Ceftazidime
FDA-approved product (injectable, injection), marketed as Ceftazidime, Ceftazidime In Dextrose Container, Ceptaz and 7 more.
- Registered studies
- 50+
- Lab records
- 324
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Bacterial disease
- Infection
- Parametritis
- Peritonitis
- Pneumonia
- Pyelonephritis
- Urinary tract infection
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Third-generation cephalosporins
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J01DD02
Repurposing investigation
Ceftazidime 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- MRSA94.2% 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.
- E. coli>99% 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. pneumoniae60.1% 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. tuberculosis53.5% 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
- MRSA: measured active in 5 of 5 lab records
- E. coli: measured active in 41 of 47 lab records
- K. pneumoniae: measured active in 111 of 272 lab records
Show the latest 150 of 324 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 measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
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 measuredOther repurposing candidates: approved medicines besides Ceftazidime 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.
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm95.6% AI-predicted activityagainst MRSALab records exist50+ registered studies
- TaurursodiolExisting use: Bile acids and derivatives79.6% AI-predicted activityagainst MRSA43 registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome74.5% AI-predicted activityagainst MRSA50+ registered studies
- PlecanatideExisting use: Constipation74.4% AI-predicted activityagainst MRSA15 registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia74.2% AI-predicted activityagainst MRSA50+ registered studies
- PosaconazoleExisting use: Aspergillosis, Candidiasis, Coccidioidomycosis and 2 more72.2% AI-predicted activityagainst MRSA50+ registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma70.6% AI-predicted activityagainst MRSA50+ registered studies
- TemsirolimusExisting use: Cancer, Clear cell renal carcinoma, Mantle cell lymphoma and 2 more70.1% AI-predicted activityagainst MRSA50+ registered studies
- Quizartinib DihydrochlorideExisting use: Acute myeloid leukemia, Myeloid leukemia70.0% AI-predicted activityagainst MRSA4 registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more70.0% AI-predicted activityagainst MRSA50+ registered studies
- Deoxycholic AcidExisting use: Other dermatologicals69.3% AI-predicted activityagainst MRSA50+ registered studies
- ChenodiolExisting use: Cerebrotendinous xanthomatosis, Inborn errors of metabolism69.2% AI-predicted activityagainst MRSA30 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Evaluation of Safety,Pharmacokinetics and Efficacy of CAZ-AVI With Metronidazole in Children Aged 3 Months to 18 Years Old With Complicated Intra-abdominal Infections (cIAIs).
NCT02475733 · start 2015-08-01
Registered record
- Registry ID
- NCT02475733
- Conditions
- Complicated Intra-abdominal Infections
- Interventions
- Ceftazidime -avibactam; Meropenem; Metronidazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2015-08-01
- Completion
- 2017-06-01
- Enrolment
- 83
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Intra-abdominal InfectionsInterventionCeftazidime -avibactam; Meropenem; MetronidazolePhasePhase 2Registry statusCompletedComparing Cefepime Versus Cefazolin Plus Ceftazidime for CAPD-associated Peritonitis
NCT02872038 · start 2015-08
Registered record
- Registry ID
- NCT02872038
- Conditions
- Peritoneal Dialysis Associated Peritonitis
- Interventions
- Cefepime; Cefazolin plus Ceftazidime
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2015-08
- Completion
- 2016-11-30
- Enrolment
- 154
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPeritoneal Dialysis Associated PeritonitisInterventionCefepime; Cefazolin plus CeftazidimePhasePhase 4Registry statusCompletedA Phase I Study to Assess the Safety, Tolerability and PK of Ceftazidime-Avibactam in Healthy Chinese Subjects
NCT01920399 · start 2013-10
Registered record
- Registry ID
- NCT01920399
- Conditions
- Healthy Volunteers
- Interventions
- CAZ-AVI; 0.9% Normal Saline
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-10
- Completion
- 2013-11
- Enrolment
- 42
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteersInterventionCAZ-AVI; 0.9% Normal SalinePhasePhase 1Registry statusCompletedA Study to Investigate the Effect of Administration of Ceftazidime-avibactam (CAZ-AVI) and Ceftaroline Fosamil -Avibactam (CXL) on the Intestinal Flora of Healthy Volunteers
NCT01789528 · start 2013-08
Registered record
- Registry ID
- NCT01789528
- Conditions
- Pharmacokinetics; Open Label; CAZ-AVI; CXL; Effect on Intestinal Flora; Safety
- Interventions
- CAZ-AVI; CXL
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-08
- Completion
- 2014-03
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPharmacokinetics; Open Label; CAZ-AVI; CXL +2 moreInterventionCAZ-AVI; CXLPhasePhase 1Registry statusCompletedPharmacokinetics of Selected Antiinfectives During Sustained Low-efficiency Dialysis (SLED)
NCT02287493 · start 2013-07
Registered record
- Registry ID
- NCT02287493
- Conditions
- Replacement Therapy, Renal
- Interventions
- Pharmacokinetic Analysis
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2013-07
- Completion
- 2016-12
- Enrolment
- 35
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionReplacement Therapy, RenalInterventionPharmacokinetic AnalysisPhaseNot recordedRegistry statusCompletedCeftazidime-Avibactam for the Treatment of Infections Due to Ceftazidime Resistant Pathogens
NCT01644643 · start 2013-01
Registered record
- Registry ID
- NCT01644643
- Conditions
- Complicated Urinary Tract Infection; Complicated Intra-abdominal Infection
- Interventions
- Ceftazidime - Avibactam ( CAZ-AVI); Best Available Therapy; Metronidazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2013-01
- Completion
- 2014-09
- Enrolment
- 345
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Urinary Tract Infection; Complicated Intra-abdominal InfectionInterventionCeftazidime - Avibactam ( CAZ-AVI); Best Available Therapy; MetronidazolePhasePhase 3Registry statusCompletedCeftazidime-Avibactam Compared With Doripenem Followed by Oral Therapy for Hospitalized Adults With Complicated UTIs (Urinary Tract Infections)
NCT01595438 · start 2012-10
Registered record
- Registry ID
- NCT01595438
- Conditions
- Complicated Urinary Tract Infection (cUTI) Including Acute Pyelonephritis
- Interventions
- Ceftazidime - Avibactam ( CAZ-AVI); Doripenem; Either switch to oral therapy: 500 mg of Ciprofloxacin (oral); or switch to oral therapy: 800 mg/160 mg of sulfamethoxazole/trimethoprim (oral)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2012-10
- Completion
- 2014-08
- Enrolment
- 598
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Urinary Tract Infection (cUTI) Including Acute PyelonephritisInterventionCeftazidime - Avibactam ( CAZ-AVI); Doripenem; Either switch to oral therapy: 500 mg of Ciprofloxacin (oral); or switch to oral therapy: 800 mg/160 mg of sulfamethoxazole/trimethoprim (oral)PhasePhase 3Registry statusCompletedCeftazidime-Avibactam Compared With Doripenem Followed by Oral Therapy for Hospitalized Adults With Complicated UTIs (Urinary Tract Infections)
NCT01599806 · start 2012-10
Registered record
- Registry ID
- NCT01599806
- Conditions
- Complicated Urinary Tract Infection (cUTI) Including Acute Pyelonephritis
- Interventions
- Ceftazidime - Avibactam ( CAZ-AVI); Doripenem; Either switch to oral therapy: 500 mg of Ciprofloxacin (oral); or switch to oral therapy: 800 mg/160 mg of sulfamethoxazole/trimethoprim (oral)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2012-10
- Completion
- 2014-08
- Enrolment
- 641
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Urinary Tract Infection (cUTI) Including Acute PyelonephritisInterventionCeftazidime - Avibactam ( CAZ-AVI); Doripenem; Either switch to oral therapy: 500 mg of Ciprofloxacin (oral); or switch to oral therapy: 800 mg/160 mg of sulfamethoxazole/trimethoprim (oral)PhasePhase 3Registry statusCompletedCompare Ceftazidime-Avibactam + Metronidazole Versus Meropenem for Hospitalized Adults With Complicated Intra-Abdominal Infections
NCT01499290 · start 2012-03
Registered record
- Registry ID
- NCT01499290
- Conditions
- Complicated Intra-Abdominal Infection
- Interventions
- CAZ-AVI; Metronidazole; Meropenem
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2012-03
- Completion
- 2014-04
- Enrolment
- 493
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Intra-Abdominal InfectionInterventionCAZ-AVI; Metronidazole; MeropenemPhasePhase 3Registry statusCompletedA Study to Assess the Levels of CAZ-AVI and Metronidazole in the Blood When Given Together and Separately
NCT01534247 · start 2012-02
Registered record
- Registry ID
- NCT01534247
- Conditions
- Healthy
- Interventions
- CAZ-AVI; metronidazole; CAZ-AVI + metronidazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2012-02
- Completion
- 2012-07
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionCAZ-AVI; metronidazole; CAZ-AVI + metronidazolePhasePhase 1Registry statusCompletedPharmacokinetic Assessment of Ceftazidime in Intermittent Hemodialysis Patients
NCT01507532 · start 2012-01
Registered record
- Registry ID
- NCT01507532
- Conditions
- Renal Failure
- Interventions
- pharmacokinetic monitoring
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2012-01
- Completion
- 2016-01
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRenal FailureInterventionpharmacokinetic monitoringPhasePhase 4Registry statusWithdrawnA Study to Assess the Levels of Two Antibiotics in the Blood When Given Together and Separately
NCT01430910 · start 2011-09
Registered record
- Registry ID
- NCT01430910
- Conditions
- Healthy
- Interventions
- CAZ104; Avibactam; Ceftazidime
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-09
- Completion
- 2012-10
- Enrolment
- 43
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionCAZ104; Avibactam; CeftazidimePhasePhase 1Registry statusCompletedPopulation Pharmacokinetics of Anti-infectious Drugs in Children
NCT01344512 · start 2011-06
Registered record
- Registry ID
- NCT01344512
- Conditions
- Pediatrics; Ceftazidime; Ciprofloxacin; Voriconazole
- Interventions
- Ceftazidime; Ciprofloxacin; Voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2011-06
- Completion
- 2014-09
- Enrolment
- 214
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediatrics; Ceftazidime; Ciprofloxacin; VoriconazoleInterventionCeftazidime; Ciprofloxacin; VoriconazolePhaseNot applicableRegistry statusCompletedSafety and Efficacy of IV CXA-101 and IV Ceftazidime in Patients With Complicated Urinary Tract Infections
NCT00921024 · start 2009-06-30
Registered record
- Registry ID
- NCT00921024
- Conditions
- Complicated Urinary Tract Infection
- Interventions
- CXA-101; Ceftazidime
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2009-06-30
- Completion
- 2010-03-11
- Enrolment
- 129
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Urinary Tract InfectionInterventionCXA-101; CeftazidimePhasePhase 2Registry statusCompletedProspective Randomized Evaluation of Antibiotic Regimen Following Appendectomy for Perforated Appendicitis
NCT00195923 · start 2005-04
Registered record
- Registry ID
- NCT00195923
- Conditions
- Perforated Appendicitis
- Interventions
- Ampicillin, gentamicin, clindamycin, flagyl, ceftazidime
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2005-04
- Completion
- 2007-01
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPerforated AppendicitisInterventionAmpicillin, gentamicin, clindamycin, flagyl, ceftazidimePhaseNot recordedRegistry statusCompleted