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Moxifloxacin 0.5% ophthalmic solution

Johns Hopkins University · FDA-approved active Small molecule

Moxifloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and causing bacterial cell death.

Moxifloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and causing bacterial cell death. Used for Bacterial conjunctivitis, Bacterial keratitis, Bacterial corneal ulcer.

At a glance

Generic nameMoxifloxacin 0.5% ophthalmic solution
Also known asVigamox
SponsorJohns Hopkins University
Drug classFluoroquinolone antibiotic
TargetBacterial DNA gyrase and topoisomerase IV
ModalitySmall molecule
Therapeutic areaOphthalmology / Infectious Disease
PhaseFDA-approved

Mechanism of action

As a broad-spectrum fluoroquinolone, moxifloxacin 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 transcription. This dual mechanism results in rapid bactericidal activity against a wide range of gram-positive and gram-negative ocular pathogens. The ophthalmic formulation delivers high local concentrations to the eye while minimizing systemic exposure.

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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