Ceftriaxone Sodium
FDA-approved product (injectable, injection), marketed as Ceftriaxone, Ceftriaxone And Dextrose In Duplex Container, Ceftriaxone In Plastic Container and 3 more.
- Registered studies
- 50+
- Lab records
- 68
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Bacterial disease
- Gonorrhea
- Infection
- Infectious meningitis
- Otitis media
- Pelvic Inflammatory Disease
- Respiratory tract infectious disorder
- Sepsis
- 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 J01DD04; WHO ATC J01DD54
Repurposing investigation
Ceftriaxone 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- MRSA82.4% 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.
- 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. pneumoniae35.6% 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. tuberculosis56.0% 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 8 of 8 lab records
- E. coli: measured active in 4 of 4 lab records
- K. pneumoniae: measured active in 26 of 56 lab records
Show the 68 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 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 Ceftriaxone 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.
- 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.
A Study to Assess Beta-Lactam in the Treatment of Hospitalized Patients With Bacterial Pneumonia
NCT00111644 · start 2005-03
Registered record
- Registry ID
- NCT00111644
- Conditions
- Pneumonia, Bacterial
- Interventions
- Ceftriaxone; beta-lactam; beta-lactam
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2005-03
- Completion
- 2007-01
- Enrolment
- 302
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPneumonia, BacterialInterventionCeftriaxone; beta-lactam; beta-lactamPhasePhase 2Registry statusCompletedCeftriaxone Vs Levofloxacin on Cytokine Expression in Pneumococcal Pneumonia
NCT00429975 · start 2004-08
Registered record
- Registry ID
- NCT00429975
- Conditions
- Pneumonia, Pneumococcal
- Interventions
- levofloxacin; ceftriaxone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2004-08
- Completion
- 2005-09
- Enrolment
- 45
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPneumonia, PneumococcalInterventionlevofloxacin; ceftriaxonePhasePhase 4Registry statusTerminatedCefepime vs. Ceftriaxone to Treat Nursing Home-Acquired Pneumonia
NCT00358202 · start 2002-03
Registered record
- Registry ID
- NCT00358202
- Conditions
- Pneumonia
- Interventions
- cefepime; ceftriaxone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2002-03
- Completion
- 2006-04
- Enrolment
- 69
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPneumoniaInterventioncefepime; ceftriaxonePhasePhase 4Registry statusCompletedBrain Imaging and Retreatment Study of Persistent Lyme Disease
NCT00037479 · start 1999-12
Registered record
- Registry ID
- NCT00037479
- Conditions
- Lyme Disease; Lyme Neuroborreliosis
- Interventions
- ceftriaxone
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 1999-12
- Completion
- Not recorded
- Enrolment
- 65
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLyme Disease; Lyme NeuroborreliosisInterventionceftriaxonePhasePhase 2Registry statusCompletedVNP20009 in Treating Patients With Advanced or Metastatic Solid Tumors That Have Not Responded to Previous Therapy
NCT00004216 · start 1999-08
Registered record
- Registry ID
- NCT00004216
- Conditions
- Unspecified Adult Solid Tumor, Protocol Specific
- Interventions
- salmonella VNP20009; cefixime; ceftriaxone sodium; ciprofloxacin; trimethoprim-sulfamethoxazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 1999-08
- Completion
- 2008-01
- Enrolment
- Not recorded
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionUnspecified Adult Solid Tumor, Protocol SpecificInterventionsalmonella VNP20009; cefixime; ceftriaxone sodium; ciprofloxacin +1 morePhasePhase 1Registry statusCompleted