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Ofloxacin 0.3%

Indiana University School of Medicine · FDA-approved active Small molecule

Ofloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription.

Ofloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription. Used for Bacterial conjunctivitis, Bacterial corneal ulcers, Ocular infections caused by susceptible gram-positive and gram-negative bacteria.

At a glance

Generic nameOfloxacin 0.3%
SponsorIndiana University School of Medicine
Drug classFluoroquinolone antibiotic
TargetDNA gyrase, Topoisomerase IV
ModalitySmall molecule
Therapeutic areaInfectious Disease / Ophthalmology
PhaseFDA-approved

Mechanism of action

Ofloxacin works by binding to and inhibiting bacterial DNA gyrase (in gram-negative bacteria) and topoisomerase IV (in gram-positive bacteria), enzymes essential for DNA replication and repair. This leads to disruption of bacterial DNA synthesis, cell death, and bactericidal activity. The 0.3% ophthalmic formulation is used topically on the eye to treat bacterial infections.

Approved indications

Common side effects

Key clinical trials

Primary sources

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