Last reviewed · How we verify

Tedizolid IV

University of Southern California · FDA-approved active Small molecule

Tedizolid inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit, preventing peptide bond formation.

Tedizolid inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit, preventing peptide bond formation. Used for Acute bacterial skin and skin structure infections (ABSSSI), Community-acquired bacterial pneumonia (CABP).

At a glance

Generic nameTedizolid IV
Also known asSivextro, TR-701 FA, MK-1986
SponsorUniversity of Southern California
Drug classOxazolidinone antibiotic
TargetBacterial 50S ribosomal subunit
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Tedizolid is an oxazolidinone antibiotic that binds to the bacterial 50S ribosomal subunit and inhibits the initiation of protein synthesis. This mechanism is bacteriostatic, halting bacterial growth and allowing the immune system to clear the infection. Tedizolid is a prodrug that is converted to its active form in vivo and has enhanced potency and pharmacokinetics compared to linezolid, its predecessor.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: