Rifamycin Sodium
FDA-approved product (tablet, delayed release, oral), marketed as Aemcolo.
- Registered studies
- 43
- Lab records
- 6
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Diarrhea
- Eye infection
- Tuberculosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antibiotics; Other antibiotics for topical use; Antiinfectives
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J04AB03; WHO ATC A07AA13; WHO ATC D06AX15; WHO ATC S01AA16
Repurposing investigation
Rifamycin 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- MRSA96.8% 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. coli74.1% 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. pneumoniae16.4% 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. tuberculosis93.6% 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
43registered studies name this medicine, for any condition. See them below.
Experimental
- MRSA: measured active in 2 of 2 lab records
- E. coli: measured active in 1 of 2 lab records
- K. pneumoniae: measured active in 0 of 1 lab record
- M. tuberculosis: measured active in 1 of 1 lab record
Show the 6 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 Rifamycin 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.
- 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.
Fecal Microbiota Transplantation for the Treatment of Refractory Hepatic Encephalopathy After TIPS Surgery
NCT07683936 · start 2026-06-01
Registered record
- Registry ID
- NCT07683936
- Conditions
- Hepatic Encephalopathy; Fecal Microbiota Transplantation; TIPS; Refractory Hepatic Encephalopathy
- Interventions
- Fecal Microbiota Transplantation; Rifaximin、Lactulose; Dietary Fiber Prebiotic
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Recruiting
- Start
- 2026-06-01
- Completion
- 2028-06-01
- Enrolment
- 26
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatic Encephalopathy; Fecal Microbiota Transplantation; TIPS; Refractory Hepatic EncephalopathyInterventionFecal Microbiota Transplantation; Rifaximin、Lactulose; Dietary Fiber PrebioticPhaseEarly phase 1Registry statusRecruitingEvaluation of the Outcome of Fecal Microbiota Transplantation
NCT07454408 · start 2026-03-07
Registered record
- Registry ID
- NCT07454408
- Conditions
- Hepatic Encephalopathy; Fecal Microbiota Transplantation; TIPS
- Interventions
- Fecal Microbiota Transplantation; FMT Matched Placebo; Rifaximin、Lactulose
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-03-07
- Completion
- 2028-06-30
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHepatic Encephalopathy; Fecal Microbiota Transplantation; TIPSInterventionFecal Microbiota Transplantation; FMT Matched Placebo; Rifaximin、LactulosePhasePhase 1 / Phase 2Registry statusNot yet recruitingDrug-drug Interaction Study of Rifampin and Anaprazole Sodium
NCT07330531 · start 2026-01-04
Registered record
- Registry ID
- NCT07330531
- Conditions
- Drug-drug Interaction Study
- Interventions
- Anelazol Sodium Enteric-coated Tablets; Rifampicin Capsules
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-01-04
- Completion
- 2027-07-21
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug-drug Interaction StudyInterventionAnelazol Sodium Enteric-coated Tablets; Rifampicin CapsulesPhasePhase 4Registry statusNot yet recruitingA Study to Evaluate VH4524184 Tablet Absorption, Effects of Food, and Interactions With Other Drugs in Healthy Adults
NCT07066722 · start 2025-07-07
Registered record
- Registry ID
- NCT07066722
- Conditions
- HIV Infections
- Interventions
- VH4524184; Itraconazole; Rifabutin; Phenytoin; Metformin; Digoxin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2025-07-07
- Completion
- 2025-12-17
- Enrolment
- 126
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV InfectionsInterventionVH4524184; Itraconazole; Rifabutin; Phenytoin +2 morePhasePhase 1Registry statusCompletedRifaximin and Cardiac Function in Patients with Heart Failure with Preserved Ejection Fraction
NCT06652087 · start 2024-09-02
Registered record
- Registry ID
- NCT06652087
- Conditions
- Bacterial Overgrowth Syndrome Small Bowel; Heart Failure with Preserved Ejection Fraction
- Interventions
- Rifaximin; Standard HFpEF treatment
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2024-09-02
- Completion
- 2027-09-30
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBacterial Overgrowth Syndrome Small Bowel; Heart Failure with Preserved Ejection FractionInterventionRifaximin; Standard HFpEF treatmentPhaseNot applicableRegistry statusRecruitingEvaluate Safety and Efficacy of Rifamycin SV MMX in the Treatment of Traveler's Diarrhea in Children Age 6 to 11 Years
NCT04026984 · start 2024-06
Registered record
- Registry ID
- NCT04026984
- Conditions
- Traveler's Diarrhea
- Interventions
- Rifamycin SV-MMX; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2024-06
- Completion
- 2025-12
- Enrolment
- 142
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTraveler's DiarrheaInterventionRifamycin SV-MMX; PlaceboPhasePhase 2Registry statusUnknownShort-course Rifamycin-based Regimens for Latent Tuberculosis in Patients With End-stage Kidney Disease
NCT05021731 · start 2024-04-20
Registered record
- Registry ID
- NCT05021731
- Conditions
- Latent Tuberculosis; Kidney Failure
- Interventions
- Rifampicin plus Isoniazid; Rifapentine plus Isoniazid; Rifampicin alone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2024-04-20
- Completion
- 2025-04-30
- Enrolment
- 225
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLatent Tuberculosis; Kidney FailureInterventionRifampicin plus Isoniazid; Rifapentine plus Isoniazid; Rifampicin alonePhasePhase 4Registry statusUnknownStudy to Evaluate Safety and Efficacy of Rifamycin SV MMX in Treating Traveler's Diarrhea in Children Age 12 to 17 Years
NCT04027894 · start 2024-01
Registered record
- Registry ID
- NCT04027894
- Conditions
- Traveler's Diarrhea
- Interventions
- Rifamycin SV MMX; Placebo to Rifamycin SV-MMX
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2024-01
- Completion
- 2025-12
- Enrolment
- 142
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTraveler's DiarrheaInterventionRifamycin SV MMX; Placebo to Rifamycin SV-MMXPhasePhase 2Registry statusUnknownA Drug-drug Interaction Study to Evaluate the Effect of Rifampicin on the Pharmacokinetics of Methotrexate in Elderly Subjects
NCT06108453 · start 2023-08-21
Registered record
- Registry ID
- NCT06108453
- Conditions
- Drug Interactions
- Interventions
- Methotrexate Sodium; Rifampicin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2023-08-21
- Completion
- 2024-11-24
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug InteractionsInterventionMethotrexate Sodium; RifampicinPhasePhase 1Registry statusUnknownA Pragmatic Trial With Optimized Dose of Rifampicin and Moxifloxacin for the Treatment of Drug Susceptible Pulmonary Tuberculosis
NCT05575518 · start 2023-08-11
Registered record
- Registry ID
- NCT05575518
- Conditions
- Tuberculosis; Human Immunodeficiency Virus
- Interventions
- Optimised rifamycin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2023-08-11
- Completion
- 2026-03-31
- Enrolment
- 414
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis; Human Immunodeficiency VirusInterventionOptimised rifamycinPhasePhase 3Registry statusUnknownThe Safety, Completion Rate and Prevention Effect by Rifamycin-containing Regimens for Latent Tuberculosis Infection in Patients With Kidney Transplantation: a Prospective Intervention Pilot Study
NCT05588492 · start 2022-01-01
Registered record
- Registry ID
- NCT05588492
- Conditions
- Pulmonology
- Interventions
- Rifamycin-containing regimen; Rifamycin-free regimen
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2022-01-01
- Completion
- 2026-12-31
- Enrolment
- 500
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonologyInterventionRifamycin-containing regimen; Rifamycin-free regimenPhasePhase 4Registry statusRecruitingTopical Rifamycin SV for Wound Healing After Sapphire FUE Hair Transplantation
NCT07155408 · start 2021-12-02
Registered record
- Registry ID
- NCT07155408
- Conditions
- Androgenetic Alopecia; Wound Healing
- Interventions
- Povidone-Iodine 10%; Rifamycin SV Sodium
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2021-12-02
- Completion
- 2022-06-22
- Enrolment
- 70
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic Alopecia; Wound HealingInterventionPovidone-Iodine 10%; Rifamycin SV SodiumPhaseNot applicableRegistry statusCompletedFruquintinib CYP3A Inhibitor and Inducer Study
NCT04557397 · start 2020-09-02
Registered record
- Registry ID
- NCT04557397
- Conditions
- Drug Drug Interaction
- Interventions
- Fruquintinib; Itraconazole; Rifampin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2020-09-02
- Completion
- 2020-10-18
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug Drug InteractionInterventionFruquintinib; Itraconazole; RifampinPhasePhase 1Registry statusCompletedEfficacy of AEMCOLO (Rifamycin SV MMX) in the Treatment of Small Intestinal Bacterial Overgrowth (SIBO)
NCT04501380 · start 2020-06-30
Registered record
- Registry ID
- NCT04501380
- Conditions
- Small Intestinal Bacterial Overgrowth; Gastrointestinal Disease; Gastrointestinal Infection
- Interventions
- AEMCOLO (Rifamycin SV MMX)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2020-06-30
- Completion
- 2022-12-30
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSmall Intestinal Bacterial Overgrowth; Gastrointestinal Disease; Gastrointestinal InfectionInterventionAEMCOLO (Rifamycin SV MMX)PhasePhase 2Registry statusUnknownComparison of Surgery and Medicine on the Impact of Diverticulitis (COSMID) Trial
NCT04095663 · start 2019-10-01
Registered record
- Registry ID
- NCT04095663
- Conditions
- Diverticulitis
- Interventions
- Partial Colectomy; Medical Management
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Active not recruiting
- Start
- 2019-10-01
- Completion
- 2027-02-01
- Enrolment
- 255
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiverticulitisInterventionPartial Colectomy; Medical ManagementPhaseNot applicableRegistry statusActive not recruiting