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  • Tuberculosis Epidemiology Study

    ID: MRFR/59
    200 Pages
    MRFR Team
    June 2025
    $ 4950
    $ 5950
    $ 7950

    Epidemiology Study - Overview

    Tuberculosis (TB) Study Objective:

    To determine the prevalence and incidence of Tuberculosis (TB) among individuals in a defined population. This objective outlines the primary aim of the study, which is to establish the frequency of Tuberculosis (TB) within a specific age group and geographic area, while also seeking to understand potential factors contributing to its development. Moreover, the report is having geographic coverage including North America, Europe and rest of the world however customisation can be made in the geographic coverage.

    Tuberculosis (TB) Study USP:

    • This epidemiological study on Tuberculosis (TB) stands out due to its comprehensive approach in establishing precise prevalence rates, identifying novel risk factors, and exploring geographical variations in a diverse population.
    • By integrating advanced imaging techniques with robust statistical analyses, the study aims to provide actionable insights to identify treatment opportunities, target population, and an overview on public health initiatives aimed at mitigating the impact of Tuberculosis (TB) related health problems.
    • Through meticulous data collection and rigorous methodology, the study not only contributes to the scientific understanding of Tuberculosis (TB) but also serves as a foundation for future research events and healthcare policymaking in addressing this increasing Tuberculosis (TB) cases.

    Tuberculosis (TB) related Study Overview:

    The study Defines Tuberculosis (TB) as an advanced form of disease. The significance of studying Tuberculosis (TB) epidemiology is due to its increasing prevalence in different age populations.

    Tuberculosis (TB) Study Design:

    Population: The target population and the sampling method (e.g., random sampling from healthcare registries or population databases)

    Data Collection: Detail methods for identifying Tuberculosis (TB) cases (e.g., clinical examination, imaging studies) and demographic data (age, sex, ethnicity).

    Tuberculosis (TB) Epidemiological Parameters:

    Prevalence: Prevalence rates considered per 1,000 or 10,000 population.

    Incidence: Determine annual incidence rates per 1,000 person-years.

    Risk Factors: Analyse associations between Tuberculosis (TB) and potential risk factors (e.g., age, smoking, genetics).

    Geographical Variations: Compare prevalence or incidence rates across different regions or countries.

     

                                            

     

    Tuberculosis (TB) study summary:

    Tuberculosis (TB) study summarizes the prevalence, incidence, possible risk factors, and geographic variations of the Tuberculosis (TB) worldwide.

    Tuberculosis (TB) Disease overview:

    Tuberculosis (TB) is potentially serious infectious disease caused by bacterium Mycobacterium Tuberculosis. It primarily affects lungs (pulmonary Tb) but can also affect other parts of body (extrapulmonary TB). Mode of transmission is airborne, spread through droplets when an infected person coughs, sneezes or talks. Symptoms include persistent cough for more than 2 weeks, coughing up blood, chest pain, fatigue, fever, weight loss, loss of appetite.

    As of 2023, tuberculosis (TB) remains major global health concern, world health organisation reports that approximately 10.8 million people worldwide fell ill with TB in 2023, with incidence rates of 134 cases per 100,000 population. In 2023, the majority of tuberculosis cases were reported in the WHO South-East Asia Region (45%), followed by the African Region (24%) and the Western Pacific Region (17%). Smaller proportions were observed in the Eastern Mediterranean (8.6%), the Americas (3.2%), and the European Region (2.1%).

    Various treatment options available in the market include First-Line Therapies, Second-Line Therapies, Multidrug-Resistant Therapies, Extensively Drug-Resistant Therapies and certain drugs used in the treatment are as follows Quinolones, Rifamycins, Nitroimidazoles, Macrolides, Aminoglycosides. Key market players manufacturing therapeutics for the treatment of tuberculosis patients include Mylan, Pfizer, GlaxoSmithKline, Cipla, Merck Co, Boehringer Ingelheim, AstraZeneca, Abbott Laboratories, Lupin, Teva Pharmaceutical Industries, Alkermes, Novartis, Johnson Johnson, Sanofi, Otsuka Pharmaceutical.

    May 2025, Serum Institute of India and Mylab have launched a point-of-care skin test called Cy-TB for detecting latent tuberculosis infections (LTBI). This test is priced 50–70% lower than existing alternatives, costing around ₹1,200–1,500, making it more accessible. It combines the simplicity of skin tests with the accuracy of interferon gamma release assays (IGRA), which are typically more expensive (₹3,000–6,000). The test has been included in India’s National Tuberculosis Elimination Programme (NTEP) via the Ni-kshay platform and is expected to play a key role in India’s goal to eliminate TB by 2025. The companies plan to supply the test to both the government and private sector and claim that no other company is likely to launch a similar product in the next 3–4 years due to the extensive clinical validation required.

    Tuberculosis (TB) Demographic and Environmental Risk Factors:

    Age and Sex:  according to WHO, In 2023, tuberculosis affected individuals across all age groups and sexes, but the burden was highest among adult men aged 15 years and older, accounting for an estimated 6.0 million cases—about 55% of the global total. Adult women in the same age group represented 33% of cases, with approximately 3.6 million infections. Children aged 0–14 years made up 12% of the total, with an estimated 1.25 million cases. The highest number of TB cases in most regions occurs among adults aged 25–54 years, particularly in the 25–34, 35–44, or 45–54 age groups. However, the WHO Western Pacific Region is an exception, where the largest number of cases is found in individuals aged 65 years and older. Newly diagnosed and reported cases were 75% of the estimated global TB cases identified in 2023. Varied incidence based on sex and age was: 76% for adult men, 80% for adult women, and only 55% for children. Alarmingly, among children under 5 years old, just 48% of TB cases were notified.

    Ethnicity: According to the centers for disease control and prevention (CDC) In 2023, a total of 1,697 non-Hispanic Black or African American individuals were reported with TB in the United States, representing 17.6% of all nationally reported TB cases. 40% of TB cases among U.S.-born individuals occurred in non-Hispanic Black population, with rate eight times higher than that among non-Hispanic whites. Additionally, the prevalence of latent TB infection (LTBI) among U.S.-born individuals has been significantly higher in non-Hispanic Blacks (5.7%) compared to Mexican Americans (2.5%) and non-Hispanic whites (1.1%).

    Risk Factors causing Tuberculosis (TB): TB is leading cause of death among people with HIV; it weakens immune system making it easier for mycobacterium tuberculosis to cause the disease. Malnourished individuals are about 3 times more likely to develop TB, tobacco smoking, diabetes also triggers risk of developing TB, close contact with active TB patients, air pollution are some the major factors which can cause TB.

    Tuberculosis (TB) Market Scope:

    Drivers: Tuberculosis is a bacterial infection affecting mainly the lungs even though it can as well spread to other organs. It is one of the most serious public health problems to date. Records estimate that there are 10 million new cases and 1.5 million deaths a year being reported worldwide. The increase in the prevalence of this infection is one of the major drivers of the Tuberculosis Therapeutics Market Industry. Increased population, urbanization, poverty, malnutrition, and weakened immune systems factors are aiding to increase the occurrence of this infection.

    Another factor driving the Tuberculosis Therapeutics Market Industry is the development of new and improved drugs. The treatment of tuberculosis by traditional methods is quite complex and may take time. Additionally, existing treatments may have adverse side effects. Therefore, there is a need for better treatment methods including more convenient and effective treatments. To meet the growing demand, many companies working in the pharmaceutical field invest heavily in research and development.

    Government initiatives and funding play a crucial role in supporting the Tuberculosis Therapeutics Market Industry. Governments worldwide recognize the importance of combating TB and have implemented various programs and policies to improve prevention, diagnosis, and treatment.

    Restraints: High burden in low-income countries, Drug Resistance and complexity of the treatment, lack of awareness, diagnostic gaps, long treatment duration, regulatory barriers, are some of the risk factors which can contribute to hinder the growth of the market involved in manufacturing the therapeutics for the treatment of Tuberculosis (TB).

    Epidemiology Study - Table of Content

    TOC (TAB 1) Market Introduction

    • Disease Overview
    • Causes and Risk Factors
    • Disease Mortality Rate

    Market Scope

    • Qualitative Analysis
      • Drivers
      • Restraints
      • Diseases Analysis, By Age Group
    • Quantitative Analysis
      • Number of Patients (2019-2032)- By Region
        • Global
        • North America
        • Europe
        • Asia-Pacific
        • ROW
      • Incidence Rate- By Region
        • Global
        • North America
        • Europe
        • Asia-Pacific
        • ROW
      • Prevalence Rate- By Region
        • Global
        • North America
        • Europe
        • Asia-Pacific
        • ROW

    LIST OF TABLES TABLE 1: GLOBAL NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 TABLE 2: GLOBAL PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 3: GLOBAL INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 4: NORTH AMERICA NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 TABLE 5: NORTH AMERICA PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 6: NORTH AMERICA INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 7: EUROPE NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 TABLE 8: EUROPE PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 9: EUROPE INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 10: AISA-PACIFIC NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 TABLE 11: AISA-PACIFIC PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 12: AISA-PACIFIC INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 13: ROW NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 TABLE 14: ROW PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 TABLE 15: ROW INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 LIST OF FIGURES FIG 1: GLOBAL NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 FIG 2: GLOBAL PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 3: GLOBAL INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 4: NORTH AMERICA NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 FIG 5: NORTH AMERICA PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 6: NORTH AMERICA INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 7: EUROPE NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 FIG 8: EUROPE PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 9: EUROPE INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 10: AISA-PACIFIC NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 FIG 11: AISA-PACIFIC PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 12: AISA-PACIFIC INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 13: ROW NUMBER OF PATIENTS FOR TUBERCULOSIS (TB) FROM 2019-2032 FIG 14: ROW PREVALENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023 FIG 15: ROW INCIDENCE RATE FOR TUBERCULOSIS (TB) FROM 2019-2023  

    Pricing Analysis - Overview

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    Regulatory Landscape - Overview

    Overview for Regulatory Landscape (based on available reports).

    mRNA Vaccines And Therapeutics Regulatory Landscape: Product Overview mRNA vaccines and therapeutics are class of medical treatments that utilize synthetic messenger RNA (mRNA) to instruct the body’s cells to produce specific proteins. In the case of vaccines, these proteins mimic parts of a virus or pathogen, making the immune system to recognize and respond to future infections. For therapeutics, the mRNA directs cells to produce Specific proteins, which help to treat or manage diseases. mRNA Vaccines And Therapeutics Applications: mRNA vaccines offer rapid development and broad protection against various infectious diseases such as influenza, RSV, Zika, rabies, Ebola, and COVID-19 variants. They also support innovative delivery systems that enhance mucosal immunity, making them effective tool in modern disease prevention. One of the most promising uses of mRNA technology is in oncology. Personalized cancer vaccines are being developed to encode tumor-specific antigens, enabling the immune system to recognize and attack cancer cells. mRNA is showing promise in treating rare inherited diseases such as methylmalonic acidemia and glycogen storage disorders. These conditions often lack effective treatments, and mRNA offers a less invasive and more adaptable alternative to traditional gene therapy. Researchers are investigating how mRNA can be used to modulate immune responses in autoimmune diseases like multiple sclerosis and rheumatoid arthritis. By fine-tuning immune activity, mRNA could help reduce inflammation and prevent immune attacks on healthy tissue. mRNA Vaccines And Therapeutics Product Development steps: Figure: overview of FDA mRNA Vaccines and Therapeutics Approval and Development Process mRNA Vaccines And Therapeutics Market Size Overview: mRNA Vaccines and Therapeutics Market Size was estimated at 6.06 (USD Billion) in 2023. The mRNA Vaccines and Therapeutics Market Industry is expected to grow from 7.23 (USD Billion) in 2024 to 50.0 (USD Billion) by 2035. The mRNA Vaccines and Therapeutics Market CAGR (growth rate) is expected to be around 19.22% during the forecast period (2025-2035). mRNA Vaccines And Therapeutics Regulatory Landscape: There are several key regulatory agencies who oversee the approval and monitoring of mRNA Vaccines And Therapeutics to ensure their safety, efficacy, and quality. Regulatory agencies Regulatory Ministry Federal Food and Drug Administration United States: Department of Health and Human Services (HHS) The Medicines and Healthcare products Regulatory Agency United Kingdom: The Medicines and Healthcare products Regulatory Agency (MHRA) under the Department of Health and Social Care (DHSC) Central Drug Standard Control Organization India: The Ministry of Health and Family Welfare South African Health Products Regulatory Authority (SAHPRA) National Department of Health. Pharmaceuticals and Medical Devices Agency (PMDA) Japan: Ministry of Health, Labour and Welfare. National Medical Products Administration (NMPA) China: The Ministry of Health Health Sciences Authority Singapore: The Ministry of Health European Medicine Agency European union Brazilian Health Regulatory Agency (Anvisa) Ministry of Health, part of the Brazilian National Health System (SUS) mRNA Vaccines And Therapeutics Guidelines: mRNA-based therapies are emerging as a transformative approach for treating a wide range of diseases that are resistant to conventional treatments, including infectious diseases, metabolic genetic disorders, cancer, cardiovascular, and cerebrovascular conditions. These therapies offer several advantages, such as high efficacy, minimal side effects, and ease of production. The success of mRNA vaccines during the COVID-19 pandemic, particularly BNT162b2 by Pfizer-BioNTech and mRNA-1273 by Moderna, demonstrated the potential of this technology. These vaccines showed approximately 90% effectiveness in preventing infection in fully vaccinated individuals and around 80% in those partially vaccinated. mRNA Vaccines And Therapeutics Classification of the Product: mRNA Vaccines And Therapeutics Regulatory Process Overview, By Country: mRNA products are classified as biologics by the U.S. Food and Drug Administration (FDA), The Center for Biologics Evaluation and Research (CBER) under Food and Drug Administration (FDA) is responsible for the regulation of all the biologics including mRNA vaccines and therapeutics and make sure ...

    Regulatory Landscape - Table of Content

    Clinical Trial Analysis - Overview

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