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Ciprofloxacin 0.3%

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

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

Ciprofloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription. Used for Bacterial conjunctivitis, Corneal ulcers, Other bacterial eye infections.

At a glance

Generic nameCiprofloxacin 0.3%
Also known asCETRAXAL OTICO®
SponsorIndiana University School of Medicine
Drug classFluoroquinolone antibiotic
TargetDNA gyrase, topoisomerase IV
ModalitySmall molecule
Therapeutic areaInfectious Disease / Ophthalmology
PhaseFDA-approved

Mechanism of action

Ciprofloxacin 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 leads to rapid bactericidal activity against a broad spectrum of gram-negative and gram-positive bacteria. 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

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