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Linezolid

FDA-approved product (tablet, oral), marketed as Linezolid, Linezolid In Sodium Chloride 0.9% In Plastic Container, Zyvox.

Registered studies
50+
Lab records
63
Pathogens at ≥40%
2 of 4

Chemical structure

Chemical structure of Linezolid
A drawing shows what the molecule is, not what it does.

Existing / approved use

Documented · FDA, WHO, ChEMBL

Approved for

  • Bacterial disease
  • Bacteriemia
  • Infection
  • Osteomyelitis
  • Pneumonia

Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗

WHO therapeutic group
Other antibacterials
FDA pharmacologic class
Oxazolidinone Antibacterial FDA label ↗
Anti-infective classification
Classified as an existing antimicrobial.WHO ATC J01XX08; FDA class Oxazolidinone Antibacterial

Repurposing investigation

Linezolid is already an antimicrobial, so it is not counted among the repurposing candidates. Its AI-predicted activity is shown below for reference.

AI-predicted activity

AI prediction · nothing measured
  • MRSA89.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
  • E. coli1.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
  • K. pneumoniae27.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
  • M. tuberculosis82.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.

A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.

Evidence

Clinical and experimental

Documented evidence

Clinical

50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.

Experimental

  • MRSA: measured active in 39 of 44 lab records
  • E. coli: measured active in 1 of 4 lab records
  • K. pneumoniae: measured active in 2 of 8 lab records
  • M. tuberculosis: measured active in 5 of 7 lab records
Show the 63 laboratory records, with sources

Loading records…

“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.

Docking

Computational · nothing measured

Dihydrofolate reductase ↗ (E. coli)

-7.0 kcal/mol

0better fit →-12

KPC-2 carbapenemase ↗ (K. pneumoniae)

-7.5 kcal/mol

0better fit →-12

Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)

-7.7 kcal/mol

0better fit →-12

Dihydrofolate reductase ↗ (MRSA)

-7.4 kcal/mol

0better fit →-12

AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.

Other medicines to investigate

AI prediction · nothing measured

Other repurposing candidates: approved medicines besides Linezolid with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.

Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.

Registered studies

A registration describes a study; it does not establish a positive result.

  • An Open-label RCT to Evaluate a New Treatment Regimen for Patients With Multi-drug Resistant Tuberculosis

    NCT02454205 · start 2015-11-12

    Registered record
    Registry ID
    NCT02454205
    Conditions
    Tuberculosis; Multidrug Resistant Tuberculosis; Extensively-drug Resistant Tuberculosis
    Interventions
    Linezolid; Bedaquiline; Levofloxacin; Pyrazinamide; Isoniazid; Ethionamide; Terizidone; Moxifloxacin; Kanamycin
    Study type
    INTERVENTIONAL
    Phase
    Phase 2 / Phase 3
    Registry status
    Completed
    Start
    2015-11-12
    Completion
    2021-08-30
    Enrolment
    154

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionTuberculosis; Multidrug Resistant Tuberculosis; Extensively-drug Resistant Tuberculosis
    InterventionLinezolid; Bedaquiline; Levofloxacin; Pyrazinamide +5 more
    PhasePhase 2 / Phase 3
    Registry statusCompleted
  • Safety and Efficacy of BAY1192631 in Japanese Patients With Methicillin-resistant Staphylococcus Aureus (MRSA) Infections

    NCT01967225 · start 2013-11-23

    Registered record
    Registry ID
    NCT01967225
    Conditions
    Skin Diseases, Infectious
    Interventions
    Tedizolid Phosphate (Sivextro, BAY1192631); Linezolid
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    2013-11-23
    Completion
    2016-10-28
    Enrolment
    125

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionSkin Diseases, Infectious
    InterventionTedizolid Phosphate (Sivextro, BAY1192631); Linezolid
    PhasePhase 3
    Registry statusCompleted
  • Pharmacokinetic and Pharmacodynamic Evaluation of Linezolid Administered Intravenously in MRSA-positive, Morbidly Obese Patients With Pneumonia

    NCT01805284 · start 2013-02

    Registered record
    Registry ID
    NCT01805284
    Conditions
    Pneumonia
    Interventions
    Linezolid
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2013-02
    Completion
    2016-09-30
    Enrolment
    15

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionPneumonia
    InterventionLinezolid
    PhasePhase 4
    Registry statusCompleted
  • Safety and Efficacy of CEM-102 With Rifampin Compared to Standard Therapy in Patients With Prosthetic Joint Infections or Spacer Infection

    NCT01756924 · start 2012-12

    Registered record
    Registry ID
    NCT01756924
    Conditions
    Prosthetic Joint Infections of Hip; Prosthetic Joint Infections of Knee; Infected Spacers
    Interventions
    CEM-102; IV or Oral standard of care antibiotics; Rifampin
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Terminated
    Start
    2012-12
    Completion
    2014-07
    Enrolment
    14

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionProsthetic Joint Infections of Hip; Prosthetic Joint Infections of Knee; Infected Spacers
    InterventionCEM-102; IV or Oral standard of care antibiotics; Rifampin
    PhasePhase 2
    Registry statusTerminated
  • Safety and Efficacy Study of Ceftaroline Versus a Comparator in Pediatric Subjects With Complicated Community Acquired Pneumonia (CABP)

    NCT01669980 · start 2012-10

    Registered record
    Registry ID
    NCT01669980
    Conditions
    Infections; Pneumonia
    Interventions
    Ceftaroline fosamil; IV Ceftriaxone and Vancomycin
    Study type
    INTERVENTIONAL
    Phase
    Phase 4
    Registry status
    Completed
    Start
    2012-10
    Completion
    2014-08
    Enrolment
    40

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionInfections; Pneumonia
    InterventionCeftaroline fosamil; IV Ceftriaxone and Vancomycin
    PhasePhase 4
    Registry statusCompleted
  • Effect of Linezolid on Ex Vivo Neutrophil and Monocyte Function in Healthy Males

    NCT01544673 · start 2012-03

    Registered record
    Registry ID
    NCT01544673
    Conditions
    Gram Positive Infection
    Interventions
    linezolid; Placebo
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    2012-03
    Completion
    2012-04
    Enrolment
    18

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionGram Positive Infection
    Interventionlinezolid; Placebo
    PhasePhase 1
    Registry statusCompleted
  • Asymptomatic Colonization With S. Aureus After Therapy With Linezolid or Clindamycin for Acute Skin Infections

    NCT01619410 · start 2012-01

    Registered record
    Registry ID
    NCT01619410
    Conditions
    Skin Diseases, Bacterial; Abscess
    Interventions
    Linezolid; Clindamycin
    Study type
    INTERVENTIONAL
    Phase
    Not applicable
    Registry status
    Terminated
    Start
    2012-01
    Completion
    2016-12
    Enrolment
    25

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionSkin Diseases, Bacterial; Abscess
    InterventionLinezolid; Clindamycin
    PhaseNot applicable
    Registry statusTerminated
  • TR-701 FA vs Linezolid for the Treatment of Acute Bacterial Skin and Skin Structure Infections

    NCT01421511 · start 2011-09-15

    Registered record
    Registry ID
    NCT01421511
    Conditions
    Skin and Subcutaneous Tissue Bacterial Infections
    Interventions
    TR-701 FA; Linezolid
    Study type
    INTERVENTIONAL
    Phase
    Phase 3
    Registry status
    Completed
    Start
    2011-09-15
    Completion
    2013-01-10
    Enrolment
    666

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionSkin and Subcutaneous Tissue Bacterial Infections
    InterventionTR-701 FA; Linezolid
    PhasePhase 3
    Registry statusCompleted
  • Pharmacokinetics of Linezolid in Children With Cystic Fibrosis

    NCT00625703 · start 2010-12

    Registered record
    Registry ID
    NCT00625703
    Conditions
    Cystic Fibrosis
    Interventions
    Linezolid
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    2010-12
    Completion
    2011-05
    Enrolment
    45

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionCystic Fibrosis
    InterventionLinezolid
    PhasePhase 2
    Registry statusCompleted
  • Clinical Trials to Reduce the Risk of Antimicrobial Resistance

    NCT01570192 · start 2010-09

    Registered record
    Registry ID
    NCT01570192
    Conditions
    Bacterial Pneumonia
    Interventions
    IV meropenem; I.V. Meropenem; Parenteral aminoglycoside; tobramycin for injection USP OR gentamicin sulfate injection solution concentrate 5mg.kg IV q24h; amikacin sulfate injection USP 20 mg/kg IV q24h; Linezolid or Vancomycin (per institutional guidelines) will be available for MRSA coverage.; tobramycin nebulization
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Terminated
    Start
    2010-09
    Completion
    2015-04
    Enrolment
    43

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionBacterial Pneumonia
    InterventionIV meropenem; I.V. Meropenem; Parenteral aminoglycoside; tobramycin for injection USP OR gentamicin sulfate injection solution concentrate 5mg.kg IV q24h +3 more
    PhasePhase 2
    Registry statusTerminated
  • Efficacy and Safety Study of JNJ-32729463 for Treating Complicated Skin and Skin Structure Infections Compared to Linezolid (Zyvox)

    NCT01128530 · start 2010-06

    Registered record
    Registry ID
    NCT01128530
    Conditions
    Complicated Skin and Skin Structure Infections
    Interventions
    JNJ-32729463; linezolid; JNJ-32729463 placebo; linezolid placebo
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    2010-06
    Completion
    2011-01
    Enrolment
    161

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionComplicated Skin and Skin Structure Infections
    InterventionJNJ-32729463; linezolid; JNJ-32729463 placebo; linezolid placebo
    PhasePhase 2
    Registry statusCompleted
  • Bioequivalence Study Comparing Linezolid 600 Mg Oral Suspension With 600 Mg Tablet In Chinese Healthy Male Subjects

    NCT01055769 · start 2010-03

    Registered record
    Registry ID
    NCT01055769
    Conditions
    Healthy Volunteers
    Interventions
    Linezolid; Linezolid
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Completed
    Start
    2010-03
    Completion
    2010-04
    Enrolment
    20

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionHealthy Volunteers
    InterventionLinezolid; Linezolid
    PhasePhase 1
    Registry statusCompleted
  • A Single Center Four Part Study in Healthy Adult Subjects to Evaluate: the Safety, Tolerability and Pharmacokinetics of a Single Oral Dose and Repeat Escalating Oral Doses of GSK945237; the Effect of Linezolid on Hematology Safety Parameters; and the Effects of GSK945237 and Moxifloxacin on QTc.

    NCT01039610 · start 2009-11

    Registered record
    Registry ID
    NCT01039610
    Conditions
    Infections, Bacterial
    Interventions
    GSK945237; Placebo; Linezolid; Moxifloxacin
    Study type
    INTERVENTIONAL
    Phase
    Phase 1
    Registry status
    Withdrawn
    Start
    2009-11
    Completion
    2010-08
    Enrolment
    0

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionInfections, Bacterial
    InterventionGSK945237; Placebo; Linezolid; Moxifloxacin
    PhasePhase 1
    Registry statusWithdrawn
  • TBTC Study 30: Safety and Tolerability of Low Dose Linezolid in MDR TB

    NCT00664313 · start 2009-04

    Registered record
    Registry ID
    NCT00664313
    Conditions
    Multi-drug Resistant Tuberculosis; Extensively Drug Resistant Tuberculosis
    Interventions
    Linezolid; Placebo
    Study type
    INTERVENTIONAL
    Phase
    Phase 1 / Phase 2
    Registry status
    Completed
    Start
    2009-04
    Completion
    2010-09
    Enrolment
    36

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionMulti-drug Resistant Tuberculosis; Extensively Drug Resistant Tuberculosis
    InterventionLinezolid; Placebo
    PhasePhase 1 / Phase 2
    Registry statusCompleted
  • Study the Efficacy and Safety of PTK 0796 in Patients With Complicated Skin and Skin Structure Infection (CSSSI)

    NCT03716024 · start 2007-07-18

    Registered record
    Registry ID
    NCT03716024
    Conditions
    Infectious Skin Disease; Bacterial Skin Disease
    Interventions
    PTK 0796; Linezolid
    Study type
    INTERVENTIONAL
    Phase
    Phase 2
    Registry status
    Completed
    Start
    2007-07-18
    Completion
    2008-01-07
    Enrolment
    234

    As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.

    ConditionInfectious Skin Disease; Bacterial Skin Disease
    InterventionPTK 0796; Linezolid
    PhasePhase 2
    Registry statusCompleted