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group-B : Levofloxacin triple therapy

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh · FDA-approved active Small molecule

Levofloxacin triple therapy combines a fluoroquinolone antibiotic with two additional agents to inhibit bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription in susceptible microorganisms.

Levofloxacin triple therapy combines a fluoroquinolone antibiotic with two additional agents to inhibit bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription in susceptible microorganisms. Used for Helicobacter pylori eradication in peptic ulcer disease, Resistant bacterial infections.

At a glance

Generic namegroup-B : Levofloxacin triple therapy
SponsorBangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Drug classFluoroquinolone antibiotic combination therapy
TargetBacterial DNA gyrase, topoisomerase IV
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Levofloxacin is a fluoroquinolone that inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication and repair. The triple therapy formulation combines levofloxacin with additional antimicrobial agents (typically clarithromycin and amoxicillin or similar) to provide synergistic activity against resistant pathogens, particularly for eradication of Helicobacter pylori and other resistant 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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