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Cefazolin and Moxifloxacin — Competitive Intelligence Brief
phase 3
Beta-lactam antibiotic + Fluoroquinolone combination
Bacterial penicillin-binding proteins (cefazolin); bacterial DNA gyrase and topoisomerase IV (moxifloxacin)
Infectious Disease
Small molecule
Live · refreshed every 30 min
Target snapshot
Cefazolin and Moxifloxacin (Cefazolin and Moxifloxacin) — University of British Columbia. This combination uses cefazolin (a beta-lactam antibiotic) to inhibit bacterial cell wall synthesis and moxifloxacin (a fluoroquinolone) to inhibit bacterial DNA gyrase and topoisomerase IV, providing broad-spectrum antimicrobial coverage.
Comparator set
| Drug | Generic | Sponsor | Phase | Class | Target | Approval / PDUFA |
|---|---|---|---|---|---|---|
| Cefazolin and Moxifloxacin TARGET | Cefazolin and Moxifloxacin | University of British Columbia | phase 3 | Beta-lactam antibiotic + Fluoroquinolone combination | Bacterial penicillin-binding proteins (cefazolin); bacterial DNA gyrase and topoisomerase IV (moxifloxacin) |
Recent regulatory actions (last 90 days)
Upcoming PDUFA dates (next 180 days)
Patent timeline (forward window)
Sponsor landscape (Beta-lactam antibiotic + Fluoroquinolone combination class)
- University of British Columbia · 1 drug in this class
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Cite this brief
Drug Landscape (2026). Cefazolin and Moxifloxacin — Competitive Intelligence Brief. https://druglandscape.com/ci/cefazolin-and-moxifloxacin. Accessed 2026-05-16.
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