Drug intelligence / Profile preview

moxifloxacin + isoniazid + rifampin + pyrazinamide

Development stage
Phase 3
Modality
Small Molecules
Administration
Oral
01

Overview

This drug is a fixed-dose combination of four antibiotics—moxifloxacin, isoniazid, rifampin, and pyrazinamide—used in the treatment of active tuberculosis (TB). Each component has a distinct mechanism of action targeting *Mycobacterium tuberculosis*: - **Moxifloxacin** is a fluoroquinolone that inhibits bacterial DNA gyrase and topoisomerase IV, interfering with DNA replication. - **Isoniazid** inhibits mycolic acid synthesis in the mycobacterial cell wall. - **Rifampin** inhibits DNA-dependent RNA polymerase in susceptible bacteria. - **Pyrazinamide** disrupts membrane transport and energy production in *M. tuberculosis*. This combination regimen has been studied as an alternative to standard TB therapy to potentially shorten treatment duration or improve efficacy, especially for drug-susceptible pulmonary TB[1][4][6]. While combinations such as moxifloxacin plus rifampin plus pyrazinamide have shown promise in preclinical models[1][4], most clinical regimens substitute either moxifloxacin or isoniazid rather than using all four together routinely.

02

Targets

rpoB (DNA-directed RNA polymerase subunit beta)Aspartate decarboxylaseMycobacterium tuberculosis cell membraneInhARPSA (37/67 kDa laminin receptor)DNA gyraseRNAP (Bacterial dna-dependent RNA polymerase)Topo IV (Bacterial Topoisomerase IV)FAS-I (Mycobacterial fatty acid synthase I complex)

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