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levofloxacin-based triple therapy

National Taiwan University Hospital · FDA-approved active Small molecule

Levofloxacin-based triple therapy combines a fluoroquinolone antibiotic with two other agents to eradicate Helicobacter pylori infection by inhibiting bacterial DNA gyrase and topoisomerase IV.

Levofloxacin-based triple therapy combines a fluoroquinolone antibiotic with two other agents to eradicate Helicobacter pylori infection by inhibiting bacterial DNA gyrase and topoisomerase IV. Used for Helicobacter pylori infection eradication in peptic ulcer disease, H. pylori-associated gastritis.

At a glance

Generic namelevofloxacin-based triple therapy
SponsorNational Taiwan University Hospital
Drug classFluoroquinolone antibiotic (in combination therapy)
TargetBacterial DNA gyrase and topoisomerase IV
ModalitySmall molecule
Therapeutic areaInfectious Disease / Gastroenterology
PhaseFDA-approved

Mechanism of action

Levofloxacin is a fluoroquinolone that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription in H. pylori. In triple therapy formulations, levofloxacin is combined with additional antimicrobial agents (typically amoxicillin and a proton pump inhibitor, or similar combinations) to achieve synergistic bacterial eradication and reduce antibiotic resistance. This combination approach targets H. pylori through multiple mechanisms simultaneously.

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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