Imipenem
FDA-approved product (powder, intravenous).
- Registered studies
- 50+
- Lab records
- 505
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Endocarditis
- Infection
- Pneumonia
- Sepsis
- Urinary tract 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 J01DH51
Repurposing investigation
Imipenem 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- MRSA62.6% 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. coli97.4% 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.
- K. pneumoniae96.2% 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. tuberculosis31.0% AI-predicted activityBelow 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
- MRSA: measured active in 44 of 77 lab records
- E. coli: measured active in 86 of 94 lab records
- K. pneumoniae: measured active in 247 of 334 lab records
Show the latest 150 of 505 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 Imipenem 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.
- ApalutamideExisting use: Cancer, Metastatic prostate cancer, Neoplasm and 3 more67.6% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Clomipramine HydrochlorideExisting use: Depressive disorder, Major depressive disorder, Obsessive-compulsive disorder67.6% AI-predicted activityagainst M. tuberculosis33 registered studies
- Pazopanib HydrochlorideExisting use: Chromophobe renal cell carcinoma, Clear cell renal carcinoma, Collecting duct carcinoma and 4 more67.6% AI-predicted activityagainst M. tuberculosis50+ registered studies
- CyclothiazideExisting use: Cardiovascular disease67.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- Vincristine SulfateExisting use: Neoplasm67.6% AI-predicted activityagainst M. tuberculosis50+ registered studies
- VenetoclaxExisting use: Cancer, Chronic lymphocytic leukemia, Neoplasm67.5% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AmprenavirExisting use: HIV infection, Viral disease67.4% AI-predicted activityagainst M. tuberculosis50+ registered studies
- IndapamideExisting use: Cardiovascular disease, Congestive heart failure, Hypertension and 1 more67.3% AI-predicted activityagainst M. tuberculosis50+ registered studies
- AfamelanotideExisting use: Erythropoietic protoporphyria66.9% AI-predicted activityagainst M. tuberculosis23 registered studies
- PerphenazineExisting use: Nausea and vomiting, Psychosis, Schizophrenia66.9% AI-predicted activityagainst M. tuberculosis34 registered studies
- Dabigatran Etexilate MesylateExisting use: Atrial fibrillation, Deep vein thrombosis, Pulmonary embolism and 5 more66.9% AI-predicted activityagainst M. tuberculosis14 registered studies
- Infigratinib PhosphateExisting use: Cancer, Cholangiocarcinoma, Intrahepatic cholangiocarcinoma and 1 more66.8% AI-predicted activityagainst M. tuberculosis2 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Efficacy and Safety of Imipenem+Cilastatin/Relebactam (MK-7655A) Versus Colistimethate Sodium+Imipenem+Cilastatin in Imipenem-Resistant Bacterial Infection (MK-7655A-013)
NCT02452047 · start 2015-08-21
Registered record
- Registry ID
- NCT02452047
- Conditions
- Bacterial Infections
- Interventions
- Imipenem+Cilastatin/Relebactam; Colistimethate sodium (CMS); Imipenem+Cilastatin; Placebo to CMS
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2015-08-21
- Completion
- 2017-09-18
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBacterial InfectionsInterventionImipenem+Cilastatin/Relebactam; Colistimethate sodium (CMS); Imipenem+Cilastatin; Placebo to CMSPhasePhase 3Registry statusCompletedA Study of Efficacy and Safety of Intravenous Cefiderocol (S-649266) Versus Imipenem/Cilastatin in Complicated Urinary Tract Infections
NCT02321800 · start 2015-02-05
Registered record
- Registry ID
- NCT02321800
- Conditions
- Urinary Tract Infections
- Interventions
- Cefiderocol; Imipenem/cilastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2015-02-05
- Completion
- 2016-08-16
- Enrolment
- 452
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUrinary Tract InfectionsInterventionCefiderocol; Imipenem/cilastatinPhasePhase 2Registry statusCompletedPreliminary Research On Two-step Dosing Of Imipenem/Cilastatin
NCT02616354 · start 2015-01
Registered record
- Registry ID
- NCT02616354
- Conditions
- Sepsis
- Interventions
- Imipenem
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2015-01
- Completion
- 2015-12
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSepsisInterventionImipenemPhasePhase 4Registry statusUnknownImipenem Prophylaxis in Patients With Acute Pancreatitis
NCT02897206 · start 2014-10
Registered record
- Registry ID
- NCT02897206
- Conditions
- Acute Pancreatitis
- Interventions
- Imipenem; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-10
- Completion
- 2016-12
- Enrolment
- 98
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute PancreatitisInterventionImipenem; PlaceboPhasePhase 4Registry statusCompletedEffect Study of Tigecycline to Treat Severe Sepsis and Septic Shock
NCT02191475 · start 2014-05
Registered record
- Registry ID
- NCT02191475
- Conditions
- Abdominal Infection
- Interventions
- glycopeptide plus carbapenem; Haizheng Li Xing ® plus tazocin ®
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2014-05
- Completion
- 2017-05
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAbdominal InfectionInterventionglycopeptide plus carbapenem; Haizheng Li Xing ® plus tazocin ®PhasePhase 2 / Phase 3Registry statusUnknownPharmacokinetics of Imipenem During Ex Vivo Lung Perfusion (EVLP)
NCT02670239 · start 2014-05
Registered record
- Registry ID
- NCT02670239
- Conditions
- Lung Transplantation
- Interventions
- normothermic ex vivo lung perfusion
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2014-05
- Completion
- Not recorded
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLung TransplantationInterventionnormothermic ex vivo lung perfusionPhaseNot recordedRegistry statusUnknownPatients Response to Early Switch To Oral:Osteomyelitis Study
NCT02099240 · start 2014-03-06
Registered record
- Registry ID
- NCT02099240
- Conditions
- Osteomyelitis
- Interventions
- oral antibiotics; intravenous antibiotics
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Terminated
- Start
- 2014-03-06
- Completion
- 2018-11-07
- Enrolment
- 11
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteomyelitisInterventionoral antibiotics; intravenous antibioticsPhaseEarly phase 1Registry statusTerminatedEffect of Aerosolised Colistin in Ventilator Associated Pneumonia
NCT02683603 · start 2013-04
Registered record
- Registry ID
- NCT02683603
- Conditions
- Pneumonia, Ventilator-Associated
- Interventions
- AS colistin and "imipenem"; IV colistin " and "imipenem" .; AS colimycin (colistin); IV colimycin (colistin); AS colistin and imipenem; IV colistin and imipenem
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2013-04
- Completion
- 2015-04
- Enrolment
- 133
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPneumonia, Ventilator-AssociatedInterventionAS colistin and "imipenem"; IV colistin " and "imipenem" .; AS colimycin (colistin); IV colimycin (colistin) +2 morePhasePhase 4Registry statusCompletedA Comparative Study of ID Fellow-based VS. Pharmacist-based Antibiotic Pre-authorization
NCT01797133 · start 2013-02
Registered record
- Registry ID
- NCT01797133
- Conditions
- All Hospitalzied Patients; No Specific Conditions Requires
- Interventions
- ID fellow-based antibiotic pre-authorization; Pharmacist-based antibiotic pre-authorization
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2013-02
- Completion
- 2013-12
- Enrolment
- 984
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAll Hospitalzied Patients; No Specific Conditions RequiresInterventionID fellow-based antibiotic pre-authorization; Pharmacist-based antibiotic pre-authorizationPhaseNot applicableRegistry statusCompletedPiperacillin/Tazobactam for Empirical Therapy of Febrile Neutropenia
NCT01714570 · start 2012-11
Registered record
- Registry ID
- NCT01714570
- Conditions
- Febrile; Neutropenia; Hematopoietic Stem Cell Transplantation
- Interventions
- Piperacillin-tazobactam combination product; Imipenem
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2012-11
- Completion
- 2014-04
- Enrolment
- 123
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFebrile; Neutropenia; Hematopoietic Stem Cell TransplantationInterventionPiperacillin-tazobactam combination product; ImipenemPhaseNot applicableRegistry statusCompletedEmergence of Resistance in Intestinal Microflora During Carbapenem Treatments
NCT01703299 · start 2012-10
Registered record
- Registry ID
- NCT01703299
- Conditions
- Carbapenem-induced Resistance
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2012-10
- Completion
- 2014-03
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCarbapenem-induced ResistanceInterventionNot recordedPhaseNot recordedRegistry statusCompletedAntibiotic Prophylaxis for Transrectal Prostate Biopsy
NCT01659866 · start 2012-08
Registered record
- Registry ID
- NCT01659866
- Conditions
- Infection
- Interventions
- Ciprofloxacin; trimethoprim-sulfamethoxazole; cefuroxime; ceftriaxone; gentamicin; amikacin; aztreonam; imipenem; ceftriaxone; gentamicin; amikacin; aztreonam; imipenem
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2012-08
- Completion
- 2016-08
- Enrolment
- 563
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfectionInterventionCiprofloxacin; trimethoprim-sulfamethoxazole; cefuroxime; ceftriaxone +9 morePhasePhase 4Registry statusCompletedSafety, Tolerability, and Efficacy of MK-7655 (Relebactam) + Imipenem/Cilastatin Versus Imipenem/Cilastatin Alone for Treating Complicated Urinary Tract Infection (cUTI) (MK-7655-003)
NCT01505634 · start 2012-05-16
Registered record
- Registry ID
- NCT01505634
- Conditions
- Urinary Tract Infections; Pyelonephritis
- Interventions
- Relebactam 250 mg; Relebactam 125 mg; imipenem/cilastatin 500 mg; Placebo to relebactam; Ciprofloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2012-05-16
- Completion
- 2015-07-28
- Enrolment
- 302
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUrinary Tract Infections; PyelonephritisInterventionRelebactam 250 mg; Relebactam 125 mg; imipenem/cilastatin 500 mg; Placebo to relebactam +1 morePhasePhase 2Registry statusCompletedA Single-Dose Study to Investigate the Pharmacokinetics of MK-7655 in Participants With Impaired Renal Function (MK-7655-005)
NCT01275170 · start 2011-01-28
Registered record
- Registry ID
- NCT01275170
- Conditions
- Infectious Disease
- Interventions
- MK-7655; Imipenem + Cilastatin; Caffeine; Midazolam; Omeprazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-01-28
- Completion
- 2012-03-05
- Enrolment
- 49
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfectious DiseaseInterventionMK-7655; Imipenem + Cilastatin; Caffeine; Midazolam +1 morePhasePhase 1Registry statusCompletedComparative Study of NXL104/Ceftazidime Versus Comparator in Adults With Complicated Urinary Tract Infections
NCT00690378 · start 2008-11
Registered record
- Registry ID
- NCT00690378
- Conditions
- Complicated Urinary Tract Infection
- Interventions
- NXL104/ceftazidime; Imipenem/Cilastatin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2008-11
- Completion
- 2010-07
- Enrolment
- 137
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Urinary Tract InfectionInterventionNXL104/ceftazidime; Imipenem/CilastatinPhasePhase 2Registry statusCompleted