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levofloxacin-based sequential therapy

National Taiwan University Hospital · FDA-approved active Small molecule

Levofloxacin-based sequential therapy uses a fluoroquinolone antibiotic in a multi-step treatment regimen to eradicate bacterial infections, particularly Helicobacter pylori in peptic ulcer disease.

Levofloxacin-based sequential therapy uses a fluoroquinolone antibiotic in a multi-step treatment regimen to eradicate bacterial infections, particularly Helicobacter pylori in peptic ulcer disease. Used for Helicobacter pylori eradication in peptic ulcer disease (as part of sequential therapy regimen).

At a glance

Generic namelevofloxacin-based sequential therapy
Also known asTakepron, Cravit, Flagyl, Amoxicillin
SponsorNational Taiwan University Hospital
Drug classFluoroquinolone antibiotic
TargetBacterial DNA gyrase; 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 sequential therapy protocols, levofloxacin is administered in a defined sequence with other antimicrobial agents (typically proton pump inhibitors and other antibiotics) to improve eradication rates of H. pylori and reduce antibiotic resistance compared to standard triple or dual therapy.

Approved indications

Common side effects

Key clinical trials

Primary sources

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