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Cefazolin and Moxifloxacin

University of British Columbia · Phase 3 active Small molecule

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.

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. Used for Surgical site infection prophylaxis (likely indication given Phase 3 status and combination rationale), Serious gram-positive and gram-negative bacterial infections.

At a glance

Generic nameCefazolin and Moxifloxacin
SponsorUniversity of British Columbia
Drug classBeta-lactam antibiotic + Fluoroquinolone combination
TargetBacterial penicillin-binding proteins (cefazolin); bacterial DNA gyrase and topoisomerase IV (moxifloxacin)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Cefazolin is a first-generation cephalosporin that binds penicillin-binding proteins and prevents peptidoglycan cross-linking in bacterial cell walls, leading to cell lysis. Moxifloxacin is a fourth-generation fluoroquinolone that inhibits bacterial topoisomerases, preventing DNA replication and transcription. Together, they provide synergistic coverage against gram-positive and gram-negative bacteria, likely being evaluated for surgical prophylaxis or serious 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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