Rifaximin
FDA-approved product (tablet, oral), marketed as Rifaximin, Xifaxan.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Diarrhea
- Hepatic failure
- Infection
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antibiotics; Other antibiotics for topical use
- FDA pharmacologic class
- Rifamycin Antibacterial FDA label ↗
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC A07AA11; WHO ATC D06AX11; FDA class Rifamycin Antibacterial
Repurposing investigation
Rifaximin 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- MRSA93.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli70.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae28.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis87.0% 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
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
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 Rifaximin 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.
- Mefloquine HydrochlorideExisting use: Malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria81.8% AI-predicted activityagainst M. tuberculosisLab records exist8 registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more81.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome81.2% AI-predicted activityagainst M. tuberculosis6 registered studies
- Fluphenazine DecanoateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosis4 registered studies
- Fluphenazine EnanthateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- NifurtimoxExisting use: American trypanosomiasis, Chagas disease, Leishmaniasis and 1 more78.4% AI-predicted activityagainst M. tuberculosis19 registered studies
- Fluphenazine HydrochlorideExisting use: Mental or behavioural disorder, Psychosis77.8% AI-predicted activityagainst M. tuberculosis5 registered studies
- NitazoxanideExisting use: Amebiasis, Diarrhea77.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TopiramateExisting use: Epilepsy, Lennox-Gastaut syndrome, Migraine disorder and 1 more77.4% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TrabectedinExisting use: Cancer, Dedifferentiated liposarcoma, Leiomyosarcoma and 7 more76.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Chlorpromazine HydrochlorideExisting use: Conduct disorder, Mental or behavioural disorder, Nausea and vomiting and 3 more75.0% AI-predicted activityagainst M. tuberculosis33 registered studies
- ProchlorperazineExisting use: Anxiety disorder, Nausea and vomiting, Psychosis and 1 more74.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
G-CSF in Decompensated Cirrhosis: an Open Label Trial
NCT03415698 · start 2016-07
Registered record
- Registry ID
- NCT03415698
- Conditions
- Cirrhosis, Liver
- Interventions
- G-CSF; Standard Medical Therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2016-07
- Completion
- 2018-12
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosis, LiverInterventionG-CSF; Standard Medical TherapyPhasePhase 2 / Phase 3Registry statusUnknownTreating Bacterial Overgrowth in Parkinson's Disease
NCT02470780 · start 2015-12
Registered record
- Registry ID
- NCT02470780
- Conditions
- Parkinson's Disease; Small Intestinal Bacterial Overgrowth
- Interventions
- Rifaximin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2015-12
- Completion
- 2017-08
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParkinson's Disease; Small Intestinal Bacterial OvergrowthInterventionRifaximin; PlaceboPhasePhase 2 / Phase 3Registry statusCompletedEvaluation of Adherent Invasive E. Coli Eradication in Adult Crohn Disease
NCT02620007 · start 2015-12
Registered record
- Registry ID
- NCT02620007
- Conditions
- Crohn Disease; Adherent-invasive E. Coli
- Interventions
- Ciprofloxacin; Rifaximin; Ciprofloxacin Placebo; Rifaximin Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2015-12
- Completion
- 2022-06
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCrohn Disease; Adherent-invasive E. ColiInterventionCiprofloxacin; Rifaximin; Ciprofloxacin Placebo; Rifaximin PlaceboPhasePhase 2Registry statusTerminatedTrial Evaluating Chemoprophylaxis Against Travelers' Diarrhea - Prevent TD
NCT02498301 · start 2015-11-10
Registered record
- Registry ID
- NCT02498301
- Conditions
- Travelers' Diarrhea; Functional Bowel Disorders; Reactive Arthritis
- Interventions
- Rifaximin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2015-11-10
- Completion
- 2019-12-31
- Enrolment
- 449
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTravelers' Diarrhea; Functional Bowel Disorders; Reactive ArthritisInterventionRifaximin; PlaceboPhaseNot applicableRegistry statusCompletedEffect of Administration of Rifaximin on the Portal Pressure of Patients With Liver Cirrhosis and Esophageal Varices
NCT02508623 · start 2015-07
Registered record
- Registry ID
- NCT02508623
- Conditions
- Liver Cirrhosis; Portal Hypertension
- Interventions
- Rifaximin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2015-07
- Completion
- 2017-07
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLiver Cirrhosis; Portal HypertensionInterventionRifaximin; PlaceboPhasePhase 3Registry statusUnknownFecal Microbial Transplant in Pediatric Crohn's Disease
NCT02272868 · start 2015-01
Registered record
- Registry ID
- NCT02272868
- Conditions
- Crohn's Disease
- Interventions
- Fecal Microbial transplant; Normal Saline; rifaximin+omeprazole+miralax
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Terminated
- Start
- 2015-01
- Completion
- 2016-10-01
- Enrolment
- 7
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCrohn's DiseaseInterventionFecal Microbial transplant; Normal Saline; rifaximin+omeprazole+miralaxPhasePhase 1 / Phase 2Registry statusTerminatedEffect of Goal Directed Ammonia Lowering Therapy in Acute on Chronic Liver Failure Patients With Hepatic Encephalopathy.
NCT02321371 · start 2014-10-19
Registered record
- Registry ID
- NCT02321371
- Conditions
- Acute-On-Chronic Liver Failure
- Interventions
- Lactulose + Rifaximin; Lactulose
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2014-10-19
- Completion
- 2016-01-31
- Enrolment
- 73
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute-On-Chronic Liver FailureInterventionLactulose + Rifaximin; LactulosePhaseNot applicableRegistry statusCompletedRifaximin for the Secondary Prevention of Spontaneous Bacterial Peritonitis Recurrence in Cirrhotic Patients
NCT02011841 · start 2014-01
Registered record
- Registry ID
- NCT02011841
- Conditions
- Spontaneous Bacterial Peritonitis
- Interventions
- Rifaximin; Ciprofloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Withdrawn
- Start
- 2014-01
- Completion
- 2015-12
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpontaneous Bacterial PeritonitisInterventionRifaximin; CiprofloxacinPhasePhase 3Registry statusWithdrawnComparative Study of Rifaximin Versus Norfloxacin in the Secondary Prophylaxis of Spontaneous Bacterial Peritonitis
NCT02120196 · start 2014-01
Registered record
- Registry ID
- NCT02120196
- Conditions
- Spontaneous Bacterial Peritonitis; Ascites; Liver Cirrhosis
- Interventions
- Rifaximin; Norfloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2014-01
- Completion
- 2023-12
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpontaneous Bacterial Peritonitis; Ascites; Liver CirrhosisInterventionRifaximin; NorfloxacinPhasePhase 3Registry statusUnknownTo Study the Efficacy of Bromocriptine in Patients With Hepatic/Cirrhosis Related Parkinsonism
NCT02265484 · start 2013-11
Registered record
- Registry ID
- NCT02265484
- Conditions
- Cirrhosis Related Parkinsonism
- Interventions
- Lactulose+Rifaximin +Bromocriptine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2013-11
- Completion
- 2015-01
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosis Related ParkinsonismInterventionLactulose+Rifaximin +BromocriptinePhaseNot applicableRegistry statusCompletedRifaximin Predicts the Complications of Decompensated Cirrhosis
NCT02074280 · start 2013-10
Registered record
- Registry ID
- NCT02074280
- Conditions
- Cirrhosis
- Interventions
- rifaximin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2013-10
- Completion
- 2014-12
- Enrolment
- 250
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosisInterventionrifaximinPhasePhase 4Registry statusUnknownLactulose and Glucose Breath Tests as Predictors of Clinical Benefit From Rifaximin in Irritable Bowel Syndrome
NCT01803724 · start 2013-05
Registered record
- Registry ID
- NCT01803724
- Conditions
- Irritable Bowel Syndrome
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2013-05
- Completion
- 2014-12
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIrritable Bowel SyndromeInterventionNot recordedPhaseNot recordedRegistry statusUnknownQuality of Life and Nutritional Improvements in Cirrhotic Patients
NCT01842113 · start 2013-04
Registered record
- Registry ID
- NCT01842113
- Conditions
- Liver Cirrhosis; Hepatic Encephalopathy; Portal Hypertension
- Interventions
- Rifaximin; Lactulose; Lactulose Placebo; Rifaximin Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2013-04
- Completion
- Not recorded
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLiver Cirrhosis; Hepatic Encephalopathy; Portal HypertensionInterventionRifaximin; Lactulose; Lactulose Placebo; Rifaximin PlaceboPhasePhase 4Registry statusTerminatedRole of Methane in Glycemic Control
NCT01638429 · start 2012-04
Registered record
- Registry ID
- NCT01638429
- Conditions
- Diabetes; Obesity
- Interventions
- Neomycin; Rifaximin
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2012-04
- Completion
- 2014-04
- Enrolment
- 11
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes; ObesityInterventionNeomycin; RifaximinPhaseEarly phase 1Registry statusCompletedA Clinical Study to Limit Physiologic Intestinal FDG Uptake Uptake on PET-CT Scans
NCT01542541 · start 2011-07
Registered record
- Registry ID
- NCT01542541
- Conditions
- Intestinal FDG Uptake
- Interventions
- Rifaximin
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2011-07
- Completion
- 2012-10
- Enrolment
- 68
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIntestinal FDG UptakeInterventionRifaximinPhaseNot applicableRegistry statusCompleted