Antimicrobial Agents and Chemotherapy · 2022 · 48 citations · 23 references
MedicineMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryMolecular PharmacologyAntibacterial AgentsMacrophage PharmacologyPulmonary TuberculosisTuberculosis CareTuberculosis PharmacotherapyDrug Candidate OptimizationMycobacterium Tuberculosis InfectionMycobacterium Tuberculosis PathogenesisTuberculosis Drug DevelopmentTuberculosis Drug Resistance
] = 0.07 μM), is active against extracellular bacteria in cholesterol-containing culture medium, and exhibits no cross-resistance with known antitubercular drugs. In addition, it has shown efficacy in different mouse models of tuberculosis (TB) and has an adequate safety profile in two preclinical species. These features indicate a compound with a novel mode of action, although still not fully defined, that is effective against both multidrug-resistant (MDR) or extensively drug-resistant (XDR) and drug-sensitive (DS) M. tuberculosis with the potential to shorten the duration of treatment in novel combination drug regimens. (This study has been registered at ClinicalTrials.gov under identifier NCT04472897).
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Global tuberculosis report (2014)
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Discovery of Q203, a potent clinical candidate for the treatment of tuberculosis
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Ipr1 gene mediates innate immunity to tuberculosis
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