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Pretomanid in drug-resistant tuberculosis: a profile of its use

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Abstract

Pretomanid, a nitroimidazoxazine antimycobacterial agent, presents a valuable option for the treatment of adults with pulmonary extensively drug-resistant (XDR) tuberculosis (TB) or treatment-intolerant or nonresponsive multidrug-resistant (MDR)-TB when used as part of an all-oral combination regimen with bedaquiline and linezolid. In the pivotal phase III Nix-TB trial, a combination regimen of pretomanid, bedaquiline, and linezolid for 6 months had a high treatment success rate. Besides the demonstrated effectiveness, the pretomanid, bedaquiline, and linezolid combination has other benefits, including the convenience of oral administration, a relatively short treatment duration, and a relatively low potential for drug-drug interactions.

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Acknowledgements

The manuscript was reviewed by: A. D. Baughn, Department of Microbiology and Immunology, University of Minnesota Medical School, Minneapolis, MN, USA; C. L. Daley, Division of Mycobacterial and Respiratory Infections, Department of Medicine, National Jewish Health, Denver, CO, USA. During the peer review process, TB Alliance, the marketing-authorization holder of pretomanid, was also offered an opportunity to provide a scientific accuracy review of their data. Changes resulting from comments received were made on the basis of scientific and editorial merit.

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Correspondence to Matt Shirley.

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The preparation of this review was not supported by any external funding.

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M. Shirley is an employee of Adis International Ltd./Springer Nature, is responsible for the article content and declares no conflicts of interest.

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Enhanced material for this Adis Drug Q&A can be found at https://doi.org/10.6084/m9.figshare.12278645.

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Shirley, M. Pretomanid in drug-resistant tuberculosis: a profile of its use. Drugs Ther Perspect 36, 273–279 (2020). https://doi.org/10.1007/s40267-020-00743-9

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