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levofloxacin; metronidazole

Johnson & Johnson Pharmaceutical Research & Development, L.L.C. · FDA-approved active Small molecule

This combination uses levofloxacin (a fluoroquinolone that inhibits bacterial DNA gyrase and topoisomerase IV) and metronidazole (a nitroimidazole that damages bacterial DNA) to provide broad-spectrum anaerobic and aerobic bacterial coverage.

This combination uses levofloxacin (a fluoroquinolone that inhibits bacterial DNA gyrase and topoisomerase IV) and metronidazole (a nitroimidazole that damages bacterial DNA) to provide broad-spectrum anaerobic and aerobic bacterial coverage. Used for Mixed aerobic and anaerobic bacterial infections, Intra-abdominal infections, Pelvic inflammatory disease.

At a glance

Generic namelevofloxacin; metronidazole
SponsorJohnson & Johnson Pharmaceutical Research & Development, L.L.C.
Drug classFluoroquinolone + Nitroimidazole combination antibiotic
TargetBacterial DNA gyrase, topoisomerase IV (levofloxacin); bacterial DNA (metronidazole)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Levofloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription in gram-negative and gram-positive bacteria. Metronidazole is a nitroimidazole antibiotic that is reduced to reactive intermediates inside anaerobic bacteria, causing DNA strand breaks and cell death. Together, they provide synergistic coverage against both aerobic and anaerobic pathogens, commonly used in mixed infections.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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