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Levofloxacin + Ceftriaxone

Bayer · Phase 3 active Small molecule

This combination uses a fluoroquinolone antibiotic to inhibit bacterial DNA gyrase and topoisomerase IV, while a third-generation cephalosporin inhibits bacterial cell wall synthesis, providing broad-spectrum coverage against gram-positive and gram-negative bacteria.

This combination uses a fluoroquinolone antibiotic to inhibit bacterial DNA gyrase and topoisomerase IV, while a third-generation cephalosporin inhibits bacterial cell wall synthesis, providing broad-spectrum coverage against gram-positive and gram-negative bacteria. Used for Community-acquired pneumonia, Complicated urinary tract infections, Intra-abdominal infections.

At a glance

Generic nameLevofloxacin + Ceftriaxone
SponsorBayer
Drug classFluoroquinolone + Third-generation cephalosporin combination
TargetBacterial DNA gyrase, topoisomerase IV, penicillin-binding proteins
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Levofloxacin is a fluoroquinolone that disrupts bacterial DNA replication by inhibiting topoisomerases, while ceftriaxone is a beta-lactam antibiotic that binds penicillin-binding proteins and prevents peptidoglycan cross-linking in the bacterial cell wall. Together, they provide synergistic bactericidal activity against a wide range of aerobic and some anaerobic pathogens, reducing the likelihood of resistance development.

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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