The Philippines oncology clinical trials market is projected to grow from $27.8 Mn in 2022 to $44.4 Mn by 2030, registering a CAGR of 6% during the forecast period of 2022-30. The market will be driven by the growing cancer burden, favorable regulatory environment, and cheaper costs. The market is segmented by phase, by study design & by indication. Some of the major players include Pfizer Inc., Novartis International AG & AstraZeneca plc.
The Philippines oncology clinical trials market is projected to grow from $27.8 Mn in 2022 to $44.4 Mn by 2030, registering a CAGR of 6% during the forecast period of 2022-30. Clinical trials are governed in the Philippines by the Department of Health (DOH) and the Food and Drug Administration (FDA) (FDA). The FDA is a DOH agency in charge of guaranteeing the safety, effectiveness, and quality of food, medicines, cosmetics, and medical devices. According to 2019 projections, the Philippine government supports slightly more than 40% of overall cancer costs, with out-of-pocket payments and private insurance covering the rest (Philippines Statistical Agency, 2020). Cancer is the Philippines' second biggest cause of mortality. Breast, lung, colorectal, liver, and prostate cancers are the most prevalent. Cancer is one of the main causes of mortality in the Philippines, of over 110 Mn people. Cancer was responsible for approximately 150,000 new diagnoses and over 90,000 fatalities in 2020 alone.
Because of its vast population and developing clinical research infrastructure, the Philippines is emerging as a destination for oncology clinical trials. Participation in oncology clinical trials in the nation has increased in recent years, with a focus on diseases such as breast cancer, lung cancer, and leukaemia. There has been a rise in the number of local and foreign pharmaceutical firms and research institutions conducting trials in the country, making it an important site for oncology clinical trials in Southeast Asia. The nation has the potential to become an even more prominent participant in the global cancer research landscape as it continues to invest in clinical research infrastructure and raise public awareness about clinical trials.
Market Growth Drivers
Recognizing the growing cancer burden, the government has recently increased its cancer-fighting efforts, as evidenced by the formation of the National Cancer Control Committee (NCCC), which is comprised of multi-stakeholder representatives from the government, patient organizations, and medical providers. The National Cancer Prevention and Control Action Plan (NCPCAP) 2015-2020 was designed and released by this group. The introduction of the Z-benefit package, as well as the recommendation that the DOH conduct cervical cancer screening and HPV vaccination programs, are key components of the strategy. The proposed National Integrated Cancer Control Strategy Plan for 2021-2030 is now being reviewed in order to properly overcome obstacles in transition and implementation. The growing cancer burden, a huge patient pool, competent healthcare workers, and government support are all key factors for oncology clinical trials in the Philippines. The favorable regulatory environment and cheaper costs also attract multinational corporations. The pandemic's trend toward virtual and decentralized testing might fuel additional expansion.
Market Restraints
In a 2020 WPRO assessment, the Philippines placed last in policy, planning, and care delivery, and ninth out of ten nations in health system governance. There are also several other barriers to the expansion of oncology clinical trials in the Philippines. One of the most significant barriers is the general public's lack of knowledge and comprehension of clinical trials. Many Filipinos are unfamiliar with clinical trials, and there is a need to raise awareness and educate people about the advantages of clinical research. Another barrier is the regulatory framework in the Philippines for clinical studies. Although the government has made steps to shorten the regulatory procedure for clinical trials, acquiring the requisite clearances and licenses for clinical research still involves considerable complexity. This might increase the time and expense of performing clinical studies in the nation.
Key Players
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
By Phase (Revenue, USD Billion):
By Study Design Outlook (Revenue, USD Billion):
By Indication Outlook (Revenue, USD Billion):
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:
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:
2. Primary Research
To complement and validate our secondary data, we engage in primary research through local tie-ups and partnerships. This process involves:
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:
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.
We value your inquiry and offer free customization with every report to fulfil your exact research needs.