The Tanzania Neurology Clinical Trials market is projected to grow from $2.09 Mn in 2022 to $3.44 Mn by 2030, registering a CAGR of 6.4% during the forecast period of 2022 - 2030. The market will be driven by investment in infrastructure, resources, and training for healthcare professionals, as well as collaboration between local and international stakeholders. The market is segmented by phase, by study design & by indication. Some of the major players include Novartis AG, Sanofi S.A., AstraZeneca & GlaxoSmithKline.
The Tanzania Neurology Clinical Trials market is projected to grow from $2.09 Mn in 2022 to $3.44 Mn by 2030, registering a CAGR of 6.4% during the forecast period of 2022 - 2030. Tanzania's population also has among the world's lowest rates of access to health personnel. Approximately 60% of Tanzania's healthcare facilities are government-run, with the remainder being faith-based or private. As Tanzania advances towards universal healthcare, the government allotted $387.9 million for the health sector in 2020/2021, of which $155.5 million would be spent on development projects to assist the government in implementing its health-improving efforts. According to the World Health Organization (WHO), neurological illnesses account for around 10% of the country's overall disease burden. Tanzania performed one of the few known population-based stroke incidence studies from SSA and discovered an age-standardized incidence rate of up to 316 per 100,000 people.
Clinical trials are an essential part of medical research since they are used to evaluate the safety and efficacy of new drugs, medical equipment, or treatments. Clinical trials are conducted to determine that innovative therapies or drugs are safe, effective, and appropriate for use in patient care. Neurology clinical trials, in particular, focus on treatments for neurological ailments such as Alzheimer's disease, multiple sclerosis, Parkinson's disease, stroke, and others. In Tanzania, neurology clinical trials are still very restricted in comparison to other countries, and the number of active studies in this sector is minimal. In recent years, however, there has been some success, with a few clinical trials in Tanzania evaluating novel treatments and therapies for neurological illnesses. There are several hospitals supportive of clinical trials such as Muhimbili National Hospital, Kilimanjaro Christian Medical Centre, Ifakara Health Institute, Bugando Medical Centre and others.
Market Growth Drivers
The high prevalence of neurological illnesses in Tanzania, including epilepsy, stroke, and neuro-infections, is one of the key drivers of growth. This has resulted in an urgent need for novel treatments and therapies, as well as improved access to current ones. Another driver of expansion is the growing interest in doing clinical research in Tanzania from both local and international partners. Tanzania has been recognised as a viable place for undertaking this sort of study due to a rising realisation of the need to create novel treatments and therapies that are especially suited to the requirements of patients in low-resource settings.
Market Restraints
There are also various constraints impeding the expansion of neurology clinical trials in Tanzania. One of the most significant problems is the country's poor infrastructure and resources for performing clinical research, especially in rural regions. This has resulted in a concentration of clinical studies in cities, which may restrict the generalizability of the findings to the general population. Another challenge is a lack of skilled healthcare personnel, notably neurologists and other experts required to conduct and monitor clinical studies. As a result, there is a greater dependence on overseas partners, which might provide extra obstacles in terms of coordination, communication, and cultural differences.
Key Players
The Tanzania Medicines and Medical Devices Authority (TMDA) and the Tanzania Commission for Science and Technology govern and supervise clinical research in Tanzania (COSTECH). In Tanzania, the TMDA is the regulatory body in charge of clinical trial authorization, monitoring, and inspections. In line with the TMMDAct and the CT-Regs, the TMDA gives approval for clinical trials to be undertaken in the nation.
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):
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