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Oral Suspension Tedizolid Phosphate

Merck Sharp & Dohme LLC · FDA-approved active Small molecule

Tedizolid phosphate is a prodrug that is converted to tedizolid, an oxazolidinone antibiotic that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit.

Tedizolid phosphate is a prodrug that is converted to tedizolid, an oxazolidinone antibiotic that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. Used for Acute bacterial skin and skin structure infections (ABSSSI), Community-acquired bacterial pneumonia (CABP).

At a glance

Generic nameOral Suspension Tedizolid Phosphate
Also known asSivextro, TR-701 FA, MK-1986
SponsorMerck Sharp & Dohme LLC
Drug classOxazolidinone antibiotic
TargetBacterial 50S ribosomal subunit
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Tedizolid phosphate is rapidly converted to its active form, tedizolid, which binds to the bacterial 50S ribosomal subunit and prevents peptide bond formation, thereby inhibiting protein synthesis. This mechanism is effective against a broad spectrum of gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and other resistant pathogens. The oxazolidinone class represents a unique antibiotic mechanism distinct from other protein synthesis inhibitors.

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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