor Therapeutics. This event was a watershed moment because it effectively positioned the U.S. Food and Drug Administration (FDA) as the global gatekeeper for exosome therapy approvals. The FDA's clear regulatory stance provided much-needed clarity and legitimacy to the field, alleviating uncertainties that had previously slowed investment and development. As a result, venture capitalists gained increased confidence in the market's potential, leading to a surge in funding.

Leading Market Participants

  • Aethlon Medical Inc.
  • Bluebird Bio Inc.
  • Capricor Therapeutics Inc.
  • Codiak BioSciences Inc.
  • EV Therapeutics
  • Evox Therapeutics Ltd.
  • Exosome Sciences Inc.
  • Invivo Therapeutics Holdings Corp.
  • Kintor Pharmaceutical Limited
  • MBR Therapeutics
  • Medivir AB
  • NanoString Technologies Inc.
  • ReNeuron Group plc
  • Sorrento Therapeutics Inc.
  • System Biosciences LLC
  • Other Prominent Players

Table of Content

Chapter 1. Executive Summary: Global Exosome Therapy 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 Exosome Therapy Market Overview

  • 3.1. Industry Value Chain Analysis
    • 3.1.1. Raw Material & Biological Source Providers
    • 3.1.2. Exosome Isolation & Manufacturing Technology Providers
    • 3.1.3. Contract Development & Manufacturing Organizations (CDMOs)
    • 3.1.4. Therapy Developers & Biotechnology Companies
    • 3.1.5. Healthcare Providers & Clinical Institutions
  • 3.2. Industry Outlook
    • 3.2.1. Clinical Development Landscape
    • 3.2.2. Regulatory Landscape
    • 3.2.3. Disease Burden & Therapeutic Potential
  • 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

Chapter 4. Global Exosome Therapy 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 Exosome Therapy 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 Therapy Modality
      • 5.2.1.1. Key Insights
        • 5.2.1.1.1. Autologous Exosome Therapy
          • 5.2.1.1.1.1. Patient-derived cell exosomes
          • 5.2.1.1.1.2. Point-of-care or near-patient processing
        • 5.2.1.1.2. Allogeneic Exosome Therapy
          • 5.2.1.1.2.1. Donor-derived standardized exosomes
          • 5.2.1.1.2.2. Off-the-shelf exosome preparations
    • 5.2.2. By Treatment Setting
      • 5.2.2.1. Key Insights
        • 5.2.2.1.1. Hospital-based therapies
        • 5.2.2.1.2. Specialty clinics
          • 5.2.2.1.2.1. Orthopedic clinics
          • 5.2.2.1.2.2. Neurology clinics
          • 5.2.2.1.2.3. Oncology clinics
        • 5.2.2.1.3. Ambulatory surgical centers
        • 5.2.2.1.4. Wellness/aesthetic centers
    • 5.2.3. By Administration Approach
      • 5.2.3.1. Key Insights
        • 5.2.3.1.1. Systemic Administration
          • 5.2.3.1.1.1. Intravenous (IV)
        • 5.2.3.1.2. Localized Administration
          • 5.2.3.1.2.1. Intra-articular
          • 5.2.3.1.2.2. Intradermal
          • 5.2.3.1.2.3. Intrathecal
          • 5.2.3.1.2.4. Topical application
    • 5.2.4. By Exosome Source Type
      • 5.2.4.1. Key Insights
        • 5.2.4.1.1. Stem cell-derived exosomes
        • 5.2.4.1.2. Immune cell-derived exosomes
        • 5.2.4.1.3. Tissue-derived exosomes
        • 5.2.4.1.4. Plant-derived exosomes
    • 5.2.5. By Regulatory Classification
      • 5.2.5.1. Key Insights
        • 5.2.5.1.1. Regulated therapeutic procedures
        • 5.2.5.1.2. Compassionate-use / experimental therapies
        • 5.2.5.1.3. Non-regulated / wellness-based therapies
    • 5.2.6. By Therapeutic Use Case
      • 5.2.6.1. Key Insights
        • 5.2.6.1.1. Regenerative therapies
          • 5.2.6.1.1.1. Musculoskeletal repair
          • 5.2.6.1.1.2. Wound healing
        • 5.2.6.1.2. Anti-inflammatory therapies
        • 5.2.6.1.3. Neurorestorative therapies
        • 5.2.6.1.4. Cardiometabolic therapies
        • 5.2.6.1.5. Aesthetic & cosmetic therapies
          • 5.2.6.1.5.1. Skin rejuvenation
          • 5.2.6.1.5.2. Hair restoration
        • 5.2.6.1.6. Supportive/adjunctive therapies
    • 5.2.7. By Region
      • 5.2.7.1. Key Insights
        • 5.2.7.1.1. North America
          • 5.2.7.1.1.1. The U.S.
          • 5.2.7.1.1.2. Canada
          • 5.2.7.1.1.3. Mexico
        • 5.2.7.1.2. Europe
          • 5.2.7.1.2.1. Western Europe
            • 5.2.7.1.2.1.1. The UK
            • 5.2.7.1.2.1.2. Germany
            • 5.2.7.1.2.1.3. France
            • 5.2.7.1.2.1.4. Italy
            • 5.2.7.1.2.1.5. Spain
            • 5.2.7.1.2.1.6. Rest of Western Europe
          • 5.2.7.1.2.2. Eastern Europe
            • 5.2.7.1.2.2.1. Poland
            • 5.2.7.1.2.2.2. Russia
            • 5.2.7.1.2.2.3. Rest of Eastern Europe
        • 5.2.7.1.3. Asia Pacific
          • 5.2.7.1.3.1. China
          • 5.2.7.1.3.2. India
          • 5.2.7.1.3.3. Japan
          • 5.2.7.1.3.4. South Korea
          • 5.2.7.1.3.5. Australia & New Zealand
          • 5.2.7.1.3.6. ASEAN
            • 5.2.7.1.3.6.1. Indonesia
            • 5.2.7.1.3.6.2. Malaysia
            • 5.2.7.1.3.6.3. Thailand
            • 5.2.7.1.3.6.4. Singapore
            • 5.2.7.1.3.6.5. Rest of ASEAN
          • 5.2.7.1.3.7. Rest of Asia Pacific
        • 5.2.7.1.4. Middle East & Africa
          • 5.2.7.1.4.1. UAE
          • 5.2.7.1.4.2. Saudi Arabia
          • 5.2.7.1.4.3. South Africa
          • 5.2.7.1.4.4. Rest of MEA
        • 5.2.7.1.5. South America
          • 5.2.7.1.5.1. Argentina
          • 5.2.7.1.5.2. Brazil
          • 5.2.7.1.5.3. 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 Therapy Modality
      • 6.2.1.2. By Treatment Setting
      • 6.2.1.3. By Administration Approach
      • 6.2.1.4. By Exosome Source Type
      • 6.2.1.5. By Regulatory Classification
      • 6.2.1.6. By Therapeutic Use Case
      • 6.2.1.7. 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 Therapy Modality
      • 7.2.1.2. By Treatment Setting
      • 7.2.1.3. By Administration Approach
      • 7.2.1.4. By Exosome Source Type
      • 7.2.1.5. By Regulatory Classification
      • 7.2.1.6. By Therapeutic Use Case
      • 7.2.1.7. 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 Therapy Modality
      • 8.2.1.2. By Treatment Setting
      • 8.2.1.3. By Administration Approach
      • 8.2.1.4. By Exosome Source Type
      • 8.2.1.5. By Regulatory Classification
      • 8.2.1.6. By Therapeutic Use Case
      • 8.2.1.7. 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 Therapy Modality
      • 9.2.1.2. By Treatment Setting
      • 9.2.1.3. By Administration Approach
      • 9.2.1.4. By Exosome Source Type
      • 9.2.1.5. By Regulatory Classification
      • 9.2.1.6. By Therapeutic Use Case
      • 9.2.1.7. 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 Therapy Modality
      • 10.2.1.2. By Treatment Setting
      • 10.2.1.3. By Administration Approach
      • 10.2.1.4. By Exosome Source Type
      • 10.2.1.5. By Regulatory Classification
      • 10.2.1.6. By Therapeutic Use Case
      • 10.2.1.7. 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. Aethlon Medical Inc.
  • 11.2. Capricor Therapeutics Inc.
  • 11.3. Codiak BioSciences
  • 11.4. EV Therapeutics
  • 11.5. Evox Therapeutics Ltd.
  • 11.6. Exosome Sciences Inc.
  • 11.7. ReNeuron Group plc
  • 11.8. System Biosciences LLC
  • 11.9. Aruna Bio, Inc.
  • 11.10. NurExone Biologic
  • 11.11. Aegle Therapeutics
  • 11.12. 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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