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Moxifloxacin (Topical)
Moxifloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription in susceptible microorganisms.
Moxifloxacin is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, preventing DNA replication and transcription in susceptible microorganisms. Used for Bacterial conjunctivitis, Bacterial corneal ulcer, Post-operative ocular infection prophylaxis.
At a glance
| Generic name | Moxifloxacin (Topical) |
|---|---|
| Sponsor | University of California, San Francisco |
| Drug class | Fluoroquinolone antibiotic |
| Target | Bacterial DNA gyrase and topoisomerase IV |
| Modality | Small molecule |
| Therapeutic area | Infectious Disease / Ophthalmology |
| Phase | FDA-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 unwinding and replication. This dual inhibition leads to rapid bactericidal activity against a wide range of gram-positive and gram-negative bacteria, as well as atypical organisms. When applied topically to the eye, it achieves high local concentrations to treat ocular infections.
Approved indications
- Bacterial conjunctivitis (topical ophthalmic)
- Bacterial corneal ulcer (topical ophthalmic)
- Other ocular bacterial infections (topical ophthalmic)
Common side effects
- Conjunctival irritation
- Eye discomfort or pain
- Ocular redness
- Blurred vision
Key clinical trials
- Intrastromal Moxifloxacin as an Adjunctive Therapy in Recalcitrant Bacterial Keratitis (NA)
- Fluorometholone Study (PHASE2)
- Rose Bengal Electromagnetic Activation With Green Light for Infection Reduction (PHASE3)
- Rose Bengal Electromagnetic Activation With Green Light for Infection Reduction II (PHASE3)
- The TRIBECA Study (TRIessence/Byqlovi for Easier CAtaract Surgery) (PHASE4)
- Dropless Pars Plana Vitrectomy Study (PHASE4)
- Study to Evaluate the Safety and Tolerability of PRO-231 Versus VIGAMOXI® on the Ocular Surface of Healthy Subjects (PHASE1)
- Effects of Bromfenac on Macular Thickness After Phacoemulsification Surgery (PHASE4)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Moxifloxacin (Topical) CI brief — competitive landscape report
- Moxifloxacin (Topical) updates RSS · CI watch RSS
- University of California, San Francisco portfolio CI