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Safety and Efficacy of Delamanid in the Treatment of Multidrug-Resistant Tuberculosis (MDR-TB)
Author(s) -
Stephen K. Field
Publication year - 2013
Publication title -
clinical medicine insights therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.205
H-Index - 9
ISSN - 1179-559X
DOI - 10.4137/cmt.s11675
Subject(s) - medicine , bedaquiline , tuberculosis , multiple drug resistance , isoniazid , antibiotics , drug resistance , intensive care medicine , clinical trial , incidence (geometry) , mycobacterium tuberculosis , microbiology and biotechnology , pathology , biology , physics , optics
Globally, the incidence of tuberculosis (TB) is declining but the proportion of drug-resistant cases has increased. Strains resistant to both isoniazid and rifampin, and possibly other antibiotics, called multidrug-resistant (MDR), are particularly difficult to treat. Poorer outcomes, including increased mortality, occur in patients infected with MDR strains and the costs associated with treatment of MDR-TB are substantially greater. The recent recognition of MDR-TB and strains with more complex resistance patterns has stimulated the development of new TB medications including fluoroquinolones, oxazolidinones, diarylquinolines, nitroimidazopyrans, ethylenediamines, and benzothiazinones. Bedaquiline, a diarylquinoline, was approved for the treatment of MDR-TB in 2012. Addition of delamanid to WHO-approved treatment improved outcomes for MDR-TB and for extensively drug-resistant TB in a large randomized, controlled phase II clinical trial and is undergoing evaluation in a large international phase III study. This review will focus on MDR-TB and the role of delamanid in its treatment.

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