India's oncology clinical trials market is projected to grow from $230.1 Mn in 2022 to $441.8 Mn by 2030, registering a CAGR of 8.5% during the forecast period of 2022-30. The market will be driven by the rising prevalence of Oncological disorders, the availability of a large patient pool with various genetic profiles, and low-cost clinical trials. The market is segmented by phase, by study design & by indication. Some of the major players include Pfizer Inc., Sun Pharmaceutical Industries Ltd., Cadila Healthcare Ltd. & Cipla Ltd.
The India oncology clinical trials market is projected to grow from $230.1 Mn in 2022 to $441.8 Mn by 2030, registering a CAGR of 8.5% during the forecast period of 2022-30. According to the Indian Council of Medical Research's (ICMR) National Cancer Registry Project, the anticipated incidence of cancer cases in India across different states and union territories in 2020 was 1.39 Mn rising to 1.42 Mn in 2021 and 1.46 Mn in 2022 and are expected to double by 2040. The five most frequent malignancies in India are lung, oral, cervical, breast, and stomach cancer. In India, one in every nine persons will acquire cancer over their lifetime. Lung and breast cancers were the most common cancer locations in men and women, respectively.
Clinical trials in India are still 60% cheaper than in the United States. India has 1,762 world-class hospitals as trial locations and 4,216 ICH-GCP-qualified investigators. In recent years, India's oncology clinical trials industry has grown significantly. With a big and diversified patient population, a well-established healthcare system, and relatively inexpensive rates when compared to developed countries, India has become an appealing venue for pharmaceutical firms seeking to perform oncology clinical trials.
Various hospitals and research institutes in India are involved in oncology clinical trials for example;
In November 2022, An ultra-low dosage of the immunotherapy medicine nivolumab (Opdivo) was shown to help persons with advanced head and neck cancer live much longer lives in Indian research. Additionally, since the dosage is 6% of what is generally used in the United States and Europe, it may be less expensive.
Market Growth Drivers
The Network of Oncology Clinical Trials in India (NOCI) is a National Biopharma Mission programme backed by the Biotechnology Industry Research Assistance Council (BIRAC). This project's goal is to improve the capacity to undertake industry-sponsored clinical studies of cancer medicines and biosimilars with the ultimate goal to boost and accelerate the indigenous development of novel anti-cancer medicines.
The number of clinical trials undertaken in India has increased significantly, notably in oncology. The availability of a large patient pool with various genetic profiles is crucial for assessing the safety and effectiveness of novel cancer medicines. Moreover, India has a well-established medical infrastructure, including a robust network of hospitals and research institutes, allowing for easy recruitment and supervision of clinical trial participants. Another reason driving the rise of cancer clinical trials in India is the availability of trained clinical research workers at a cheaper cost than in other nations. As a result, India has become an appealing site for sponsors seeking to conduct cost-effective clinical studies without sacrificing quality.
Market Restraints
There are other constraints to consider as well. Regulatory compliance is one of the most significant barriers to the expansion of cancer clinical trials in India. Regulatory authorities have expressed concerns in recent years regarding the safety of clinical trial participants and the ethical standards of certain trials. This has led to greater scrutiny and more severe rules, which may lead to delays in research approvals and higher expenses.
Another issue confronting cancer clinical trials in India is a lack of clinical trial knowledge and comprehension among patients and healthcare professionals. This may make it more challenging to recruit qualified volunteers and have an influence on the quality of data collected by the research.
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
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