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Updated: Jul 16, 2026

A High-throughput Compatible Assay to Evaluate Drug Efficacy against Macrophage Passaged Mycobacterium tuberculosis
Published on: March 24, 2017
New tuberculosis drugs in development
1Complications and Co-Infections Research Branch, Therapeutics Research Program, Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-7624, USA. BLaughon@niaid.nih.gov
No new tuberculosis (TB) drug classes have emerged in 50 years, despite millions dying annually. Global efforts focus on new chemical entities and control strategies due to rising drug resistance and industry disinterest.
Area of Science:
- Infectious Diseases
- Drug Development
- Global Health
Background:
- Tuberculosis (TB) remains a critical global health emergency, causing millions of deaths and infections yearly, particularly in developing nations.
- The TB epidemic is accelerating in Africa and Asia, exacerbated by the HIV epidemic and increasing resistance to standard drugs like isoniazid and rifampicin.
- The pharmaceutical industry's withdrawal from TB drug development, citing market non-profitability, has created a critical gap in addressing this persistent disease.
Purpose of the Study:
- To highlight the urgent need for novel drug classes to combat tuberculosis.
- To underscore the challenges posed by multidrug-resistant and extensively drug-resistant TB strains.
- To emphasize the shift towards public sector and research-driven initiatives in TB drug discovery.
Main Methods:
- Review of historical TB drug development trends and current treatment landscape.
- Analysis of factors contributing to the rise of drug-resistant tuberculosis.
- Examination of the role of public health initiatives, research funding, and partnerships in advancing TB control.
Main Results:
- No new classes of TB drugs have been introduced in the last 50 years.
- Emerging resistance patterns are rendering current antibiotics ineffective against certain mycobacteria strains.
- Public and research sectors are actively developing new chemical entities and control strategies, but advanced development and clinical trials remain under-resourced.
Conclusions:
- There is a critical unmet need for new tuberculosis drugs due to widespread resistance and lack of industry investment.
- Continued collaboration between public sectors, researchers, funding agencies, and philanthropic donors is essential for TB drug development.
- Addressing advanced preclinical and Phase III clinical trial gaps is crucial for bringing new TB therapies to patients.
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