市场调查报告书
商品编码
1466286
伴同性诊断市场:按技术、适应症和最终用户划分 - 2024-2030 年全球预测Companion Diagnostics Market by Technology (Immunohistochemistry, In Situ Hybridization, Next-Generation Sequencing), Indication (Cancer, Cardiovascular Diseases, Infectious Diseases), End-user - Global Forecast 2024-2030 |
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伴同性诊断市场规模预计2023年为66.4亿美元,2024年达73亿美元,预计2030年将达到134.9亿美元,复合年增长率为10.65%。
伴同性诊断是专门的测试,旨在帮助医疗保健专业人员确定特定的医疗程序对患者是否有效,并确定该个体的最佳剂量。这些测试是个人化医疗的重要组成部分,个人化医疗是一种根据每个患者的个人特征(包括生活方式、遗传倾向和环境)提供量身定制治疗的医疗方法。伴同性诊断被广泛使用,特别是在某些癌症的治疗中,其中治疗效果可能会受到肿瘤内存在的遗传改变的极大影响。个人化医疗的发展,即根据患者个别情况优化治疗,是伴同性诊断需求的主要驱动力。此外,标靶治疗的开发,特别是在肿瘤学领域,需要伴同性诊断来识别将从这些治疗中受益最多的患者。然而,开发和引入伴同性诊断的成本高昂,报销不足是一个主要障碍。此外,次世代定序和数位 PCR 等技术正在扩展伴同性诊断的能力,并实现更全面的基因分析,为市场成长提供了巨大的机会。
主要市场统计 | |
---|---|
基准年[2023] | 66.4亿美元 |
预测年份 [2024] | 73亿美元 |
预测年份 [2030] | 134.9亿美元 |
复合年增长率(%) | 10.65% |
科技 精准医疗领域对次世代定序仪的偏好日益增加
免疫组织化学 (IHC) 是一种透过检测组织切片中细胞中的蛋白质来诊断疾病的技术。它广泛用于癌症诊断,以识别有助于确定癌症类型及其对治疗的潜在反应的特异性标记。当诊断重点是组织样本中蛋白质表现的定位和定性评估时,首选 IHC。原位杂交 (ISH) 能够检测和定位组织切片或细胞样本中的特定 DNA 或 RNA 序列,从而深入了解基因表现和染色体畸变。该技术在检测与某些癌症相关的特定基因重排和扩增方面特别有用。次世代定序仪(NGS) 透过以前所未有的速度和规模对整个基因组或感兴趣区域进行定序,提供对基因组成的全面洞察。 NGS 是需要广泛了解遗传变异(包括小突变、拷贝数变异等)的应用的首选技术,这些变异可能与多种疾病的标靶治疗选择相关。聚合酵素链锁反应(PCR) 是一种用于增强 DNA 或 RNA 小片段以促进进一步分析的技术。 PCR 由于其简单性、敏感性和特异性而成为最广泛使用的技术之一。 PCR 因其快速处理时间而备受青睐,使其成为需要快速决策以选择治疗方法的疾病的理想选择。
最终用户製药和生物製药领域的扩展推动了伴同性诊断的重要性
製药和生物製药公司主要从事治疗药物的发现、开发和商业化。伴同性诊断的整合在标靶治疗治疗的开发过程中至关重要,特别是在癌症治疗中。这些公司需要伴同性诊断来监测治疗反应并根据需要调整治疗计划。参考文献实验室是执行复杂且先进的诊断测试的专业设施,而标准医院实验室通常无法提供这些测试。它们透过提供复杂的测试来帮助识别与特定疾病和治疗反应相关的生物标记物,在实施伴同性诊断中发挥重要作用。
区域洞察
在美洲,强大的医疗基础设施、日益增强的个人化医疗意识以及重要的研发活动推动了对伴同性诊断的需求。美国食品药物管理局(FDA) 在核准癌症治疗伴同性诊断方面特别积极,并强调了这些工具在治疗决策中的重要性。该地区的投资和倡议主要集中在癌症、心血管疾病和神经病学领域,反映出个人化医疗解决方案的更广泛趋势。欧盟国家对伴同性诊断表现出很高的需求,并得到强有力的法律规范促进创新,同时确保病人安全。欧洲药品管理局 (EMA) 在整个欧洲核准伴同性诊断方面发挥关键作用。欧盟消费者的需求复杂,对个人化医疗服务抱有很高的期望。在阿拉伯联合大公国和沙乌地阿拉伯等中东国家,在政府措施和医疗基础设施投资的支持下,人们对个人化医疗的兴趣与日俱增。然而,由于卫生基础设施和服务有限,非洲面临重大障碍。在亚太地区,在政府旨在普及医疗保健标准和促进个人化医疗的倡议的推动下,伴同性诊断市场正在迅速扩大。政府推出了多项推动精准医疗的倡议,包括对基因研究的大量投资。这种关注逐渐体现在对伴同性诊断不断增长的需求上,尤其是在设备齐全的都市区。
FPNV定位矩阵
FPNV 定位矩阵对于评估伴同性诊断市场至关重要。我们检视与业务策略和产品满意度相关的关键指标,以对供应商进行全面评估。这种深入的分析使用户能够根据自己的要求做出明智的决策。根据评估,供应商被分为四个成功程度不同的像限:前沿(F)、探路者(P)、利基(N)和重要(V)。
市场占有率分析
市场占有率分析是一种综合工具,可以对伴同性诊断市场中供应商的现状进行富有洞察力和深入的研究。全面比较和分析供应商在整体收益、基本客群和其他关键指标方面的贡献,以便更好地了解公司的绩效及其在争夺市场占有率时面临的挑战。此外,该分析还提供了对该行业竞争特征的宝贵见解,包括在研究基准年观察到的累积、分散主导地位和合併特征等因素。详细程度的提高使供应商能够做出更明智的决策并制定有效的策略,从而在市场上获得竞争优势。
1. 市场渗透率:提供有关主要企业所服务的市场的全面资讯。
2. 市场开拓:我们深入研究利润丰厚的新兴市场,并分析其在成熟细分市场的渗透率。
3. 市场多元化:提供有关新产品发布、开拓地区、最新发展和投资的详细资讯。
4.竞争评估与资讯:对主要企业的市场占有率、策略、产品、认证、监管状况、专利状况、製造能力等进行全面评估。
5. 产品开发与创新:提供对未来技术、研发活动和突破性产品开发的见解。
1.伴同性诊断市场的市场规模和预测是多少?
2.在伴同性诊断市场的预测期间内,有哪些产品、细分市场、应用和领域需要考虑投资?
3.伴同性诊断市场的技术趋势和法规结构是什么?
4.伴同性诊断市场主要厂商的市场占有率为何?
5.进入伴同性诊断市场的合适型态和策略手段是什么?
[194 Pages Report] The Companion Diagnostics Market size was estimated at USD 6.64 billion in 2023 and expected to reach USD 7.30 billion in 2024, at a CAGR 10.65% to reach USD 13.49 billion by 2030.
Companion diagnostics are specialized tests designed to help healthcare professionals determine whether a particular medical treatment is effective for a patient or to identify the best dosage of medication for that individual. These tests are an integral part of personalized medicine, a medical approach that tailors treatment to the individual characteristics of each patient, such as their lifestyle, genetic makeup, and environment. Companion diagnostics are particularly prevalent in the management of certain cancers, where the effectiveness of the treatment can depend significantly on the genetic alterations present within the tumor. The push towards personalized medicine, where treatments are optimized for individual patient profiles, significantly drives the demand for companion diagnostics. Moreover, the development of targeted therapies, especially in oncology, necessitates companion diagnostics to identify patients who would most benefit from these treatments. However, the development and implementation of companion diagnostics can be costly, with inadequate reimbursement posing a significant barrier. Furthermore, technologies, including next-generation sequencing and digital PCR, are expanding the capabilities of companion diagnostics, allowing for more comprehensive genetic profiling poses significant opportunities for market growth.
KEY MARKET STATISTICS | |
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Base Year [2023] | USD 6.64 billion |
Estimated Year [2024] | USD 7.30 billion |
Forecast Year [2030] | USD 13.49 billion |
CAGR (%) | 10.65% |
Technology: Increasing preference of next-generation sequencing in precision medicine
Immunohistochemistry (IHC) is a technique used to diagnose diseases by detecting proteins in tissue section cells. It is widely employed in cancer diagnostics to identify specific markers that help in determining the type of cancer and its potential responsiveness to treatments. IHC is preferred when the diagnostic focus is on the localization and qualitative assessment of protein expressions in tissue samples. Situ Hybridization (ISH) permits the detection and localization of specific DNA or RNA sequences in tissue sections or cell samples, providing insights into gene expression and chromosomal abnormalities. This technology is particularly valuable in detecting specific gene rearrangements or amplifications associated with certain cancers. Next-generation sequencing (NGS) offers comprehensive insights into the genetic makeup by allowing the sequencing of entire genomes or targeted regions of interest at an unprecedented speed and scale. NGS is the technology of choice for applications requiring a broad understanding of genetic variations, including small mutations, copy number variations, and others that may be relevant for selecting targeted therapies across various diseases. Polymerase Chain Reaction (PCR) is a technique utilized to strengthen small segments of DNA or RNA, making it easier to conduct further analyses. It stands as one of the most widely used technologies due to its simplicity, sensitivity, and specificity. PCR is highly favored for its rapid turnaround times, making it ideal for diseases requiring quick decision-making for therapy selection.
End-user: Expansion of pharmaceutical and biopharmaceutical sector driving the significance of companion diagnostics
Pharmaceutical and biopharmaceutical companies engaged primarily in the discovery, development, and commercialization of therapeutics. The integration of companion diagnostics is crucial in the drug development process, especially for targeted therapies, including those used in cancer treatment. These companies need companion diagnostics to monitor responses to therapy and adjust treatment plans as necessary. Reference laboratories are specialized facilities that perform complex and advanced diagnostic testing, often not available in standard hospital labs. They play a critical role in the implementation of companion diagnostics by providing high-complexity tests that help in the identification of biomarkers associated with specific diseases and treatment responses.
Regional Insights
In the Americas, the demand for companion diagnostics is driven by a robust healthcare infrastructure, heightened awareness about personalized medicine, and significant research and development activities. The U.S. Food and Drug Administration (FDA) has been proactive in approving companion diagnostics, especially for cancer treatments, which underscores the importance of these tools in therapeutic decisions. Investments and initiatives in this region are primarily focused on oncology, cardiovascular diseases, and neurology, reflecting a broader trend toward personalized healthcare solutions. EU countries exhibit a high demand for companion diagnostics, supported by a strong regulatory framework that promotes innovation while ensuring patient safety. The European Medicines Agency (EMA) plays an vital role in the approval of companion diagnostics across Europe. Consumer needs in the EU are sophisticated, with a high expectation for personalized healthcare services. Middle Eastern countries, such as the United Arab Emirates and Saudi Arabia, are witnessing a growing interest in personalized medicine, which is supported by government initiatives and investments in healthcare infrastructure. Africa, however, faces significant hurdles due to limited healthcare infrastructure and access. In APAC, the market for companion diagnostics is expanding swiftly, fueled by government initiatives aimed at improving healthcare standards and embracing personalized medicine. The government has launched several initiatives to promote precision medicine, including significant investments in genetic research. This focus is gradually translating into increased demand for companion diagnostics, particularly in urban areas with better healthcare facilities.
FPNV Positioning Matrix
The FPNV Positioning Matrix is pivotal in evaluating the Companion Diagnostics Market. It offers a comprehensive assessment of vendors, examining key metrics related to Business Strategy and Product Satisfaction. This in-depth analysis empowers users to make well-informed decisions aligned with their requirements. Based on the evaluation, the vendors are then categorized into four distinct quadrants representing varying levels of success: Forefront (F), Pathfinder (P), Niche (N), or Vital (V).
Market Share Analysis
The Market Share Analysis is a comprehensive tool that provides an insightful and in-depth examination of the current state of vendors in the Companion Diagnostics Market. By meticulously comparing and analyzing vendor contributions in terms of overall revenue, customer base, and other key metrics, we can offer companies a greater understanding of their performance and the challenges they face when competing for market share. Additionally, this analysis provides valuable insights into the competitive nature of the sector, including factors such as accumulation, fragmentation dominance, and amalgamation traits observed over the base year period studied. With this expanded level of detail, vendors can make more informed decisions and devise effective strategies to gain a competitive edge in the market.
Key Company Profiles
The report delves into recent significant developments in the Companion Diagnostics Market, highlighting leading vendors and their innovative profiles. These include Abbott Laboratories, Abnova Corporation, Agendia, Inc., Agilent Technologies, Inc., Almac Group, Amoy Diagnostics Co., Ltd., ARUP Laboratories, Bio-Techne Corporation, Biogenex Laboratories, Inc, bioMerieux SA, Danaher Corporation, Eli Lilly and Company, F. Hoffmann-La Roche AG, Guardant Health, Inc, ICON PLC, Illumina, Inc., Invivoscribe Technologies, Inc., Myriad Genetics, Inc., NG biotech, QIAGEN N.V., R-Biopharm AG, Siemens AG, Sysmex Corporation, and Thermo Fisher Scientific Inc..
Market Segmentation & Coverage
1. Market Penetration: It presents comprehensive information on the market provided by key players.
2. Market Development: It delves deep into lucrative emerging markets and analyzes the penetration across mature market segments.
3. Market Diversification: It provides detailed information on new product launches, untapped geographic regions, recent developments, and investments.
4. Competitive Assessment & Intelligence: It conducts an exhaustive assessment of market shares, strategies, products, certifications, regulatory approvals, patent landscape, and manufacturing capabilities of the leading players.
5. Product Development & Innovation: It offers intelligent insights on future technologies, R&D activities, and breakthrough product developments.
1. What is the market size and forecast of the Companion Diagnostics Market?
2. Which products, segments, applications, and areas should one consider investing in over the forecast period in the Companion Diagnostics Market?
3. What are the technology trends and regulatory frameworks in the Companion Diagnostics Market?
4. What is the market share of the leading vendors in the Companion Diagnostics Market?
5. Which modes and strategic moves are suitable for entering the Companion Diagnostics Market?