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.
- UrsodiolExisting use: Biliary liver cirrhosis, Primary biliary cirrhosis69.2% AI-predicted activityagainst MRSA50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more69.2% AI-predicted activityagainst MRSA50+ registered studies
- Ganirelix AcetateExisting use: Female infertility, Positive regulation of ovulation, Reproductive Techniques, Assisted69.1% AI-predicted activityagainst MRSA50+ registered studies
- DanicopanExisting use: Acquired paroxysmal nocturnal hemoglobinuria, Hemoglobinuria, Paroxysmal, Hemolysis68.7% AI-predicted activityagainst MRSA30 registered studies
- Simeprevir SodiumExisting use: Chronic hepatitis C virus infection68.6% AI-predicted activityagainst MRSANo documented evidence found
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome68.3% AI-predicted activityagainst MRSA50+ registered studies
- Cholic AcidExisting use: Abnormality of the gastrointestinal tract, Inborn errors of metabolism, Liver disease and 1 more68.0% AI-predicted activityagainst MRSA50+ registered studies
- EptifibatideExisting use: Acute coronary syndrome, Acute myocardial infarction, Intermediate coronary syndrome and 2 more67.8% AI-predicted activityagainst MRSA35 registered studies
- AbarelixExisting use: Neoplasm67.7% AI-predicted activityagainst MRSA5 registered studies
- EverolimusExisting use: Adenoma sebaceum, Anaplastic astrocytoma, Angiomyolipoma and 18 more67.5% AI-predicted activityagainst MRSA50+ registered studies
- Paliperidone PalmitateExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.3% AI-predicted activityagainst MRSA50+ registered studies
- PaliperidoneExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Targeted Versus Standard Peri-operative Antibiotic Prophylaxis in Patients Colonized With Carbapenemase Producing Enterobacterales Undergoing Liver Transplantation
NCT07759453 · start 2026-10-01
Registered record
- Registry ID
- NCT07759453
- Conditions
- Liver Transplant; Carbapenem-resistant Enterobacterales; CRE Colonization
- Interventions
- Ceftazidime - Avibactam ( CAZ-AVI); Meropenem-Vaborbactam; Imipenem+Relebactam; Cefiderocol; Aztreonam; Eravacycline; Aztreonam-Avibactam; Amoxi Clavulanate; Piperacillin + Tazobactam; Tigecycline
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Not yet recruiting
- Start
- 2026-10-01
- Completion
- 2029-09-30
- Enrolment
- 168
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLiver Transplant; Carbapenem-resistant Enterobacterales; CRE ColonizationInterventionCeftazidime - Avibactam ( CAZ-AVI); Meropenem-Vaborbactam; Imipenem+Relebactam; Cefiderocol +6 morePhasePhase 3Registry statusNot yet recruitingSafety, Pharmacokinetics and Efficacy of BV100 Plus Low Dose Polymyxin B Plus Ceftazidime/Avibactam, or Plus Cefiderocol in Patients With Pulmonary and Extrapulmonary Infections Due to Carbapenem-resistant Acinetobacter Baumannii-calcoaceticus Complex
NCT07431307 · start 2026-07
Registered record
- Registry ID
- NCT07431307
- Conditions
- Ventilator Associated Bacterial Pneumonia (VABP); Hospital Acquired Bacterial Pneumonia (HABP); Blood Stream Infection; Meningitis, Bacterial; Ventriculitis, Infectious
- Interventions
- BV100 with 50 mg polymyxin B plus ceftazidime/avibactam; BV100 with 50 mg polymyxin B plus cefiderocol; Best Available Therapy (BAT)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-07
- Completion
- 2028-07
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionVentilator Associated Bacterial Pneumonia (VABP); Hospital Acquired Bacterial Pneumonia (HABP); Blood Stream Infection; Meningitis, Bacterial +1 moreInterventionBV100 with 50 mg polymyxin B plus ceftazidime/avibactam; BV100 with 50 mg polymyxin B plus cefiderocol; Best Available Therapy (BAT)PhasePhase 2Registry statusNot yet recruitingCefotetan Therapy for Escherichia Coli Infections
NCT07318584 · start 2026-03
Registered record
- Registry ID
- NCT07318584
- Conditions
- E Coli Infection; ESBL Producing E.Coli
- Interventions
- Cefotetan; Carbapenems; Beta Lactam Antibiotics
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-03
- Completion
- 2028-08
- Enrolment
- 84
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionE Coli Infection; ESBL Producing E.ColiInterventionCefotetan; Carbapenems; Beta Lactam AntibioticsPhasePhase 2Registry statusNot yet recruitingMicrobiological and Clinical Characteristics of Severe Infections Caused by Carbapenem-Resistant Enterobacterales
NCT07160569 · start 2025-09-01
Registered record
- Registry ID
- NCT07160569
- Conditions
- Carbapenem-Resistant Enterobacteriaceae Infection
- Interventions
- Whole Genome Sequencing (WGS), Sequence Type Analysis (ST)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2025-09-01
- Completion
- 2026-08-31
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCarbapenem-Resistant Enterobacteriaceae InfectionInterventionWhole Genome Sequencing (WGS), Sequence Type Analysis (ST)PhaseNot recordedRegistry statusNot yet recruitingOptimizing the Diagnostic Approach to Cephalosporin Allergy Testing
NCT06406114 · start 2025-05-05
Registered record
- Registry ID
- NCT06406114
- Conditions
- Drug Allergy; Cephalosporin Allergy; Drug Hypersensitivity; Antibiotic Allergy; Beta Lactam Adverse Reaction; Drug-Induced Anaphylaxis; Cephalosporin Reaction
- Interventions
- Beta-lactam antibiotic (cefazolin, cefuroxime, cefotaxime, ceftazidime, ceftriaxone, cefepime, pre-pen, penicillin G, ampicillin, and histamine) double-blind skin testing; Culprit cephalosporin (cefazolin, ceftazidime, ceftriaxone, cefepime, cephalexin, cefaclor, cefadroxil, cefuroxime, cefpodoxime, cefdinir, or cefixime) double-blind placebo-controlled drug challenge; Similar cephalosporin (cefepime, ceftriaxone, cefaclor, cephalexin, cefixime, or cefdinir) antibiotic double-blind placebo-controlled drug challenge; Dissimilar cephalosporin (ceftriaxone or cefazolin) antibiotic double-blind placebo-controlled drug challenge; Amoxicillin double-blind placebo-controlled drug challenge
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-05-05
- Completion
- 2028-12-31
- Enrolment
- 300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug Allergy; Cephalosporin Allergy; Drug Hypersensitivity; Antibiotic Allergy +3 moreInterventionBeta-lactam antibiotic (cefazolin, cefuroxime, cefotaxime, ceftazidime, ceftriaxone, cefepime, pre-pen, penicillin G, ampicillin, and histamine) double-blind skin testing; Culprit cephalosporin (cefazolin, ceftazidime, ceftriaxone, cefepime, cephalexin, cefaclor, cefadroxil, cefuroxime, cefpodoxime, cefdinir, or cefixime) double-blind placebo-controlled drug challenge; Similar cephalosporin (cefepime, ceftriaxone, cefaclor, cephalexin, cefixime, or cefdinir) antibiotic double-blind placebo-controlled drug challenge; Dissimilar cephalosporin (ceftriaxone or cefazolin) antibiotic double-blind placebo-controlled drug challenge +1 morePhasePhase 2Registry statusRecruitingCONTinuous Infusion Versus Intermittent Dosing of ceftaZidime/AVIbactam in Critically Ill Patients
NCT06811727 · start 2025-05-01
Registered record
- Registry ID
- NCT06811727
- Conditions
- Severe Infection
- Interventions
- Continuos ceftazidime/avibactam infusion; Intermitent dosing as per SMPC
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2025-05-01
- Completion
- 2027-08-01
- Enrolment
- 140
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSevere InfectionInterventionContinuos ceftazidime/avibactam infusion; Intermitent dosing as per SMPCPhasePhase 4Registry statusNot yet recruitingComparison of Two Antibiotic Regimens for the Treatment of Early Airways Infection With PA in Adults With Bronchiectasis
NCT06368804 · start 2024-09-15
Registered record
- Registry ID
- NCT06368804
- Conditions
- Bronchiectasis
- Interventions
- Antibiotic monotherapy treatment and follow-up; Antibiotic bitherapy treatment and follow-up
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2024-09-15
- Completion
- 2028-09-15
- Enrolment
- 196
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBronchiectasisInterventionAntibiotic monotherapy treatment and follow-up; Antibiotic bitherapy treatment and follow-upPhasePhase 2Registry statusRecruitingRelationship Between Different Administration Regimens of Ceftazidime/Avibactam and Clinical Outcomes
NCT06528028 · start 2024-07-01
Registered record
- Registry ID
- NCT06528028
- Conditions
- Anti-Infective Agent
- Interventions
- CAZ/AVI; CAZ/AVI
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2024-07-01
- Completion
- 2025-07-30
- Enrolment
- 140
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAnti-Infective AgentInterventionCAZ/AVI; CAZ/AVIPhasePhase 4Registry statusUnknownDrug Resistance Mechanism of Enterobacteriaceae and Its Strategies
NCT05850871 · start 2023-01-06
Registered record
- Registry ID
- NCT05850871
- Conditions
- Carbapenem-Resistant Enterobacteriaceae Infection
- Interventions
- CAZ/AVI plus Aztreonam; Conventional treatment
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2023-01-06
- Completion
- 2025-01-31
- Enrolment
- 427
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCarbapenem-Resistant Enterobacteriaceae InfectionInterventionCAZ/AVI plus Aztreonam; Conventional treatmentPhaseNot applicableRegistry statusUnknownNosocomial Infections in ECMO Patients
NCT05566665 · start 2023-01-01
Registered record
- Registry ID
- NCT05566665
- Conditions
- Acute Respiratory Distress Syndrome; Nosocomial Infection; Extracorporeal Membrane Oxygenation Complication
- Interventions
- Collection of blood and bronchoalveolar samples to study Pharmacokinetics of ceftazidime/avibactam, meropenem/varbobactam, ceftolozane/tazobactam, or cefiderocol
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2023-01-01
- Completion
- 2026-12-31
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Respiratory Distress Syndrome; Nosocomial Infection; Extracorporeal Membrane Oxygenation ComplicationInterventionCollection of blood and bronchoalveolar samples to study Pharmacokinetics of ceftazidime/avibactam, meropenem/varbobactam, ceftolozane/tazobactam, or cefiderocolPhaseNot recordedRegistry statusActive not recruitingPK/PD of Ceftazidime Avitbatan Sodium in Children With Severe Infection
NCT04961580 · start 2022-10-01
Registered record
- Registry ID
- NCT04961580
- Conditions
- Sepsis; Antibiotic Reaction
- Interventions
- Ceftazidime Avitbatan Sodium
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2022-10-01
- Completion
- 2026-12-31
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSepsis; Antibiotic ReactionInterventionCeftazidime Avitbatan SodiumPhaseNot recordedRegistry statusRecruitingThe Antibiogram and Outcomes of Antimicrobial Regimens in Microbial Keratitis: A Prospective Cohort Study
NCT05655689 · start 2021-12-31
Registered record
- Registry ID
- NCT05655689
- Conditions
- Bacterial Keratitis; Fungal Keratitis; Mixed Bacterial and Fungal Keratitis; Microbial Keratitis
- Interventions
- Moxifloxacin Ophthalmic 0.5% Ophthalmic Solution; Ceftazidime 5% + vancomycin 5%; Gentamicin 1.4% + vancomycin 5%; Natamycin 5% Oph Susp; Voriconazole 1%; Natamycin 5% + voriconazole 1%; Natamycin 5%+ ceftazidime 5% + vancomycin 5%; Voriconazole 1% + ceftazidime 5% + vancomycin 5%
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2021-12-31
- Completion
- 2023-01-01
- Enrolment
- 123
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBacterial Keratitis; Fungal Keratitis; Mixed Bacterial and Fungal Keratitis; Microbial KeratitisInterventionMoxifloxacin Ophthalmic 0.5% Ophthalmic Solution; Ceftazidime 5% + vancomycin 5%; Gentamicin 1.4% + vancomycin 5%; Natamycin 5% Oph Susp +4 morePhaseNot recordedRegistry statusCompletedEarly Versus Late Stopping of Antibiotics in Children With Cancer and High-risk Febrile Neutropenia
NCT04948463 · start 2021-11-15
Registered record
- Registry ID
- NCT04948463
- Conditions
- Febrile Neutropenia
- Interventions
- Piperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection; Amikacin Injection; Ciprofloxacin; Piperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection; Amikacin Injection; Ciprofloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2021-11-15
- Completion
- 2025-12-17
- Enrolment
- 55
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFebrile NeutropeniaInterventionPiperacillin and Tazobactam for Injection; Cefepime Injection; Ceftazidime Injection; Vancomycin Injection +8 morePhasePhase 4Registry statusCompletedStudy to Assess Efficacy and Safety of PF-06947386 in Japanese Adult Patients With Complicated Intra-abdominal Infection
NCT04927312 · start 2021-10-01
Registered record
- Registry ID
- NCT04927312
- Conditions
- Complicated Intra-abdominal Infection
- Interventions
- PF-06947386; Metronidazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2021-10-01
- Completion
- 2022-09-15
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionComplicated Intra-abdominal InfectionInterventionPF-06947386; MetronidazolePhasePhase 3Registry statusCompletedEfficacy and Safety of CAZ-AVI in the Treatment of Infections Due to Carbapenem-resistant G- Pathogens in Chinese Adults
NCT04882085 · start 2021-08-26
Registered record
- Registry ID
- NCT04882085
- Conditions
- Urinary Tract Infection; Acute Pyelonephritis; Hospital Acquired Pneumonia; Ventilator-associated Pneumonia; Bacteremia; Intra-abdominal Infection
- Interventions
- Zavicefta, Ceftazidime-Avibactam; Best Available Treatment
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2021-08-26
- Completion
- 2023-08-31
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUrinary Tract Infection; Acute Pyelonephritis; Hospital Acquired Pneumonia; Ventilator-associated Pneumonia +2 moreInterventionZavicefta, Ceftazidime-Avibactam; Best Available TreatmentPhasePhase 4Registry statusCompleted