市场调查报告书
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1470514
临床试验市场:按设计、阶段和适应症划分 - 2024-2030 年全球预测Clinical Trials Market by Design (Interventional Study, Observational Study), Phase (Phase I, Phase II, Phase III), Indication - Global Forecast 2024-2030 |
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预计2023年临床试验市场规模为383亿美元,预计2024年将达417.8亿美元,2030年将达到707.8亿美元,复合年增长率为9.16%。
临床试验是一项研究活动,旨在调查新的测试和治疗方法并评估其对健康的影响。它允许人们参与医疗干预措施的测试,包括药物、细胞和其他生物产品、外科手术、放射治疗、设备、行为疗法和预防性医疗保健。对慢性病和感染疾病的担忧使得学名药和生物製药的开发和商业化受到重视,从而增加了对临床试验的需求。製药和生物技术行业对药物开发活动的日益关注以及研发支出的增加正在推动对临床试验的需求。然而,与临床试验活动相关的高成本和严格的政府法规减缓了药物开发和研究活动。公司专注于降低成本,同时提供创新的调查方法。此外,全球对药物开发的关注和向以患者为中心的临床试验的转变、临床试验全球化的迅速发展以及监管协调性和透明度的提高正在推动创新并改善患者的健康和福祉。
主要市场统计 | |
---|---|
基准年[2023] | 383亿美元 |
预测年份 [2024] | 417.8亿美元 |
预测年份 [2030] | 707.8亿美元 |
复合年增长率(%) | 9.16% |
设计 介入性和观察性临床试验设计对于优化治疗效果、风险和安全性评估的重要性
介入性研究和观察性研究是 KEYWORD 的两种不同的研究方法,它们具有不同的目的来推进医学知识。在介入研究中,研究人员为参与者分配特定的治疗或介入措施,例如适应试验、非随机对照试验或随机对照试验,并评估对健康结果的影响。此外,观察性研究允许研究人员在不干扰受试者护理的情况下观察受试者,并检查横断面活动、对照和生态学研究等暴露之间的关联。儘管干预研究由于其受控环境而提供了更高程度的证据,但它们可能昂贵、耗时且在伦理上受到限制。另一方面,观察性研究反映了现实世界的情况,因此提供了更具普遍性的结果,但由于不受控制的混杂因素而更容易出现偏差。
阶段:临床试验监测药物代谢和收集初始资料的阶段。
临床试验对于新治疗方法、药物和设备的开发和核准至关重要。这些临床试验由多个阶段组成,并遵循规范的流程,以确保安全性、有效性以及适当的剂量和给药。 II 期试验透过确定药物或治疗方法对患有特定疾病的患者是否具有治疗效果来评估药物或治疗方法的有效性。 III 期试验(临床试验)是对数百至数千人的不同族群进行的大规模试验。此阶段的目的是在不同环境和地点的更广泛患者群体中确认治疗的安全性和有效性。 IV期试验(临床试验)是在药物获得监管机构核准并投放市场后进行的。这些试验旨在监测更多人群的长期安全性和有效性,同时继续评估药物的副作用和潜在的新用途。
适应症:针对慢性病、心血管疾病和其他有害疾病提出适当治疗方法和药物的一些适应症
临床试验广泛描述疾病和状况,并协助研究人员进行药物、手术和治疗。自体免疫临床试验为涉及慢性和有害发炎的疾病提供了参考。本研究旨在确定患者和健康个体自体免疫疾病和发炎疾病的生物标记。心血管疼痛临床试验揭示了调节心房-心室(AV)和心室间(VV)时间延迟对运动期间心臟血流动力学的影响。中枢神经系统临床试验检查来自接受过各种手术(包括脑炎和脊髓炎)的受试者的配对血清和脑脊髓液样本,以调查疑似感染或发炎的具体途径。此外,人类疾病、糖尿病和肿瘤学方面的临床试验有助于研究人员了解患者的免疫系统对疾病的反应,并有助于预防疾病和改善治疗方法。
区域洞察
由于癌症诊断和心血管疾病的需求不断增加,美洲临床试验的扩展得到了显着改善。许多监管机构,例如美国食品药物管理局(FDA) 和国家卫生管理局 (ANVISA),建立了药物开发的法规结构并确保所进行的临床试验的品质。在墨西哥、阿根廷和巴西等新兴国家,政府正在进行大量投资,鼓励研发和技术进步,以支持医疗保健基础设施的发展。由于中国、印度、韩国、台湾、印尼和越南等国家製药业的发展,亚太临床试验市场正在快速成长。近年来,澳洲和纽西兰对生物技术和製药产业的投资有所增加,并且作为新兴经济体,临床试验活动显着成长。由于拥有大量的製药和生物技术公司,欧洲长期以来一直被认为是全球临床试验的战场。欧盟 (EU) 制定了在其成员国内进行临床试验的既定框架,以确保临床实验药物的安全性、有效性和品质。
FPNV定位矩阵
FPNV定位矩阵对于评估临床试验市场至关重要。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,可以对临床试验市场中供应商的现状进行深入而深入的研究。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。这种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. 竞争评估和情报:对主要企业的市场占有率、策略、产品、认证、监管状况、专利状况和製造能力进行全面评估。
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.临床试验市场的市场规模与预测是多少?
2.临床试验市场预测期内需要考虑投资的产品、细分市场、应用和领域有哪些?
3.临床试验市场的技术趋势和法规结构是什么?
4.临床试验市场主要厂商的市场占有率为何?
5. 进入临床试验市场的合适型态或策略手段是什么?
[184 Pages Report] The Clinical Trials Market size was estimated at USD 38.30 billion in 2023 and expected to reach USD 41.78 billion in 2024, at a CAGR 9.16% to reach USD 70.78 billion by 2030.
Clinical trials are research activities that study new tests and treatments and evaluate effects on human health outcomes. It allows people to participate in testing medical interventions, including drugs, cells, other biological products, surgical procedures, radiological procedures, devices, behavioral treatments, and preventive care. The increased focus on developing and commercializing generics and biologics due to concerns related to chronic and infectious diseases increases demand for clinical trials. The growing emphasis on drug development activities and rising research and development expenditure from the pharmaceutical and biotechnology industry enhances the demand for clinical trials. However, the significant cost associated with clinical trial activities and stringent government regulations slow down drug development and research activities. Companies are focusing on cutting a cost alongside providing innovative research methodologies. Moreover, the worldwide focus on drug development and shift towards patient-centric clinical trials alongside rapidly improving globalization of clinical trials and greater regulatory harmonization and transparency promote innovation and better patient health and welfare.
KEY MARKET STATISTICS | |
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Base Year [2023] | USD 38.30 billion |
Estimated Year [2024] | USD 41.78 billion |
Forecast Year [2030] | USD 70.78 billion |
CAGR (%) | 9.16% |
Design: Importance of interventional and observational clinical trial design to optimize assessment of treatment efficacy, risk, and safety
Interventional and observational studies are two distinct research approaches in clinical trials, serving different purposes in advancing medical knowledge. Interventional studies involve researchers assigning participants to specific treatments and interventions such as adaptive clinical trials, non-randomized control trials, and randomized control trials to assess their effects on health outcomes. Additionally, observational studies involve researchers observing subjects without interfering in their care to examine associations between exposures, including cross-sectional activities, control, and ecological study. Interventional studies provide higher levels of evidence due to their controlled settings but can be expensive, time-consuming, and ethically limited. On the other hand, observational studies offer more generalizable results since they reflect real-world conditions but are prone to biases from uncontrolled confounding factors.
Phase: clinical trial phases in for monitoring drug metabolism and gathering initial data
Clinical trials are essential in developing and approving new medical treatments, drugs, and devices. These trials follow a structured and regulated process with different phases ensuring safety, efficacy, and appropriate dosage. In Phase II, researchers evaluate effectiveness by determining whether or not the drug or treatment produces therapeutic benefits in patients with specific medical conditions. Phase III clinical trials are large-scale studies conducted on a diverse population ranging from several hundred to several thousand participants. This phase aims to confirm the safety and efficacy of a treatment in a broader patient population under different settings and locations. Phase IV clinical trials occur after a drug has been approved by regulatory authorities and released into the market. These trials aim to monitor long-term safety and effectiveness in a larger population while continuing to evaluate the drug's side effects and potential new uses.
Indication: Several indications suggesting suitable treatments and medications for chronic, cardiovascular, and other harmful diseases
Clinical trials widely indicate a disease or symptom and help researchers with medication, procedure, and treatment. Clinical trials of Autoimmune help learn more about conditions with chronic and harmful inflammation. This study aims to identify biomarkers in people with autoimmune or inflammatory diseases and healthy people. Clinical trial in cardiovascular pain helps to determine the results of adjusting atrial-ventricular (AV) and interventricular (VV) timing delays on cardiac hemodynamics during exercise. Clinical trials in CNS examine paired serum and cerebrospinal fluid samples from subjects with various procedures, including encephalitis and myelitis, to investigate specific pathways of suspected infection and inflammation. In addition, clinical trials involved in the human condition, diabetes, and oncology help researchers understand the patient's immune system response to a disease and work to prevent it and improve its treatment.
Regional Insights
The growing expansion of clinical trials in the Americas significantly improved due to the increasing need for cancer diagnostic and cardiovascular diseases. Many regulatory organizations, such as the United States Food and Drug Administration (FDA) and the National Health Surveillance Agency (ANVISA), establish regulatory frameworks for drug development to ensure the quality of clinical trials conducted. In developing countries such as Mexico, Argentina, and Brazil, governments are making considerable investments to encourage research and technological advancements to boost the development of medical & healthcare infrastructure. The Asia-Pacific region's clinical trial market is growing rapidly due to its evolving pharmaceutical industry in some countries, including China, India, South Korea, Taiwan, Indonesia, and Vietnam. In recent years, the growing investments in biotechnology and pharmaceutical industries in Australia and New Zealand have shown significant growth in clinical trial activities due to their emerging economies. Europe has been considered a rampart place for the global clinical trial due to the presence of numerous pharmaceutical and biotechnology companies. The European Union (EU) has a well-established framework for conducting clinical trials across its member states that ensures the safety, efficacy, and quality of investigational medicinal products.
FPNV Positioning Matrix
The FPNV Positioning Matrix is pivotal in evaluating the Clinical Trials 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 Clinical Trials 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 Clinical Trials Market, highlighting leading vendors and their innovative profiles. These include Accell Clinical Research, LLC, Atlant Clinical Ltd., Becton, Dickinson and Company, Bio-Rad Laboratories, Inc., Bristol-Myers Squibb Company, Charles River Laboratories International, Inc., Clinipace, Congenix LLP, Eli Lilly and Company, Icon PLC, Illumina, Inc, IQVIA Holdings, Inc., Labcorp, Merck KGaA, Novo Nordisk A/S, Parexel International Corporation, Pfizer Inc., ProPharma Group Holdings, LLC, Qiagen NV, Sartorius AG, SGS S.A., SIRO Clinpharm Private Limited, Syneos Health, Inc., Thermo Fisher Scientific Inc., and Wuxi AppTec 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 Clinical Trials Market?
2. Which products, segments, applications, and areas should one consider investing in over the forecast period in the Clinical Trials Market?
3. What are the technology trends and regulatory frameworks in the Clinical Trials Market?
4. What is the market share of the leading vendors in the Clinical Trials Market?
5. Which modes and strategic moves are suitable for entering the Clinical Trials Market?