Ertapenem Sodium
FDA-approved product (injectable, intramuscular, intravenous), marketed as Ertapenem Sodium, Invanz.
- Registered studies
- 50+
- Lab records
- 186
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Bacterial disease
- Bacterial pneumonia
- Community-Acquired Infections
- Gram-negative bacterial infections
- Infection
- Osteomyelitis
- Staphylococcal skin infections
- Streptococcal infection
- Surgical Wound Infection
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Carbapenems
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J01DH03
Repurposing investigation
Ertapenem Sodium 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- MRSA98.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli98.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. A stereoisomer of this medicine was in the model's training data.
- K. pneumoniae99.0% 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.
- M. tuberculosis55.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
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
- K. pneumoniae: measured active in 141 of 186 lab records
Show the latest 150 of 186 laboratory records, with sources
Loading records…
Every record is in ChEMBL, linked above. “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 measuredAutoDock 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 measuredOther repurposing candidates: approved medicines besides Ertapenem Sodium 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.
- DichlorphenamideExisting use: Glaucoma73.9% AI-predicted activityagainst M. tuberculosisLab records exist2 registered studies
- Tamsulosin HydrochlorideExisting use: Benign prostatic hyperplasia, Prostate carcinoma73.2% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Thiethylperazine MalateExisting use: Allergic disease71.8% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SaquinavirExisting use: HIV infection, HIV-1 infection, Viral disease71.5% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AvacopanExisting use: Anti-neutrophil antibody associated vasculitis, Anti-neutrophil cytoplasmic antibody-associated vasculitis, Granulomatosis with Polyangiitis and 1 more71.3% AI-predicted activityagainst M. tuberculosis26 registered studies
- Lasmiditan SuccinateExisting use: Migraine disorder71.0% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma71.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Vinblastine SulfateExisting use: Classic Hodgkin lymphoma, Fungal infectious disease, Hodgkins lymphoma and 3 more70.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Haloperidol DecanoateExisting use: Conduct disorder, Mental or behavioural disorder, Psychosis and 4 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- HydrochlorothiazideExisting use: Angina pectoris, Cardiovascular disease, Chronic kidney disease and 9 more70.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
- TolvaptanExisting use: Autosomal dominant polycystic kidney disease, Cardiovascular disease, Congestive heart failure and 4 more70.0% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Larotrectinib SulfateExisting use: Abdominal Neoplasms, Cancer, Metastasis and 1 more69.2% AI-predicted activityagainst M. tuberculosis5 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Study to Evaluate the Duration of Treatment With Ertapenem in Acute Attacks of Sigmoid Diverticulitis
NCT00097734 · start 2004-07
Registered record
- Registry ID
- NCT00097734
- Conditions
- Diverticulitis, Colonic; Acute Disease
- Interventions
- ertapenem
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2004-07
- Completion
- 2007-06
- Enrolment
- 540
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiverticulitis, Colonic; Acute DiseaseInterventionertapenemPhasePhase 4Registry statusUnknownAn Investigational Agent for the Treatment of Complicated Intra-Abdominal Infections or Acute Pelvic Infections (0826-038)
NCT00092170 · start 2002-03
Registered record
- Registry ID
- NCT00092170
- Conditions
- Infections; Pelvic Infections
- Interventions
- MK0826, ertapenem sodium; Comparator: Ticarcillin/Clavulanate
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2002-03
- Completion
- 2004-01
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfections; Pelvic InfectionsInterventionMK0826, ertapenem sodium; Comparator: Ticarcillin/ClavulanatePhasePhase 2Registry statusCompletedErtapenem Study in Pediatric Patients Who Have Urinary Tract Infections, Skin Infections or Community-acquired Pneumonia (0826-036)
NCT00451386 · start 2002-01
Registered record
- Registry ID
- NCT00451386
- Conditions
- Urinary Tract Infections; Bacterial Pneumonia; Soft Tissue Infections
- Interventions
- MK0826, ertapenem sodium /Duration of Treatment: 14 Days; Comparator: ceftriaxone sodium /Duration of Treatment: 14 Days
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2002-01
- Completion
- 2003-12
- Enrolment
- 400
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUrinary Tract Infections; Bacterial Pneumonia; Soft Tissue InfectionsInterventionMK0826, ertapenem sodium /Duration of Treatment: 14 Days; Comparator: ceftriaxone sodium /Duration of Treatment: 14 DaysPhasePhase 2Registry statusCompletedErtapenem Sodium vs. Piperacillin/Tazobactam in the Treatment of Complicated Intra-Abdominal Infections (0826-037)
NCT00389987 · start 2001-09
Registered record
- Registry ID
- NCT00389987
- Conditions
- Complicated Intra-Abdominal Infections
- Interventions
- MK0826, /Duration of Treatment : 8 Weeks; Comparator : piperacillin sodium (+) tazobactam sodium /Duration of Treatment : 8 Weeks
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2001-09
- Completion
- 2004-05
- Enrolment
- 300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Intra-Abdominal InfectionsInterventionMK0826, /Duration of Treatment : 8 Weeks; Comparator : piperacillin sodium (+) tazobactam sodium /Duration of Treatment : 8 WeeksPhasePhase 3Registry statusCompletedComparison of Ertapenem Distribution in the Muscle of Six Healthy Volunteers and Six Critically Ill Patients by Microdialysis
NCT01061047
Registered record
- Registry ID
- NCT01061047
- Conditions
- Healthy
- Interventions
- Ertapeneme
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- Not recorded
- Completion
- Not recorded
- Enrolment
- Not recorded
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionErtapenemePhasePhase 1Registry statusCompleted