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Pretomanid: The latest USFDA-approved anti-tuberculosis drug
1Department of Pharmacology, Burdwan Medical College, Burdwan.
Abstract:
Pretomanid is a nitroimidazooxazine drug which inhibits synthesis of mycolic acid. This leads to defective cell wall formation, ultimately causing bacterial cell death. It is active against both replicating and non-replicating M. tuberculosis. Following promising result in a phase III trial, pretomanid was approved by United States Food and Drug Administration in August 2019. This orally active drug has been approved as part of a combination regimen of bedaquiline, pretomanid and linezolid (BPaL regimen) to treat adults with pulmonary extensive drug resistant tuberculosis (TB) or treatment-intolerant or non-responsive multidrug resistant TB. Peripheral neuropathy and increased liver enzymes are some of the reported adverse events associated with pretomanid. However, more studies are required to confirm the role of pretomanid in paediatric, geriatric and HIV co-infection cases.
Insights
Pretomanid, a novel drug, effectively treats multidrug-resistant tuberculosis by disrupting bacterial cell walls. Approved in 2019, it shows promise in combination therapy for extensive drug-resistant tuberculosis.
Area of Science:
- Pharmacology and Microbiology
- Drug Discovery and Development
Background:
- Tuberculosis (TB) remains a significant global health challenge, particularly drug-resistant strains.
- Mycolic acid synthesis is crucial for Mycobacterium tuberculosis cell wall integrity.
- Limited treatment options exist for extensively drug-resistant tuberculosis (XDR-TB) and multidrug-resistant tuberculosis (MDR-TB).
Purpose of the Study:
- To introduce pretomanid, a novel nitroimidazooxazine drug.
- To highlight its mechanism of action against Mycobacterium tuberculosis.
- To discuss its recent approval and therapeutic role in resistant TB.
Main Methods:
- Pretomanid targets mycolic acid synthesis, a key component of the mycobacterial cell wall.
- Its efficacy was demonstrated in a Phase III clinical trial.
- Approved as part of the bedaquiline, pretomanid, and linezolid (BPaL) regimen.
Main Results:
- Pretomanid inhibits mycolic acid synthesis, leading to bacterial cell death.
- The drug is active against both replicating and non-replicating Mycobacterium tuberculosis.
- The BPaL regimen showed promising results in treating adults with XDR-TB or treatment-intolerant/non-responsive MDR-TB.
Conclusions:
- Pretomanid represents a significant advancement in the treatment of drug-resistant tuberculosis.
- Further research is needed to evaluate its use in pediatric, geriatric, and HIV co-infected populations.
- The BPaL regimen offers a new therapeutic option for complex TB cases.
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