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The Patient Derived Xenograft/PDX Models Market size was estimated at USD 1.2 billion in 2023 and is projected to reach USD 2.6 billion by 2030, exhibiting a compound annual growth rate (CAGR) of 11.50% during the forecast period (2024-2030).
Study Period | 2018 - 2030 |
Base Year For Estimation | 2023 |
Forecast Data Period | 2024 - 2030 |
CAGR (2024-2030) | 11.50% |
2023 Market Size | USD 1.2 billion |
2030 Market Size | USD 2.6 billion |
Key Players | Charles River, The Jackson Laboratory, Crown Bioscience, WuXi AppTec, Champions Oncology |
The Patient Derived Xenograft (PDX) Models Market represents a critical segment within the biotechnology and pharmaceutical research landscape, primarily utilized for preclinical oncology drug development. These models are created by implanting tumor tissue from a patient directly into an immunodeficient mouse, which allows the tumor to retain the histological and genetic characteristics of the original malignancy. This high degree of fidelity makes PDX models superior to traditional cell line-derived xenografts for studying tumor biology, drug response, and resistance mechanisms. The market is characterized by its indispensable role in personalized medicine and translational research, enabling more accurate prediction of clinical outcomes. Key stakeholders include pharmaceutical companies, contract research organizations (CROs), academic research institutions, and biotechnology firms that leverage these models for target validation, biomarker discovery, and compound screening. The adoption of PDX models is integral to reducing drug attrition rates and enhancing the efficiency of oncology drug pipelines, thereby accelerating the development of novel therapeutics.
The Patient Derived Xenograft Models Market is distinguished by several key factors that underscore its scientific and commercial importance. A primary highlight is the models' ability to maintain the tumor microenvironment and heterogeneity, providing a more clinically relevant platform for drug testing compared to conventional models. This has positioned PDX models as a gold standard in preclinical cancer research. Furthermore, the market is witnessing increased collaboration between academic research centers and pharmaceutical companies to develop extensive and diverse PDX libraries, covering a wide array of cancer types and subtypes. The integration of advanced technologies such as next-generation sequencing and bioinformatics with PDX workflows is another significant highlight, enabling deeper molecular analysis and personalized treatment strategies. Companies like Charles River Laboratories, The Jackson Laboratory, and Crown Bioscience are at the forefront, offering comprehensive PDX model services and collections. The market's growth is also fueled by the rising prevalence of cancer and the subsequent demand for more effective and targeted therapies, making PDX models a cornerstone of modern oncology research and drug development.
The expansion of the Patient Derived Xenograft Models Market is propelled by several powerful drivers. A primary driver is the escalating global cancer incidence, which creates an urgent need for improved preclinical models that can accurately mimic human disease and predict therapeutic efficacy. The limitations of traditional cell line models, which often fail to recapitulate tumor complexity and lead to high drug failure rates in clinical trials, are a significant factor pushing the adoption of PDX systems. Additionally, substantial investments in oncology R&D from both public and private sectors are fueling market growth. The market presents substantial opportunities, particularly in the realm of co-clinical trials, where PDX models are used in parallel with clinical studies to guide patient treatment decisions. The emergence of humanized PDX models, which incorporate a human immune system, opens new avenues for immuno-oncology research and the development of immunotherapies. However, the market faces notable restraints. The high cost associated with developing and maintaining PDX models, coupled with technical challenges like long engraftment times and low success rates for certain cancer types, can hinder widespread adoption. Ethical concerns regarding the use of animal models also present a challenge, driving the need for continuous refinement of practices and exploration of alternative technologies.
The competitive landscape of the Patient Derived Xenograft Models Market is moderately concentrated, with a mix of established players and specialized niche providers dominating the space. A handful of leading companies control a significant portion of the market share through their extensive model collections, robust service portfolios, and strong global presence. These key players, including Charles River Laboratories, Crown Bioscience (a JSR Life Sciences company), The Jackson Laboratory, and Champions Oncology, have built their leadership by investing heavily in building large, well-characterized PDX libraries and offering integrated drug discovery services. Their strategies often involve forming strategic alliances with pharmaceutical giants and academic institutions to enhance their model repositories and technological capabilities. Alongside these leaders, numerous smaller biotechnology firms and academic spin-offs are contributing to the market by focusing on specific cancer types or innovative model engineering, such as humanized PDX systems. This concentration dynamic fosters an environment of both competition and collaboration, driving advancements in model quality and application scope while ensuring that end-users have access to a diverse range of high-fidelity research tools.
The Patient Derived Xenograft Models Market can be segmented based on model type, primarily into mice models and rat models, with mice models constituting the vast majority of the market. Immunodeficient mouse strains, such as NOD scid gamma (NSG) and athymic nude mice, are the most commonly used hosts due to their severely compromised immune systems, which prevent rejection of human tumor tissue and allow for successful engraftment and growth. Within mice models, there is further diversification into subtypes like humanized PDX models, which are engineered to possess a functional human immune system. These humanized models are gaining tremendous traction as they enable the study of tumor-immune cell interactions and the evaluation of immunotherapies, including checkpoint inhibitors and CAR-T cells, in a more physiologically relevant context. The development of these advanced model types addresses a critical gap in immuno-oncology research and represents a significant innovation within the market, catering to the evolving needs of cancer drug developers.
PDX models find extensive application across the entire spectrum of preclinical oncology research and drug development. Their primary application is in drug discovery and development, where they are used for pharmacodynamic studies, efficacy testing of novel therapeutic compounds, and biomarker identification. Pharmaceutical companies heavily rely on these models to prioritize lead candidates before advancing them to costly clinical trials. Another critical application is in basic cancer research, where academic institutions utilize PDX models to investigate tumor biology, metastasis, and mechanisms of drug resistance. The models are also indispensable in the burgeoning field of personalized medicine, particularly in the form of co-clinical trials. In this approach, PDX models are generated from individual patients enrolled in a clinical trial, allowing researchers to test various drug combinations on the avatars to identify the most effective therapeutic strategy for that specific patient, thereby guiding clinical decision-making and improving outcomes.
The global Patient Derived Xenograft Models Market exhibits distinct regional patterns in terms of adoption, research activity, and market presence. North America, led by the United States, holds the largest market share. This dominance is attributed to the presence of a robust biotechnology and pharmaceutical industry, high levels of R&D funding from both federal agencies like the NIH and private investors, and a concentration of leading academic research institutions and CROs specializing in preclinical models. Europe represents another significant market, with strong research activities in countries such as the United Kingdom, Germany, and France, supported by collaborative EU-funded research initiatives. The Asia Pacific region is identified as the fastest-growing market, driven by increasing government and private investment in life sciences, a rising burden of cancer, and the expansion of contract research capabilities in countries like China and Japan. This regional growth is fostering the development of local PDX model repositories and services, making advanced research tools more accessible across the globe.
The competitive environment in the PDX models market features several prominent companies that have established themselves through innovation, scale, and service quality. Charles River Laboratories International Inc. is a global leader, offering a vast portfolio of PDX models and related in vivo services to support oncology programs. Crown Bioscience, a part of JSR Life Sciences, is renowned for its extensive collection of well-characterized PDX models, its HuPrime? platform, and its integrated translational research services. The Jackson Laboratory, a non-profit biomedical research institution, provides a large repository of PDX models through its JAX? PDX resource, supporting both academic and industrial research. Champions Oncology differentiates itself with its personalized PDX platform, often referred to as TumorGrafts?, which it uses to support both drug discovery and personalized medicine approaches for individual patients. Other notable players include WuXi AppTec and Hera Biolabs, which contribute significantly to the market with their specialized offerings and growing model collections.
The Patient Derived Xenograft Models Market is dynamic, with continuous recent developments focused on enhancing model utility and expanding applications. A major trend is the rapid advancement in humanized PDX models. Companies are increasingly developing more sophisticated models with engrafted human immune systems to better evaluate the efficacy and safety of immunooncology therapeutics, which represent a dominant area of drug development. Another significant development is the strategic expansion of PDX model libraries to include rare and pediatric cancers, addressing unmet needs in these challenging disease areas. Furthermore, there is a growing emphasis on the integration of multi-omics data?including genomic, transcriptomic, and proteomic profiles?with PDX model data to create deeply annotated resources that provide richer insights into drug response mechanisms. Collaboration and partnership activities remain high, with CROs and biotech firms entering into agreements with pharmaceutical companies to provide exclusive or broad access to their PDX platforms for target validation and drug screening campaigns, thereby accelerating the pace of oncology innovation.
This comprehensive market research report on the Patient Derived Xenograft Models Market provides a detailed analysis segmented across multiple dimensions to offer a granular view of the industry landscape. The segmentation is designed to help stakeholders understand specific market dynamics and identify targeted opportunities. The report is segmented by model type, distinguishing between mice models and rat models, with further breakdowns into subtypes such as humanized PDX models. It is also segmented by application, covering critical areas such as drug discovery & development, basic cancer research, and personalized medicine. The tumor type segmentation provides insights into demand patterns for models of solid tumors versus hematological malignancies, and further into specific cancers like lung, breast, gastrointestinal, and others. Furthermore, the report includes a detailed segmentation by end-user, analyzing the market for academic & research institutions, pharmaceutical & biotechnology companies, and contract research organizations. Each segment is analyzed in terms of adoption trends, growth influencers, and competitive landscape, providing a strategic tool for informed decision-making.
What are Patient Derived Xenograft (PDX) models?
Patient Derived Xenograft models are advanced preclinical research tools created by transplanting tumor tissue from a cancer patient directly into an immunodeficient mouse. This process allows the tumor to grow and retain the key genetic and histological characteristics of the original human cancer, providing a highly representative platform for studying disease biology and testing new therapies.
How are PDX models used in drug discovery?
In drug discovery, PDX models are extensively used to evaluate the efficacy and safety of novel oncology compounds before they enter human clinical trials. Researchers can test various drug doses and combinations on these models to identify promising candidates, understand mechanisms of action, and discover predictive biomarkers that can guide clinical development strategies and improve trial success rates.
What are the advantages of using PDX models over cell line models?
PDX models offer significant advantages over traditional cell line-derived xenografts. They preserve the tumor's heterogeneity, stromal architecture, and genetic profile of the original patient tumor, which is often lost in cell culture. This leads to more clinically predictive data regarding drug response and resistance, making them a superior tool for translational research and reducing the high attrition rates common in oncology drug development.
What is the difference between CDX and PDX models?
The fundamental difference lies in the origin of the tumor tissue. Cell Line-Derived Xenograft (CDX) models are established by implanting immortalized cancer cell lines into mice, which have been adapted to grow in vitro and may not fully represent original tumors. Patient-Derived Xenograft (PDX) models use tumor tissue taken directly from a patient, maintaining a much higher degree of biological fidelity and clinical relevance.
What are humanized PDX models?
Humanized PDX models are an advanced type of PDX model where the immunodeficient mouse host is engrafted with functional human immune cells or stem cells to recreate a human immune system. This allows researchers to study the complex interactions between the human tumor and the human immune system, making these models particularly valuable for developing and testing immunotherapies like checkpoint inhibitors.
Which companies are the leading providers of PDX models?
The market is served by several leading providers known for their extensive model collections and service expertise. Key companies include Charles River Laboratories, Crown Bioscience, The Jackson Laboratory, and Champions Oncology. These firms offer comprehensive portfolios of well-characterized PDX models across various cancer types and provide integrated drug discovery and development services to the global pharmaceutical and biotechnology industry.
Citius Research has developed a research report titled “Patient Derived Xenograft/PDX Models Market Report - Global Industry Analysis, Size, Share, Growth Trends, Regional Outlook, Competitive Strategies and Segment Forecasts 2024 - 2030” delivering key insights regarding business intelligence and providing concrete business strategies to clients in the form of a detailed syndicated report. The report details out the factors such as business environment, industry trend, growth opportunities, competition, pricing, global and regional market analysis, and other market related factors.
• Patient Derived Xenograft/PDX Models Market Potential
• Segment-wise breakup
• Compounded annual growth rate (CAGR) for the next 6 years
• Key customers and their preferences
• Market share of major players and their competitive strength
• Existing competition in the market
• Price trend analysis
• Key trend analysis
• Market entry strategies
• Market opportunity insights
The report focuses on the drivers, restraints, opportunities, and challenges in the market based on various factors geographically. Further, key players, major collaborations, merger & acquisitions along with trending innovation and business policies are reviewed in the report. The Patient Derived Xenograft/PDX Models Market report is segmented on the basis of various market segments and their analysis, both in terms of value and volume, for each region for the period under consideration.
• North America
• Latin America
• Europe
• MENA
• Asia Pacific
• Sub-Saharan Africa and
• Australasia
The report covers below mentioned analysis, but is not limited to:
• Overview of Patient Derived Xenograft/PDX Models Market
• Research Methodology
• Executive Summary
• Market Dynamics of Patient Derived Xenograft/PDX Models Market
• Driving Factors
• Restraints
• Opportunities
• Global Market Status and Forecast by Segment A
• Global Market Status and Forecast by Segment B
• Global Market Status and Forecast by Segment C
• Global Market Status and Forecast by Regions
• Upstream and Downstream Market Analysis of Patient Derived Xenograft/PDX Models Market
• Cost and Gross Margin Analysis of Patient Derived Xenograft/PDX Models Market
• Patient Derived Xenograft/PDX Models Market Report - Global Industry Analysis, Size, Share, Growth Trends, Regional Outlook, Competitive Strategies and Segment Forecasts 2024 - 2030
• Competition Landscape
• Market Share of Major Players
• Key Recommendations
The “Patient Derived Xenograft/PDX Models Market Report - Global Industry Analysis, Size, Share, Growth Trends, Regional Outlook, Competitive Strategies and Segment Forecasts 2024 - 2030” report helps the clients to take business decisions and to understand strategies of major players in the industry. The report delivers the market driven results supported by a mix of primary and secondary research. The report provides the results triangulated through authentic sources and upon conducting thorough primary interviews with the industry experts. The report includes the results on the areas where the client can focus and create point of parity and develop a competitive edge, based on real-time data results.
Below are the key stakeholders for the Patient Derived Xenograft/PDX Models Market:
• Manufacturers
• Distributors/Traders/Wholesalers
• Material/Component Manufacturers
• Industry Associations
• Downstream vendors
Report Attribute | Details |
Base year | 2023 |
Historical data | 2018 – 2023 |
Forecast | 2024 - 2030 |
CAGR | 2024 - 2030 |
Quantitative Units | Value (USD Million) |
Report coverage | Revenue Forecast, Competitive Landscape, Growth Factors, Trends and Strategies. Customized report options available on request |
Segments covered | Product type, technology, application, geography |
Regions covered | North America, Latin America, Europe, MENA, Asia Pacific, Sub-Saharan Africa and Australasia |
Countries covered | US, UK, China, Japan, Germany, India, France, Brazil, Italy, Canada, Russia, South Korea, Australia, Spain, Mexico and others |
Customization scope | Available on request |
Pricing | Various purchase options available as per your research needs. Discounts available on request |
Like most other markets, the outbreak of COVID-19 had an unfavorable impact on the Patient Derived Xenograft/PDX Models Market worldwide. This report discusses in detail the disruptions experienced by the market, the impact on flow of raw materials, manufacturing operations, production trends, consumer demand and the projected future of this market post pandemic.
The report has helped our clients:
• To describe and forecast the Patient Derived Xenograft/PDX Models Market size, on the basis of various segmentations and geography, in terms of value and volume
• To measure the changing needs of customers/industries
• To provide detailed information regarding the drivers, restraints, opportunities, and challenges influencing the growth of the market
• To gain competitive intelligence and uncover new opportunities
• To analyse opportunities in the market for stakeholders by identifying high-growth segments in Patient Derived Xenograft/PDX Models Market
• To strategically profile key players and provide details of the current competitive landscape
• To analyse strategic approaches adopted by players in the market, such as product launches and developments, acquisitions, collaborations, contracts, expansions, and partnerships
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We follow a robust research methodology to analyze the market in order to provide our clients with qualitative and quantitative analysis which has a very low or negligible deviance. Extensive secondary research supported by primary data collection methods help us to thoroughly understand and gauge the market. We incorporate both top-down and bottom-up approach for estimating the market. The below mentioned methods are then adopted to triangulate and validate the market.
Secondary research includes sources such as published books, articles in journals, news media and published businesses, government and international body publications, and associations. Sources also include paid databases such as Hoovers, Thomson Reuters, Passport and others. Data derived through secondary sources is further validated through primary sources. The secondary sources also include major manufacturers mapped on the basis of revenues, product portfolios, and sales channels.
Primary data collection methods include conducting interviews with industry experts and various stakeholders across the supply chain, such as raw material suppliers, manufacturers, product distributors and customers. The interviews are either telephonic or face-to-face, or even a combination of both. Prevailing trends in the industry are gathered by conducting surveys. Primary interviews also help us to understand the market drivers, restraints and opportunities, along with the challenges in the market. This method helps us in validating the data gathered through secondary sources, further triangulating the data and developing it through our statistical tools. We generally conduct interviews with -
Supply side analysis is based on the data collected from the manufacturers and the product providers in terms of their segmental revenues. Secondary sources for this type of analysis include company annual reports and publications, associations and organisations, government publications and others.
Demand side analysis is based upon the consumer insights who are the end users of the particular product in question. They could be an individual user or an organisation. Such data is gathered through consumer surveys and focused group interviews.
As a primary step, in order to develop the market numbers we follow a vigorous methodology that includes studying the parent market of the niche product and understanding the industry trends, acceptance among customers of the product, challenges, future growth, and others, followed by further breaking down the market under consideration into various segments and sub-markets. Additionally, in order to cross-validate the market, we also determine the top players in the market, along with their segmental revenues for the said market. Our secondary sources help us to validate the market share of the top players. Using both the qualitative and quantitative analysis of all the possible factors helps us determine the market numbers which are inclined towards accuracy.
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