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Fosfomycin sodium intravenous

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla · Phase 3 active Small molecule

Fosfomycin inhibits bacterial cell wall synthesis by inactivating the MurA enzyme, preventing peptidoglycan cross-linking.

Fosfomycin inhibits bacterial cell wall synthesis by inactivating the MurA enzyme, preventing peptidoglycan cross-linking. Used for Serious bacterial infections caused by susceptible pathogens, Multidrug-resistant gram-negative infections.

At a glance

Generic nameFosfomycin sodium intravenous
Also known asGeneric name: Fosfomycin, Pharmaceutical form: solution for infusion, ATC code: J01J3
SponsorFundación Pública Andaluza para la gestión de la Investigación en Sevilla
Drug classCell wall synthesis inhibitor
TargetMurA (UDP-N-acetylglucosamine enolpyruvyl transferase)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

Fosfomycin is a broad-spectrum antibiotic that acts as a phosphoenolpyruvate (PEP) analogue, irreversibly inhibiting UDP-N-acetylglucosamine enolpyruvyl transferase (MurA), a key enzyme in bacterial peptidoglycan biosynthesis. This disruption of cell wall formation leads to bacterial cell lysis and death. The intravenous sodium formulation allows systemic delivery for treatment of 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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