Netherlands Oncology Clinical Trials Market Analysis

Netherlands Oncology Clinical Trials Market Analysis


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Netherlands oncology clinical trials Market is projected to grow from $32.9 Mn in 2022 to $52.4 Mn by 2030, registering a CAGR of 6% during the forecast period of 2022-30. The market will be driven by the country's strong healthcare system, experienced clinical researchers, and a supportive government. The market is segmented by phase, by study design & by indication. Some of the major players include Roche Holding AG, Pfizer Inc & Kiadis Pharma.

ID: IN10NLCT006 CATEGORY: Clinical Trials GEOGRAPHY: Netherlands AUTHOR: Vidhi Upadhyay

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Netherlands Oncology Clinical Trials Market Executive Summary

Netherlands oncology clinical trials Market is projected to grow from $32.9 Mn in 2022 to $52.4 Mn by 2030, registering a CAGR of 6% during the forecast period of 2022-30. The most prevalent malignancies among women in the Netherlands are lung, colon, and breast cancer. In 2022, 124.109 people were diagnosed with cancer: 65.591 males and 58.518 women. In the Netherlands, more than 850.000 people have cancer or have survived cancer. The Netherlands was one of the first nations to establish a cancer institute: the Netherlands Cancer Institute (NKI). The NKI, which was founded in 1913, is today one of the world's greatest comprehensive cancer centers.

Many oncology clinical trials are now underway in the Netherlands. These studies are intended to put innovative cancer treatments, therapies, and diagnostic technologies to the test. These studies are taking place in many medical facilities and hospitals around the Netherlands, including the Erasmus Medical Center, the University Medical Center Utrecht, and the Netherlands Cancer Institute. The Netherlands has a well-developed healthcare system and a solid research infrastructure, making it a suitable site for clinical trials. The nation also boasts a highly educated populace, with many people eager to take part in clinical trials to enhance medical knowledge and improve cancer treatment choices.

netherlands oncology clinical trials market anlaysis

Market Dynamics

Market Growth Drivers

Oncode Institute, one of the biggest strategic public-private collaborations in the Netherlands, brings together 800+ exceptional cancer researchers from 12 universities, academic hospitals, and research organizations. The Netherlands is leading in oncology not only in Europe, but across the globe, owing to innovative prevention, diagnostics, and therapies nurtured in a connected and collaborative environment. According to recent research, the Netherlands is the second-best country in the world for cancer treatment and the best in Europe. With over 500 public-private collaborations, a key location for R&D cooperation, and accessibility for Europeans seeking treatment – as well as solid logistics to simplify manufacture and distribution worldwide - the country is well-positioned. The country's strong healthcare system experienced clinical researchers, and the supportive government provides a solid foundation for growth in this area.

Market Restraints

There are certain limitations to oncology clinical trials in the Netherlands. One of the most significant challenges is the stringent standards regulating clinical studies. The regulatory procedure may be time-consuming and complicated, and failing to comply can result in fines. This may be difficult for certain firms, especially those unfamiliar with the Dutch regulatory structure. Competition is another challenge confronting oncology clinical trials in the Netherlands. Since nations compete to recruit clinical trials, the Netherlands may face competition from other countries that provide comparable benefits. Additionally, although the Netherlands government funds research and development, financing for clinical trials may be difficult to come by. Many organisations need substantial financial resources to perform clinical trials, and obtaining financing may be difficult.

Competitive Landscape

Key Players

  • Roche Holding AG
  • Pfizer Inc.
  • Novartis International AG
  • Merck & Co., Inc.
  • AstraZeneca plc
  • Eli Lilly and Company
  • Sanofi S.A.
  • Bristol Myers Squibb Company
  • Kiadis Pharma (NLD)
  • ISA Pharmaceuticals BV (NLD)

Notable Insights

  1. February 2023, The Netherlands Cancer Institute is doing research on a novel form of mesothelioma therapy. For individuals with BAP1 genetic alterations, researchers are investigating a unique combination of current drugs.
  2. September 2022, the new treatment, according to the researchers at the Netherlands Cancer Institute, utilizes a patient's own immune cells to attack cancer, and its therapy is comparable to another form of treatment that has shown to be very successful for blood malignancies, known as CAR-T therapy.
  3. April 2022, The Netherlands is investing 325 million euros ($351 million) in the development of preclinical cancer drugs. The Netherlands National Growth Fund intended to use the funds to establish specific competencies that would aid biotech in the development of cancer prospects.

Healthcare Policies and Regulatory Landscape

The Netherlands maintains two registries related to clinical trials. The Central Committee on Research Involving Human Subjects (CCMO) is a national registry that requires clinical trial data performed in the Netherlands or by a Dutch researcher to be posted. The summary findings must be submitted to the CCMO registry. Another registry that allows protocol registration is the National Trial Registry (NTR). It is a main registry recognized by the World Health Organization (WHO). NTR will have a new website starting on December 15, 2022. The NTR is administered by the CCMO, and once fully operational, the CCMO will reapply to the WHO for registration recognition.

The European Union Clinical Trial Information System (EU CTIS) became operational on January 31, 2022, and the Clinical Trials Regulation (Regulation (EU) No 536/2014) is currently in effect. EU CTIS will assist with protocol registration as well as results reporting for clinical trials performed in the EU/EEA.

1. Executive Summary
1.1 Disease Overview
1.2 Global Scenario
1.3 Country Overview
1.4 Healthcare Scenario in Country
1.5 Clinical Trials Regulation in Country
1.6 Recent Developments in the Country

2. Market Size and Forecasting
2.1 Market Size (With Excel and Methodology)
2.2 Market Segmentation (Check all Segments in Segmentation Section)

3. Market Dynamics
3.1 Market Drivers
3.2 Market Restraints

4. Competitive Landscape
4.1 Major Market Share
4.2 Key Company Profile (Check all Companies in the Summary Section)

4.2.1 Company
4.2.1.1 Overview
4.2.1.2 Product Applications and Services
4.2.1.3 Recent Developments
4.2.1.4 Partnerships Ecosystem
4.2.1.5 Financials (Based on Availability)

5. Reimbursement Scenario
5.1 Reimbursement Regulation

6. Methodology and Scope

Oncology Clinical Trials Market Segmentation

By Phase (Revenue, USD Billion):

  • Phase I
  • Phase II
  • Phase III
  • Phase IV

By Study Design Outlook (Revenue, USD Billion):

  • Epilepsy
  • Parkinson's Disease (PD)
  • Huntington's Disease
  • Stroke
  • Traumatic Brain Injury (TBI)
  • Amyotrophic Lateral Sclerosis (ALS)
  • Muscle regeneration
  • Others

By Indication Outlook  (Revenue, USD Billion):

  • Interventional
  • Observational
  • Expanded Access

Methodology for Database Creation

Our database offers a comprehensive list of healthcare centers, meticulously curated to provide detailed information on a wide range of specialties and services. It includes top-tier hospitals, clinics, and diagnostic facilities across 30 countries and 24 specialties, ensuring users can find the healthcare services they need.​

Additionally, we provide a comprehensive list of Key Opinion Leaders (KOLs) based on your requirements. Our curated list captures various crucial aspects of the KOLs, offering more than just general information. Whether you're looking to boost brand awareness, drive engagement, or launch a new product, our extensive list of KOLs ensures you have the right experts by your side. Covering 30 countries and 36 specialties, our database guarantees access to the best KOLs in the healthcare industry, supporting strategic decisions and enhancing your initiatives.

How Do We Get It?

Our database is created and maintained through a combination of secondary and primary research methodologies.

1. Secondary Research

With many years of experience in the healthcare field, we have our own rich proprietary data from various past projects. This historical data serves as the foundation for our database. Our continuous process of gathering data involves:

  • Analyzing historical proprietary data collected from multiple projects.
  • Regularly updating our existing data sets with new findings and trends.
  • Ensuring data consistency and accuracy through rigorous validation processes.

With extensive experience in the field, we have developed a proprietary GenAI-based technology that is uniquely tailored to our organization. This advanced technology enables us to scan a wide array of relevant information sources across the internet. Our data-gathering process includes:

  • Searching through academic conferences, published research, citations, and social media platforms
  • Collecting and compiling diverse data to build a comprehensive and detailed database
  • Continuously updating our database with new information to ensure its relevance and accuracy

2. Primary Research

To complement and validate our secondary data, we engage in primary research through local tie-ups and partnerships. This process involves:

  • Collaborating with local healthcare providers, hospitals, and clinics to gather real-time data.
  • Conducting surveys, interviews, and field studies to collect fresh data directly from the source.
  • Continuously refreshing our database to ensure that the information remains current and reliable.
  • Validating secondary data through cross-referencing with primary data to ensure accuracy and relevance.

Combining Secondary and Primary Research

By integrating both secondary and primary research methodologies, we ensure that our database is comprehensive, accurate, and up-to-date. The combined process involves:

  • Merging historical data from secondary research with real-time data from primary research.
  • Conducting thorough data validation and cleansing to remove inconsistencies and errors.
  • Organizing data into a structured format that is easily accessible and usable for various applications.
  • Continuously monitoring and updating the database to reflect the latest developments and trends in the healthcare field.

Through this meticulous process, we create a final database tailored to each region and domain within the healthcare industry. This approach ensures that our clients receive reliable and relevant data, empowering them to make informed decisions and drive innovation in their respective fields.

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Last updated on: 22 December 2023
Updated by: Ritu Baliya

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