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市场调查报告书
商品编码
1371955
2030 年生物标记市场预测:按产品类型、适应症、服务、用途、最终用户和地区进行的全球分析Biomarker Market Forecasts to 2030 - Global Analysis By Product (Consumables, Software and Services), Type (Safety Biomarkers, Validation Biomarkers and Efficacy Biomarkers), Indication, Service, Application, End User and By Geography |
根据 Stratistics MRC 的数据,2023 年全球生物标记市场规模为 581.2 亿美元,预计到 2030 年将达到 1,102.4 亿美元,预测期内年复合成长率为 14.2%。
生物标记是生物标记的简称,指检测、可量化的生物参数或特征,是生理或病理过程、疾病状态或治疗反应的指标。生物标记存在于多种生物样本中,包括血液、尿液、组织和其他体液。生物标记包括广泛的属性,包括遗传变异、基因表现模式、蛋白质水平、酶活性、代谢物浓度和影像特征。
根据中国卫生署公布的资料,约有2.03亿人患有心血管疾病,预计2030年这数字将增加73%。
癌症是一种复杂的疾病,由阶段致癌过程引起,涉及多个分子途径事件,使诊断、预后和治疗变得困难。癌症很复杂,因此没有单一的标记物是有效的。此外,不同类型的癌症具有不同的分子特征。新型生物标记的鉴定为开发旨在纠正癌症失调的治疗方法开闢了新途径。因此,由于生物标记研究的开拓和癌症罹患率的上升,全球市场预计将扩大。
生物标誌物市场实行严格的规则和法规,以在医疗保健提供者、患者和相关人员之间建立信任和信心。这对于广泛采用基于生物标记的诊断和治疗至关重要。法规促进了生物标记开发、检验和应用的标准化。这些法规的复杂性使得它们对于做出资讯的医疗决策至关重要。因此,这个因素阻碍了市场的成长。
个人化医疗依赖于识别患者疾病的特定遗传、分子和生化特征的生物标记。这些生物标记有助于确定最有效的治疗方法并最大限度地减少试验的需要。个人化医疗旨在透过根据每位患者的生物体质制定治疗方案来提高治疗效果。以生物标记为指导的个人个人化医疗可以根据患者的个别特征客製化药物给药和治疗方法,从而优化治疗结果。它透过提高患者参与度和满意度来推动市场成长,从而实现早期疾病检测和预防。
生物标誌物的开发需要大量资金和涉及科学家、临床医生、法规专家和其他专家的多学科方法。高开发成本反映了将可靠的生物标记物引入临床所需的复杂性和严格性。此外,生物标誌物的开发通常涉及一个漫长的迭代过程。此外,维持高品质品质、僱用熟练的科学家和建造技术基础设施都会产生额外的成本,从而阻碍市场需求。
COVID-19 大流行将对生物标记物产业产生适度的正面影响,因为生物标记物对于为 COVID-19 患者创造治疗方法至关重要。许多研究发现生物标记对于诊断和治疗至关重要。此外,一些组织还宣布了用于鉴定和治疗 COVID-19 的生物标记产品。这些新兴市场的开拓使得市场在疫情期间不断扩大。
癌症领域预计将出现良好的成长。生物标记在癌症诊断、预后和治疗中发挥重要作用。生物标记是检测的生物指标,可以提供有关癌症的存在、进展以及对某些治疗的反应性的资讯。它有助于鉴定肿瘤的特定分子或遗传特征,从而可以选择更有效的标靶治疗。从早期检测到治疗方法选择、监测和监测,生物标记有助于为癌症诊断和治疗提供更个体化和有效的方法。
诊断与研究实验室领域预计在预测期内将以最高的年复合成长率成长。诊断实验室在监测疾病进展和评估治疗效果方面发挥重要作用。诊断和研究实验室在生物标记领域的进步中发挥着至关重要的作用。我们参与生物标记开发和应用过程的每阶段,从生物标记发现和检验到临床试验、检测开发和患者照护。他们的工作对诊断疾病、选择治疗方法和改善患者的治疗效果做出了重大贡献。
由于高疾病负担、消费者对生物标记的认识不断提高、政府配合措施、技术突破和医疗保健基础设施的改善,预计北美在预测期内将占据最大的市场占有率。事实确实如此。在北美,美国占有最大的市场占有率。预计推动该地区成长的关键因素是该领域知名公司的存在以及他们正在进行的许多有机和无机项目。
由于癌症罹患率、研究计画不断增加和临床试验成本低,预计亚太地区在预测期内将呈现最高的年复合成长率。生物标记在药物研发和药物开发过程中的应用正在推动新生物标记开发的研究投资。此外,对生物技术和製药公司的资助增加、合约研究组织数量的增加以及生物标誌物应用范围的扩大预计将在预测期内推动区域市场的成长。
According to Stratistics MRC, the Global Biomarker Market is accounted for $58.12 billion in 2023 and is expected to reach $110.24 billion by 2030 growing at a CAGR of 14.2% during the forecast period. A biomarker, short for biological marker, refers to a measurable and quantifiable biological parameter or characteristic that serves as an indicator of a physiological or pathological process, a disease state, or a response to treatment. Biomarkers can be found in various biological samples, such as blood, urine, tissue, or other bodily fluids. Biomarkers can encompass a wide range of attributes, including genetic mutations, gene expression patterns, protein levels, enzyme activity, metabolite concentrations, and imaging features.
According to data published by ministry of health in China, about 203 million people are suffering from cardiovascular diseases and this number is expected to increase by 73% in 2030.
Cancer is a complicated illness caused by a multi-stage carcinogenesis process with several molecular pathway events that make diagnosis, prognosis, and treatment difficult. A single marker is ineffective because cancer is complicated. Additionally, each kind of cancer has a unique molecular profile from the others. The identification of novel biomarkers opens up new avenues for the development of treatment approaches intended to correct dysregulation in cancer. As a result, the worldwide market will expand due to the development of biomarker research and the rising incidence of cancer.
Strict rules and regulations are imposed to help build confidence and trust among healthcare providers, patients, and stakeholders in the biomarker market. This is crucial for the widespread adoption of biomarker-based diagnostics and therapies. Regulations promote standardization in the development, validation, and application of biomarkers. These regulations are complex and therefore become critical for making uninformed medical decisions. Thereby, this element hampers the market growth.
Personalized medicine relies on biomarkers to identify specific genetic, molecular, or biochemical characteristics of a patient's disease. These biomarkers help determine the most effective treatment options, minimizing the need for trial-and-error approaches. By tailoring treatments to the individual patient's biological makeup, personalized medicine aims to increase treatment efficacy. Personalized medicine, guided by biomarkers, allows for the customization of drug dosage and treatment regimens based on individual patient characteristics, optimizing therapeutic outcomes. Its greater patient engagement and satisfaction followed up by early disease detection and prevention fuels the market growth.
The development of biomarkers requires significant financial investment and a multidisciplinary approach involving scientists, clinicians, regulatory experts, and other professionals. The high development costs reflect the complexity and rigor required to bring reliable biomarkers to clinical practice. Also, biomarker development often involves long and iterative processes; this prolonged timeline can result in cumulative costs. In addition, maintaining high standards of quality, recruiting skilled scientists and setting up technological infrastructure adds extra expenses which hinder the market demand.
The COVID-19 pandemic has a moderately beneficial effect on the biomarkers industry since biomarkers are essential for the creation of COVID-19 patient therapeutics. Biomarkers were discovered to be essential in the diagnosis and therapy in a number of studies. In addition, several organisations have introduced biomarker products to identify and treat COVID-19. These developments caused the market to expand throughout the pandemic era.
The cancer segment is estimated to have a lucrative growth. Biomarkers play a crucial role in the diagnosis, prognosis, and treatment of cancer. They are measurable biological indicators that can provide information about the presence or progression of cancer, as well as the likely response to specific treatments. It can help identify specific molecular or genetic characteristics of a tumor, allowing for the selection of targeted therapies that are more likely to be effective. From early detection to treatment selection, monitoring and research, biomarker contributes to more personalized and effective approaches to cancer diagnosis and treatment.
The diagnostics & research laboratories segment is anticipated to witness the highest CAGR growth during the forecast period. Diagnostic labs play a vital role in monitoring disease progression and evaluating the effectiveness of treatments. Diagnostics and research laboratories play a pivotal role in advancing the field of biomarkers. They are involved in every stage of the biomarker development and application process, from discovery and validation to clinical testing, assay development, and patient care. Their work contributes significantly to improving disease diagnosis, treatment selection, and patient outcomes.
North America is projected to hold the largest market share during the forecast period owing to the high disease burden, rising consumer awareness of biomarkers, encouraging government efforts, technical breakthroughs, and improvements in healthcare infrastructure. In North America, the United States holds the largest market share. A significant element anticipated to fuel the region's growth is the presence of prominent firms in this area and the many organic and inorganic projects they have undertaken.
Asia Pacific is projected to have the highest CAGR over the forecast period, owing to its high prevalence of cancer, rising research initiatives, and low cost of clinical trials. Application of biomarkers in the drug discovery and development process is boosting key market players to invest in the research to develop novel biomarkers. In addition, an increase in funding for biotech and pharma companies, a rise in the number of CROs, and an increasing application scope of biomarkers are expected to facilitate regional market growth during the projected period.
Some of the key players profiled in the Biomarker Market include: GE Healthcare, Aushon Biosystem, Eisai Co. Limited, Abbott Laboratories, Inc., Epistem Limited, Agilent Technologies Inc., Roche Diagnostics Limited, Siemens AG, Bio-Rad Laboratories, Thermo Fisher Scientific Inc., Johnson & Johnson Services, Inc., Epigenomics AG, QIAGEN, Enzo Biochem Inc, Charles River Laboratories International Inc., Eurofins Scientific, LifeSign LLC, Bruker, Sino Biological Inc and Quest Diagnostics Incorporated.
In November 2022, Siemens is expanding its generator circuit-breaker portfolio with a new compact version - the HB1-Compact (HB1-C). The versatile and highly customizable solution uses maintenance-free vacuum switching technology and addresses the most challenging of constraints.
In September 2022, GE Healthcare, a medical technology, diagnostics, and digital solutions company, launched its 'Made in India', 'AI-powered' Cath lab-Optima IGS 320 to advance cardiac care in India. It is built at Wipro GE Healthcare's new Bengaluru factory and leverages the GE proprietary AutoRight technology.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.