Rifampin
FDA-approved product (capsule, oral), marketed as Rifadin, Rifampin, Rimactane.
- Registered studies
- 50+
- Lab records
- 242
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Pulmonary tuberculosis
- Tuberculosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antibiotics
- FDA pharmacologic class
- Rifamycin Antibacterial FDA label ↗
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J04AB02; FDA class Rifamycin Antibacterial
Repurposing investigation
Rifampin 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- MRSA>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.
- E. coli88.1% 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.
- K. pneumoniae74.4% 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.
- M. tuberculosis96.4% 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.
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 3 of 3 lab records
- E. coli: measured active in 4 of 4 lab records
- K. pneumoniae: measured active in 16 of 19 lab records
- M. tuberculosis: measured active in 207 of 216 lab records
Show the latest 150 of 242 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 Rifampin 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.
Effects of Rifampin on the Pharmacokinetics of Ataluren
NCT02409004 · start 2015-02
Registered record
- Registry ID
- NCT02409004
- Conditions
- Healthy
- Interventions
- Ataluren; Rifampin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-02
- Completion
- 2015-03
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionAtaluren; RifampinPhasePhase 1Registry statusCompletedA Pharmacokinetics (PK) Study of the Effects Rabeprazole and Rifampin on Dabrafenib in Subjects With BRAF V600 Mutation Positive Tumors
NCT01954043 · start 2013-12-20
Registered record
- Registry ID
- NCT01954043
- Conditions
- Cancer
- Interventions
- Dabrafenib 150 mg twice a day (BID); Rabeprazole 40 mg once daily (OD); Rifampin 600 mg OD
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-12-20
- Completion
- 2016-02-29
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCancerInterventionDabrafenib 150 mg twice a day (BID); Rabeprazole 40 mg once daily (OD); Rifampin 600 mg ODPhasePhase 1Registry statusCompletedA Study of Baricitinib and Rifampicin in Healthy Participants
NCT01910311 · start 2013-08
Registered record
- Registry ID
- NCT01910311
- Conditions
- Healthy Volunteers
- Interventions
- Baricitinib; Rifampicin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-08
- Completion
- 2013-10
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteersInterventionBaricitinib; RifampicinPhasePhase 1Registry statusCompletedSafety, Tolerability and Pharmacokinetic (PK) of Concomitant Esomeprazole and Rifampin, and QT Study on Single and Multiple-doses of Alisertib
NCT01844583 · start 2013-06-25
Registered record
- Registry ID
- NCT01844583
- Conditions
- Solid Tumors; Lymphoma
- Interventions
- Alisertib; Esomeprazole; Rifampin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2013-06-25
- Completion
- 2016-09-06
- Enrolment
- 55
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSolid Tumors; LymphomaInterventionAlisertib; Esomeprazole; RifampinPhasePhase 1Registry statusCompletedEvaluation of Xpert MTB/RIF Assay for the Rapid Identification of TB and TB Rifampin Resistance in Pulmonary Tuberculosis Suspects
NCT01587469 · start 2012-05
Registered record
- Registry ID
- NCT01587469
- Conditions
- Tuberculosis
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2012-05
- Completion
- 2014-02-21
- Enrolment
- 992
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosisInterventionNot recordedPhaseNot recordedRegistry statusCompletedPharmacokinetics Study of Oral IXAZOMIB in Participants With Advanced Nonhematologic Malignancies or Lymphoma
NCT01454076 · start 2011-11-10
Registered record
- Registry ID
- NCT01454076
- Conditions
- Nonhematologic Malignancies; Lymphoma
- Interventions
- Ixazomib 2.5 mg; Ixazomib 4 mg Capsule A; Ixazomib 4 mg Capsule B; Ketoconazole; Rifampin; Clarithromycin; Ixazomib 4 mg Capsule B
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-11-10
- Completion
- 2016-06-16
- Enrolment
- 112
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNonhematologic Malignancies; LymphomaInterventionIxazomib 2.5 mg; Ixazomib 4 mg Capsule A; Ixazomib 4 mg Capsule B; Ketoconazole +3 morePhasePhase 1Registry statusCompletedA Drug-Drug Interaction Study of Ketoconazole, Rifampicin and Ritonavir-Boosted Atazanavir With Single-Dose RO5093151 in Healthy Volunteers
NCT01591850 · start 2011-09
Registered record
- Registry ID
- NCT01591850
- Conditions
- Healthy Volunteer
- Interventions
- RO5093151; atazanavir; ketoconazole; rifampicin; ritonavir
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-09
- Completion
- 2011-11
- Enrolment
- 51
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy VolunteerInterventionRO5093151; atazanavir; ketoconazole; rifampicin +1 morePhasePhase 1Registry statusCompletedPNU-100480 In Newly Diagnosed, Drug Sensitive Patients With Pulmonary TB; Early Bactericidal Activity; Whole Blood Assay
NCT01225640 · start 2011-08
Registered record
- Registry ID
- NCT01225640
- Conditions
- Tuberculosis
- Interventions
- PNU-100480; PNU-100480; RHZE
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2011-08
- Completion
- 2011-12
- Enrolment
- 59
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosisInterventionPNU-100480; PNU-100480; RHZEPhasePhase 2Registry statusCompletedPharmacokinetics and Pharmacodynamics of High Versus Standard Dose Rifampicin in Patients With Pulmonary Tuberculosis
NCT00760149 · start 2010-07
Registered record
- Registry ID
- NCT00760149
- Conditions
- Tuberculosis
- Interventions
- Rifampicin in higher doses
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2010-07
- Completion
- 2013-09
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosisInterventionRifampicin in higher dosesPhasePhase 2Registry statusCompletedEstimation Of Effect Of Rifampin On Pharmacokinetics Of Crizotinib In Healthy Volunteers
NCT01147055 · start 2010-07
Registered record
- Registry ID
- NCT01147055
- Conditions
- Healthy
- Interventions
- crizotinib; rifampin; crizotinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2010-07
- Completion
- 2010-10
- Enrolment
- 15
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventioncrizotinib; rifampin; crizotinibPhasePhase 1Registry statusCompletedColistin Plus Rifampicin in MDR P. Aeruginosa and A. Baumanii
NCT01297855 · start 2010-06
Registered record
- Registry ID
- NCT01297855
- Conditions
- Drug Safety
- Interventions
- Colistin; Colistin plus Rifampicin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2010-06
- Completion
- 2012-08
- Enrolment
- 130
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug SafetyInterventionColistin; Colistin plus RifampicinPhasePhase 3Registry statusUnknownTrial Comparing Efficacy of Treatments for Hidradenitis Suppurativa
NCT01063270 · start 2010-02
Registered record
- Registry ID
- NCT01063270
- Conditions
- Hidradenitis Suppurativa
- Interventions
- Clindamycin & Rifampin; Clindamycin + Rifampin along with NdYag Laser treatment
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2010-02
- Completion
- 2013-12
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHidradenitis SuppurativaInterventionClindamycin & Rifampin; Clindamycin + Rifampin along with NdYag Laser treatmentPhaseNot applicableRegistry statusCompletedStudy Evaluating The Potential Effect Of Rifampin On The Pharmacokinetics Of Neratinib
NCT00864487 · start 2009-04
Registered record
- Registry ID
- NCT00864487
- Conditions
- Healthy Subjects
- Interventions
- Neratinib
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-04
- Completion
- 2009-05
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy SubjectsInterventionNeratinibPhasePhase 1Registry statusCompletedInfluence of Drug-drug Interactions on the Pharmacokinetics (PK) of Voriconazole
NCT01080651 · start 2008-12
Registered record
- Registry ID
- NCT01080651
- Conditions
- Invasive Aspergillosis
- Interventions
- Voriconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2008-12
- Completion
- 2009-03
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInvasive AspergillosisInterventionVoriconazolePhasePhase 1Registry statusCompletedNevirapine Drug Levels in HIV Positive Patients Also Receiving Rifampicin for Tuberculosis
NCT00617643 · start 2008-05
Registered record
- Registry ID
- NCT00617643
- Conditions
- HIV Infections; Tuberculosis
- Interventions
- Nevirapine without dose escalation; Nevirapine initiation with dose escalation
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-05
- Completion
- 2010-12
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Infections; TuberculosisInterventionNevirapine without dose escalation; Nevirapine initiation with dose escalationPhasePhase 4Registry statusCompleted