Drug intelligence / Profile preview

bedaquiline + delamanid + linezolid + levofloxacin + clofazimine

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Small Molecules
Administration
Oral
01

Overview

This is an investigational, all-oral combination regimen consisting of five drugs—bedaquiline, delamanid, linezolid, levofloxacin, and clofazimine—used for the treatment of multidrug-resistant tuberculosis (MDR-TB), including cases with additional resistance to fluoroquinolones or second-line injectables. Each component has a distinct mechanism of action targeting Mycobacterium tuberculosis. Bedaquiline inhibits mycobacterial ATP synthase; delamanid inhibits mycolic acid synthesis; linezolid inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit; levofloxacin is a fluoroquinolone that targets DNA gyrase and topoisomerase IV; and clofazimine binds to bacterial DNA and disrupts replication. This regimen aims to improve outcomes in MDR-TB patients by providing a potent oral alternative with reduced toxicity compared to traditional regimens. Clinical trials such as the DRAMATIC trial are evaluating its efficacy and optimal duration[1][6][7].

Other names
levofloxacin-Boston University-multidrug-resistant tuberculosisDRAMATIC Trial regimen5-drug MDR-TB regimen
02

Targets

Bacterial 50S ribosomal subunitATP SynthaseTopo IV (Bacterial Topoisomerase IV)AtpC (ATP synthase subunit epsilon)DNA gyrase

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