Clarithromycin
FDA-approved product (tablet, oral), marketed as Biaxin, Biaxin Xl, Clarithromycin.
- Registered studies
- 50+
- Lab records
- 25
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Bacterial disease
- Chronic bronchitis
- Duodenal ulcer
- Infection
- Maxillary sinusitis
- Otitis media
- Pharyngitis
- Pneumonia
- Recurrent tonsillitis
- Sinusitis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Macrolides
- FDA pharmacologic class
- Macrolide Antimicrobial FDA label ↗
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J01FA09
Repurposing investigation
Clarithromycin 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- MRSA66.9% 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. coli63.0% 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.
- K. pneumoniae75.9% 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. tuberculosis75.2% 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.
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 10 of 12 lab records
- E. coli: measured active in 2 of 4 lab records
- K. pneumoniae: measured active in 7 of 7 lab records
- M. tuberculosis: measured active in 1 of 2 lab records
Show the 25 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 Clarithromycin 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.
- PlecanatideExisting use: Constipation52.2% AI-predicted activityagainst K. pneumoniae15 registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma51.3% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome50.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Terlipressin AcetateExisting use: Hepatorenal syndrome, Kidney failure, Renal insufficiency49.5% AI-predicted activityagainst K. pneumoniae7 registered studies
- LetermovirExisting use: Cytomegalovirus infection, Infection, Viral disease49.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Codeine SulfateExisting use: Cough, Drug dependence, Migraine disorder and 2 more48.8% AI-predicted activityagainst K. pneumoniae23 registered studies
- Bromocriptine MesylateExisting use: Acromegaly, Adenoma, Hyperprolactinemia and 4 more48.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- PimecrolimusExisting use: Atopic eczema, Eczematoid dermatitis48.3% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LypressinExisting use: Vasopressin and analogues48.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Degarelix AcetateExisting use: Prostate adenocarcinoma, Prostate cancer, Prostate carcinoma48.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more48.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Dolutegravir SodiumExisting use: HIV infection, HIV-1 infection47.9% AI-predicted activityagainst K. pneumoniae50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Clarithromycin Mechanisms in Hypersomnia Syndromes
NCT04026958 · start 2019-09-04
Registered record
- Registry ID
- NCT04026958
- Conditions
- Narcolepsy Without Cataplexy; Idiopathic Hypersomnia; Narcolepsy With Cataplexy
- Interventions
- Clarithromycin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2019-09-04
- Completion
- 2025-06-18
- Enrolment
- 83
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNarcolepsy Without Cataplexy; Idiopathic Hypersomnia; Narcolepsy With CataplexyInterventionClarithromycin; PlaceboPhasePhase 2Registry statusCompletedEmpirical vs Tailored Therapy for H. Pylori Infection
NCT04006340 · start 2019-01-04
Registered record
- Registry ID
- NCT04006340
- Conditions
- Helicobacter Pylori 23S rRNA Clarithromycin Resistance Mutation; Helicobacter Pylori Infection
- Interventions
- triple therapy; quadruple therapy; dual-priming oligonucleotide-based multiplex (DPO)-PCR test
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2019-01-04
- Completion
- 2019-08-31
- Enrolment
- 62
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter Pylori 23S rRNA Clarithromycin Resistance Mutation; Helicobacter Pylori InfectionInterventiontriple therapy; quadruple therapy; dual-priming oligonucleotide-based multiplex (DPO)-PCR testPhaseNot applicableRegistry statusUnknownDaily Four Times or Two Times Usage of PPI and Amoxicillin for the First or Second Line H. Pylori Eradication
NCT03802318 · start 2019-01-02
Registered record
- Registry ID
- NCT03802318
- Conditions
- Helicobacter Pylori Infection; Helicobacter Gastritis; Helicobacter-Associated Pyloric Ulcer
- Interventions
- Rabeprazole
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2019-01-02
- Completion
- 2020-12
- Enrolment
- 530
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter Pylori Infection; Helicobacter Gastritis; Helicobacter-Associated Pyloric UlcerInterventionRabeprazolePhaseNot applicableRegistry statusUnknownAntimicrobial Susceptibility Testing Guided Therapy Versus Empirical Therapy for the Rescue Treatment of Helicobacter Pylori Infection
NCT03565484 · start 2019-01-01
Registered record
- Registry ID
- NCT03565484
- Conditions
- Helicobacter Pylori Infection
- Interventions
- susceptibility guided therapy; personal medication history guided therapy; salvage treatment for failed eradication
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2019-01-01
- Completion
- 2020-06-30
- Enrolment
- 400
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter Pylori InfectionInterventionsusceptibility guided therapy; personal medication history guided therapy; salvage treatment for failed eradicationPhasePhase 4Registry statusUnknownProbiotics in the Reduction of Adverse Effects and Dysbiosis of H. Pylori Eradication
NCT03722433 · start 2018-08-29
Registered record
- Registry ID
- NCT03722433
- Conditions
- Helicobacter Pylori Infection
- Interventions
- Vigiis 101-LAB and sequential therapy; Placebo and sequential therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2018-08-29
- Completion
- 2020-07-31
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter Pylori InfectionInterventionVigiis 101-LAB and sequential therapy; Placebo and sequential therapyPhasePhase 4Registry statusUnknownADDITION OF BISMUTH TO THE STANDARD TRIPLE THERAPY FOR HELICOBACTER PYLORI ERADICATION
NCT03968302 · start 2018-06-01
Registered record
- Registry ID
- NCT03968302
- Conditions
- Helicobacter Pylori Infection
- Interventions
- ARM A Triple therapy for helicobacter pylori; ARM B Quadruple therapy for helicobacter pylori
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2018-06-01
- Completion
- 2019-05-15
- Enrolment
- 196
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter Pylori InfectionInterventionARM A Triple therapy for helicobacter pylori; ARM B Quadruple therapy for helicobacter pyloriPhasePhase 2Registry statusCompletedS. Aureus Decolonization in HPN Patients.
NCT03173053 · start 2018-02-08
Registered record
- Registry ID
- NCT03173053
- Conditions
- Staphylococcus Aureus; Motility Disorder
- Interventions
- Doxycycline; Trimethoprim; Sulfamethoxazole/trimethoprim; Clindamycin; Clarithromycin; Ciprofloxacin; Fusidic Acid; Rifampin; Chlorhexidine; Mupirocin; Betadine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Terminated
- Start
- 2018-02-08
- Completion
- 2021-10-14
- Enrolment
- 63
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStaphylococcus Aureus; Motility DisorderInterventionDoxycycline; Trimethoprim; Sulfamethoxazole/trimethoprim; Clindamycin +7 morePhaseNot applicableRegistry statusTerminatedBenefit of Clarithromycin in Patients With Severe Infections Through Modulation of the Immune System
NCT03345992 · start 2017-12-15
Registered record
- Registry ID
- NCT03345992
- Conditions
- Sepsis; Pneumonia; Gram-Negative Bacteria Infection; Multiple Organ Failure; Respiratory Distress Syndrome; Mortality; Biomarkers
- Interventions
- Clarithromycin; Water for injection
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2017-12-15
- Completion
- 2020-12-19
- Enrolment
- 110
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSepsis; Pneumonia; Gram-Negative Bacteria Infection; Multiple Organ Failure +3 moreInterventionClarithromycin; Water for injectionPhasePhase 3Registry statusCompletedStudy of BiRd Regimen Combined With BCMA CAR T-cell Therapy in Newly Diagnosed Multiple Myeloma (MM) Patients
NCT04287660 · start 2017-10-19
Registered record
- Registry ID
- NCT04287660
- Conditions
- Multiple Myeloma
- Interventions
- clarithromycin, lenalidomide, dexamethasone and autologous BCMA-directed CAR T-cells
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2017-10-19
- Completion
- 2025-01-31
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultiple MyelomaInterventionclarithromycin, lenalidomide, dexamethasone and autologous BCMA-directed CAR T-cellsPhasePhase 3Registry statusUnknownH. Pylori Eradication for Moderate ITP
NCT03177629 · start 2017-05-23
Registered record
- Registry ID
- NCT03177629
- Conditions
- Immune Thrombocytopenic Purpura; Helicobacter Pylori; Immune Thrombocytopenia
- Interventions
- treatment : H. pylori eradication
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2017-05-23
- Completion
- 2020-12
- Enrolment
- 54
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionImmune Thrombocytopenic Purpura; Helicobacter Pylori; Immune ThrombocytopeniaInterventiontreatment : H. pylori eradicationPhasePhase 3Registry statusUnknownAntimicrobial Susceptibility Testing Guided Antibiotic Selection Strategies in Salvage Helicobacter Pylori Treatment
NCT02988089 · start 2017-04-20
Registered record
- Registry ID
- NCT02988089
- Conditions
- Helicobacter Pylori Infection; Antimicrobial Susceptibility Testing
- Interventions
- Clarithromycin susceptibility dependant strategy; 2 susceptible antibiotics (amoxicillin, clarithromycin, metronidazole, tinidazole,levofloxacin, furazolidone and tetracycline ); proton pump inhibitor (PPI) and Colloidal Bismuth Pectin; amoxicillin and clarithromycin or amoxicillin and furazolidone; amoxicillin and furazolidone or amoxicillin and tetracycline; amoxicillin and furazolidone or amoxicillin and Tinidazole or amoxicillin and Levofloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2017-04-20
- Completion
- 2017-09
- Enrolment
- 480
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter Pylori Infection; Antimicrobial Susceptibility TestingInterventionClarithromycin susceptibility dependant strategy; 2 susceptible antibiotics (amoxicillin, clarithromycin, metronidazole, tinidazole,levofloxacin, furazolidone and tetracycline ); proton pump inhibitor (PPI) and Colloidal Bismuth Pectin; amoxicillin and clarithromycin or amoxicillin and furazolidone +2 morePhasePhase 4Registry statusUnknownCohorts of Docetaxel or Cabazitaxel in Combination With the Potent CYP3A4 Inhibitor, Clarithromycin
NCT03043989 · start 2017-03-21
Registered record
- Registry ID
- NCT03043989
- Conditions
- Prostate Cancer
- Interventions
- Docetaxel; Cabazitaxel; Clarithromycin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Terminated
- Start
- 2017-03-21
- Completion
- 2019-07-26
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionProstate CancerInterventionDocetaxel; Cabazitaxel; ClarithromycinPhasePhase 1Registry statusTerminatedClarithromycin,Lenalidomide and Dexamethasone for Relapsed/Refractory Myeloma
NCT02986451 · start 2016-12
Registered record
- Registry ID
- NCT02986451
- Conditions
- Relapse/Refractory Multiple Myeloma
- Interventions
- clarithromycin; Lenalidomide; Dexamethasone
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2016-12
- Completion
- 2019-12
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRelapse/Refractory Multiple MyelomaInterventionclarithromycin; Lenalidomide; DexamethasonePhasePhase 2Registry statusWithdrawnStudy to Evaluate Pharmacokinetic Drug Interactions and Safety of Clarithromycin, Amoxicillin and Ilaprazole
NCT02998437 · start 2016-12
Registered record
- Registry ID
- NCT02998437
- Conditions
- Drug Interaction Potentiation
- Interventions
- Ilaprazole 10mg; Clarithromycin 500mg; Amoxicillin 500 Mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2016-12
- Completion
- 2017-01
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug Interaction PotentiationInterventionIlaprazole 10mg; Clarithromycin 500mg; Amoxicillin 500 MgPhasePhase 1Registry statusCompletedSymptom Assessment for Patients With Gastro-esophageal Reflux Disease Receiving Helicobacter Pylori Eradication
NCT02934152 · start 2016-10
Registered record
- Registry ID
- NCT02934152
- Conditions
- Gastroesophageal Reflux Disease
- Interventions
- H pylori eradication; H pylori eradication timing
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2016-10
- Completion
- 2019-09
- Enrolment
- 400
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastroesophageal Reflux DiseaseInterventionH pylori eradication; H pylori eradication timingPhasePhase 4Registry statusUnknown