Rifapentine
FDA-approved product (tablet, oral), marketed as Priftin, Rifapentine.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Tuberculosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antibiotics
- FDA pharmacologic class
- Rifamycin Antimycobacterial FDA label ↗
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J04AB05; FDA class Rifamycin Antimycobacterial
Repurposing investigation
Rifapentine 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- MRSA98.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. A stereoisomer of this medicine was in the model's training data.
- E. coli76.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae60.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis95.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. A stereoisomer of this medicine was in the model's training data.
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 Rifapentine 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.
- Galantamine HydrobromideExisting use: Alzheimer disease, Dementia89.6% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- Chlorhexidine GluconateExisting use: Eye infection, Gingivitis, Infection and 2 more69.3% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives68.0% AI-predicted activityagainst K. pneumoniaeLab records exist50+ registered studies
- ElvitegravirExisting use: HIV infection, HIV-1 infection, Viral disease60.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Caspofungin AcetateExisting use: Aspergillosis, Candidemia, Candidiasis and 1 more57.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm56.8% AI-predicted activityagainst K. pneumoniae50+ registered studies
- CyclosporineExisting use: Conjunctivitis, Corneal disease, Eye disease and 6 more56.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome56.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more54.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia52.7% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Micafungin SodiumExisting use: Candidiasis52.4% AI-predicted activityagainst K. pneumoniae50+ registered studies
- VoclosporinExisting use: Immune system disease, Lupus nephritis52.2% AI-predicted activityagainst K. pneumoniae28 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Trial of Stratified Patient-Centered Treatment Regimens for Active TB (SPECTRA-TB)
NCT07595042 · start 2026-10-30
Registered record
- Registry ID
- NCT07595042
- Conditions
- Tuberculosis
- Interventions
- Isoniazid; Rifampin; Pyrazinamide; Ethambutol; Rifapentine; Moxifloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-10-30
- Completion
- 2029-10-22
- Enrolment
- 900
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosisInterventionIsoniazid; Rifampin; Pyrazinamide; Ethambutol +2 morePhasePhase 2Registry statusNot yet recruitingA Study of Daily Rifapentine Combined With Isoniazid (1HP) for Tuberculosis Prevention in Children Less Than 13 Years of Age With and Without HIV
NCT07124559 · start 2026-10-15
Registered record
- Registry ID
- NCT07124559
- Conditions
- Tuberculosis
- Interventions
- Rifapentine; Isoniazid; Dolutegravir
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-10-15
- Completion
- 2028-05-31
- Enrolment
- 144
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosisInterventionRifapentine; Isoniazid; DolutegravirPhasePhase 1 / Phase 2Registry statusNot yet recruitingRifapentine-Based Shorter Regimens for Tuberculosis and TB Infection in Kazakhstan
NCT07668479 · start 2026-07-01
Registered record
- Registry ID
- NCT07668479
- Conditions
- Tuberculosis; Tuberculosis Infection, Latent; Tuberculosis, Pulmonary, Drug Sensitive
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Not yet recruiting
- Start
- 2026-07-01
- Completion
- 2027-08
- Enrolment
- 350
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis; Tuberculosis Infection, Latent; Tuberculosis, Pulmonary, Drug SensitiveInterventionNot recordedPhaseNot recordedRegistry statusNot yet recruitingBedaquiline Roll-out Evidence in Contacts and People Living With HIV to Prevent TB
NCT06568484 · start 2026-05-08
Registered record
- Registry ID
- NCT06568484
- Conditions
- Tuberculosis, Latent
- Interventions
- Bedaquiline; Isoniazid, rifapentine; Levofloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Recruiting
- Start
- 2026-05-08
- Completion
- 2027-09
- Enrolment
- 2,530
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis, LatentInterventionBedaquiline; Isoniazid, rifapentine; LevofloxacinPhasePhase 2 / Phase 3Registry statusRecruitingWindow Prophylaxis for Pediatric Tuberculosis Prevention Trial
NCT07086820 · start 2025-10-27
Registered record
- Registry ID
- NCT07086820
- Conditions
- Tuberculosis Infection; Household Contacts; Children; Adolescent; Tuberculosis Infection, Latent; Tuberculosis
- Interventions
- Tuberculosis window prophylaxis with weekly rifapentine and isoniazid for 12 weeks; Standard of care tuberculosis prophylaxis with weekly rifapentine and isoniazid for 12 weeks
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2025-10-27
- Completion
- 2028-11
- Enrolment
- 647
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis Infection; Household Contacts; Children; Adolescent +2 moreInterventionTuberculosis window prophylaxis with weekly rifapentine and isoniazid for 12 weeks; Standard of care tuberculosis prophylaxis with weekly rifapentine and isoniazid for 12 weeksPhaseNot applicableRegistry statusRecruitingShorter and Safer Treatment Regimens for Latent TB
NCT06498414 · start 2025-06-10
Registered record
- Registry ID
- NCT06498414
- Conditions
- Tuberculosis Infection, Latent
- Interventions
- rifampin standard arm; rifampin double dose; levofloxacin and rifapentine
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Recruiting
- Start
- 2025-06-10
- Completion
- 2029-06-01
- Enrolment
- 1,800
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis Infection, LatentInterventionrifampin standard arm; rifampin double dose; levofloxacin and rifapentinePhasePhase 2 / Phase 3Registry statusRecruitingShort-Course Anti-tuberculosis Regimens for Mild Spinal Tuberculosis
NCT06917495 · start 2025-04-05
Registered record
- Registry ID
- NCT06917495
- Conditions
- Mild Spinal Tuberculosis
- Interventions
- Rifampin; Isoniazid; Rifapentine (RPT); Moxifloxacin; Pyrazinamide; Ethambutol
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2025-04-05
- Completion
- 2029-12-31
- Enrolment
- 300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMild Spinal TuberculosisInterventionRifampin; Isoniazid; Rifapentine (RPT); Moxifloxacin +2 morePhasePhase 2Registry statusNot yet recruitingShortened Regimen for Drug-susceptible TB in Children
NCT06253715 · start 2025-01-15
Registered record
- Registry ID
- NCT06253715
- Conditions
- Tuberculosis; Tuberculosis, Pulmonary; Tuberculosis, Lymph Node; Mycobacterium Tuberculosis
- Interventions
- Isoniazid; Rifampin; Pyrazinamide; Ethambutol; Rifapentine; Moxifloxacin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-01-15
- Completion
- 2027-09-30
- Enrolment
- 860
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis; Tuberculosis, Pulmonary; Tuberculosis, Lymph Node; Mycobacterium TuberculosisInterventionIsoniazid; Rifampin; Pyrazinamide; Ethambutol +2 morePhasePhase 3Registry statusRecruitingDolutegravir Pharmacokinetics During Weekly Rifapentine/Isoniazid for TB Prevention
NCT06281834 · start 2024-11-15
Registered record
- Registry ID
- NCT06281834
- Conditions
- Pediatric HIV Infection; Latent Tuberculosis
- Interventions
- Rifapentine; Dolutegravir
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Recruiting
- Start
- 2024-11-15
- Completion
- 2027-06-01
- Enrolment
- 25
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediatric HIV Infection; Latent TuberculosisInterventionRifapentine; DolutegravirPhasePhase 1Registry statusRecruitingIntroduction of Dispersible 3HP Formulations for TB Preventive Treatment in Children: a Multi-country Evaluation
NCT06511180 · start 2024-08
Registered record
- Registry ID
- NCT06511180
- Conditions
- TB - Tuberculosis; Household Contact; HIV; Children, Only
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2024-08
- Completion
- 2025-06
- Enrolment
- 1,200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTB - Tuberculosis; Household Contact; HIV; Children, OnlyInterventionNot recordedPhaseNot recordedRegistry statusUnknownBCG Revaccination in Children and Adolescents
NCT05330884 · start 2024-07-15
Registered record
- Registry ID
- NCT05330884
- Conditions
- Tuberculosis Infection; Tuberculosis
- Interventions
- BCG vaccine; Oral Chemoprophylaxis
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Suspended
- Start
- 2024-07-15
- Completion
- 2027-12
- Enrolment
- 9,200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis Infection; TuberculosisInterventionBCG vaccine; Oral ChemoprophylaxisPhasePhase 3Registry statusSuspendedShort-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 statusUnknownThiPhiSA: New Pathways to Prevention From Community TB Screening in South Africa
NCT06214910 · start 2024-02-20
Registered record
- Registry ID
- NCT06214910
- Conditions
- Tuberculosis; HIV I Infection
- Interventions
- Community-delivered TB preventive therapy (TPT) - 3 months weekly isoniazid plus rifapentine (3HP); Clinic-link TPT
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2024-02-20
- Completion
- 2025-08-04
- Enrolment
- 301
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis; HIV I InfectionInterventionCommunity-delivered TB preventive therapy (TPT) - 3 months weekly isoniazid plus rifapentine (3HP); Clinic-link TPTPhaseNot applicableRegistry statusCompletedPharmacokinetics and Safety of Double-dose Dolutegravir When Used With Rifapentine for HIV-associated Tuberculosis
NCT05630872 · start 2024-02-13
Registered record
- Registry ID
- NCT05630872
- Conditions
- HIV-associated Tuberculosis
- Interventions
- Dolutegravir (DTG) 50 mg orally BID (~12 hours apart) plus TDF/3TC; DTG 50 mg orally QD plus TDF/3TC; 2HPZM; 2HPM
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2024-02-13
- Completion
- 2025-11-12
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV-associated TuberculosisInterventionDolutegravir (DTG) 50 mg orally BID (~12 hours apart) plus TDF/3TC; DTG 50 mg orally QD plus TDF/3TC; 2HPZM; 2HPMPhasePhase 2Registry statusCompletedSafety and Tolerability of 1 Month Daily (1HP) and 3 Months Weekly (3HP) Isoniazid and Rifapentine With Pharmacokinetics of Dolutegravir (DTG) in Pregnant People With HIV
NCT05122026 · start 2024-01-17
Registered record
- Registry ID
- NCT05122026
- Conditions
- HIV Seropositivity; Pregnancy; Tuberculosis Infection
- Interventions
- Rifapentine; Isoniazid
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Active not recruiting
- Start
- 2024-01-17
- Completion
- 2025-12-31
- Enrolment
- 252
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHIV Seropositivity; Pregnancy; Tuberculosis InfectionInterventionRifapentine; IsoniazidPhasePhase 1 / Phase 2Registry statusActive not recruiting