Clofazimine
FDA-approved product (capsule, oral), marketed as Lamprene.
- Registered studies
- 50+
- Lab records
- 5
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Leprosy
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Drugs for treatment of lepra
- FDA pharmacologic class
- Antimycobacterial FDA label ↗
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J04BA01; FDA class Antimycobacterial
Repurposing investigation
Clofazimine 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- MRSA39.7% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli30.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae20.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis78.6% 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
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
- M. tuberculosis: measured active in 5 of 5 lab records
Show the 5 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 measuredAutoDock 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 Clofazimine 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.
Testing a Novel Combination Treatment (Arm D) Versus Standard of Care for Intensive Phase Treatment for Mycobacterium Abscessus Pulmonary Disease in People With or Without Cystic Fibrosis in the Finding the Optimal Regimen for Mycobacterium Abscessus Treatment (FORMaT) Adaptive Platform Trial
NCT07485010 · start 2027-04
Registered record
- Registry ID
- NCT07485010
- Conditions
- Mycobacterium Abscessus Pulmonary Disease; Mycobacterium Abscessus Infection; Non-Tuberculous Mycobacterial (NTM) Infections; Non-Tuberculous Mycobacteria Pulmonary Disease
- Interventions
- Sulbactam 25mg/kg -Durlobactam 25mg/kg (Every 6 hours); Ceftriaxone for Injection; Amoxicillin; Azithromcyin; clarithromycin; Clofazimine; Ethambutol; Amikacin Injection; tigecycline; Imipenem + Cilastatin; Cefoxitin; Amikacin (Inhalation); linezolid; Trimethoprim / Sulfamethoxazole; Doxycycline; moxifloxacin; bedaquiline; Rifabutin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2027-04
- Completion
- 2031-07
- Enrolment
- 300
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMycobacterium Abscessus Pulmonary Disease; Mycobacterium Abscessus Infection; Non-Tuberculous Mycobacterial (NTM) Infections; Non-Tuberculous Mycobacteria Pulmonary DiseaseInterventionSulbactam 25mg/kg -Durlobactam 25mg/kg (Every 6 hours); Ceftriaxone for Injection; Amoxicillin; Azithromcyin +14 morePhasePhase 2Registry statusNot yet recruitingBacteriophage Therapy for Mycobacterium Abscessus Pulmonary Infection
NCT07228702 · start 2026-01-11
Registered record
- Registry ID
- NCT07228702
- Conditions
- Non-Tuberculous Mycobacterial (NTM) Pneumonia; Mycobacterium Abscessus Infection
- Interventions
- Mycobacteriophage Muddy_HRMN0052; Amikacin Injection; Clofazimine; Bedaquiline (B); Linezolid (LZD); Sulfamethoxazole/Trimethoprim; Imipenem + Cilastatin; Ceftaroline fosamil; Omadacycline Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Enrolling by invitation
- Start
- 2026-01-11
- Completion
- 2027-10
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNon-Tuberculous Mycobacterial (NTM) Pneumonia; Mycobacterium Abscessus InfectionInterventionMycobacteriophage Muddy_HRMN0052; Amikacin Injection; Clofazimine; Bedaquiline (B) +5 morePhasePhase 1Registry statusEnrolling by invitation6 Months of Bedaquiline(BDQ), Delamanid(DLM), Linezolid(LZD) and Levofloxacin(LFX) in RR-TB Patients in Hubei Province
NCT07198685 · start 2025-09-30
Registered record
- Registry ID
- NCT07198685
- Conditions
- Treat to Target; Treatment Duration
- Interventions
- bedaquiline; Delamanid (DLM); Linezolid (LZD); Levofloxacin; Cycloserine; Clofazimine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2025-09-30
- Completion
- 2028-09-30
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTreat to Target; Treatment DurationInterventionbedaquiline; Delamanid (DLM); Linezolid (LZD); Levofloxacin +2 morePhaseNot applicableRegistry statusNot yet recruitingA Phase 2b Clinical Study of JDB0131 Benzenesulfonate Tablets
NCT07170800 · start 2025-09-19
Registered record
- Registry ID
- NCT07170800
- Conditions
- Tuberculosis; Multidrug Resistant Pulmonary Tuberculosis; Rifampicin-resistant Tuberculosis
- Interventions
- JDB0131 100mg; JDB0131 200mg; Delamanid (D)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2025-09-19
- Completion
- 2026-09-04
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis; Multidrug Resistant Pulmonary Tuberculosis; Rifampicin-resistant TuberculosisInterventionJDB0131 100mg; JDB0131 200mg; Delamanid (D)PhasePhase 2Registry statusRecruitingA Study on the Short-course Treatment Regimen Containing Pretomanid for Drug-resistant Tuberculosis
NCT07126639 · start 2025-09-01
Registered record
- Registry ID
- NCT07126639
- Conditions
- Efficacy and Safety
- Interventions
- bedaquiline; Pretomanid (Pa); linezolid; Moxifloxacin (M); Delamanid (D); Levofloxacin; clofazimine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2025-09-01
- Completion
- 2028-09-30
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEfficacy and SafetyInterventionbedaquiline; Pretomanid (Pa); linezolid; Moxifloxacin (M) +3 morePhaseNot applicableRegistry statusNot yet recruitingRab 32 Gene Polymorphisms as a Prognostic Factor in Leprosy Patients
NCT06819449 · start 2024-12-20
Registered record
- Registry ID
- NCT06819449
- Conditions
- Leprosy; Mycobacterium Leprae Infection
- Interventions
- Dapsone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2024-12-20
- Completion
- 2025-12-20
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLeprosy; Mycobacterium Leprae InfectionInterventionDapsonePhaseNot applicableRegistry statusRecruitingInnovating Shorter, All- Oral, Precised Treatment Regimen for Rifampicin Resistant Tuberculosis:BDLL Chinese Cohort
NCT06649721 · start 2024-11-27
Registered record
- Registry ID
- NCT06649721
- Conditions
- Drug-resistant Tuberculosis; Pulmonary Tuberculosis; Rifampin-resistant Tuberculosis
- Interventions
- bedaquiline; delamanid; linezolid; Levofloxacin; Clofazimine
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2024-11-27
- Completion
- 2027-06-30
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug-resistant Tuberculosis; Pulmonary Tuberculosis; Rifampin-resistant TuberculosisInterventionbedaquiline; delamanid; linezolid; Levofloxacin +1 morePhasePhase 3Registry statusActive not recruitingICoN-1 Phase 3 Study of the Efficacy and Safety of Treatment With MNKD-101, Clofazimine Inhalation Suspension
NCT06418711 · start 2024-09-11
Registered record
- Registry ID
- NCT06418711
- Conditions
- MAC Lung Disease; Treatment Refractory MAC Lung Disease; Mycobacterium Infections, Nontuberculous
- Interventions
- Clofazimine Inhalation Suspension; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2024-09-11
- Completion
- 2025-11-10
- Enrolment
- 132
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMAC Lung Disease; Treatment Refractory MAC Lung Disease; Mycobacterium Infections, NontuberculousInterventionClofazimine Inhalation Suspension; PlaceboPhasePhase 3Registry statusTerminatedInnovating Shorter, All- Oral, Precised, Individualized Treatment Regimen for Rifampicin Resistant Tuberculosis:Contezolid, Delamanid and Bedaquiline Cohort
NCT06081361 · start 2023-12-22
Registered record
- Registry ID
- NCT06081361
- Conditions
- Pulmonary Tuberculosis; Rifampicin-resistant Tuberculosis
- Interventions
- Bedaquiline; Delamanid; Contezolid; Levofloxacin; Moxifloxacin; Clofazimine; Linezolid; Cycloserine; Prothionamide; Pyrazinamide; Para-Aminosalicylic Acid; Ethambutol
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Active not recruiting
- Start
- 2023-12-22
- Completion
- 2026-12-31
- Enrolment
- 186
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPulmonary Tuberculosis; Rifampicin-resistant TuberculosisInterventionBedaquiline; Delamanid; Contezolid; Levofloxacin +8 morePhasePhase 3Registry statusActive not recruitingUltra-Short Course Bedaquiline, Clofazimine, Pyrazinamide and Delamanid Versus Standard Therapy for Drug-Susceptible Tuberculosis
NCT05556746 · start 2023-11-24
Registered record
- Registry ID
- NCT05556746
- Conditions
- Tuberculosis, Pulmonary; HIV
- Interventions
- Bedaquiline (BDQ); Clofazimine (CFZ); Pyrazinamide (PZA); Delamanid (DLM); Rifampicin (RIF); Isoniazid (INH); Ethambutol (EMB); Pyrazinamide (PZA)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Active not recruiting
- Start
- 2023-11-24
- Completion
- 2027-01
- Enrolment
- 94
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis, Pulmonary; HIVInterventionBedaquiline (BDQ); Clofazimine (CFZ); Pyrazinamide (PZA); Delamanid (DLM) +4 morePhasePhase 2Registry statusActive not recruitingLinezolid Dosing Strategies in Drug-Resistant TB
NCT05007821 · start 2022-09-27
Registered record
- Registry ID
- NCT05007821
- Conditions
- Tuberculosis, Multidrug-Resistant; Tuberculosis; Tuberculosis, Pulmonary
- Interventions
- Linezolid 600 mg; Linezolid 1200 mg (QD); Linezolid 1200 mg (TIW); Bedaquiline 200 mg; Bedaquiline 100 mg; Delamanid 300 mg; Clofazimine 300 mg; Clofazimine 100 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2022-09-27
- Completion
- 2026-01-13
- Enrolment
- 138
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis, Multidrug-Resistant; Tuberculosis; Tuberculosis, PulmonaryInterventionLinezolid 600 mg; Linezolid 1200 mg (QD); Linezolid 1200 mg (TIW); Bedaquiline 200 mg +4 morePhasePhase 2Registry statusCompletedClinical Study of New Intensive Treatment Regimen for Severe Nontuberculous Mycobacterial Pulmonary Disease
NCT05494957 · start 2022-08-05
Registered record
- Registry ID
- NCT05494957
- Conditions
- Nontuberculous Mycobacterial Lung Disease
- Interventions
- New regimen(BdqCfzLzd+XY)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2022-08-05
- Completion
- 2025-08-05
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNontuberculous Mycobacterial Lung DiseaseInterventionNew regimen(BdqCfzLzd+XY)PhasePhase 4Registry statusUnknownInnovating(IN) Shorter(S), All- Oral, Precised(P), Individualized(I) Treatment Regimen(RE) for Rifampicin Resistant Tuberculosis(INSPIRE-TB)
NCT05081401 · start 2022-05-23
Registered record
- Registry ID
- NCT05081401
- Conditions
- Multidrug Resistant Tuberculosis; Rifampicin Resistant Tuberculosis; Pre-XDR-TB
- Interventions
- Bdq(Lzd)+Lfx(Mfx)+Cfz(Cs)+Pto+E+H+Z; A1; A2a; A2b; A2c; A3; A4; A5; B-SOC; B1
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2022-05-23
- Completion
- 2027-12-01
- Enrolment
- 1,050
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMultidrug Resistant Tuberculosis; Rifampicin Resistant Tuberculosis; Pre-XDR-TBInterventionBdq(Lzd)+Lfx(Mfx)+Cfz(Cs)+Pto+E+H+Z; A1; A2a; A2b +6 morePhasePhase 3Registry statusRecruitingA Study of an Oral Short-course Regimen Including Bedaquiline for the Treatment of Participants With Multidrug-resistant Tuberculosis in China
NCT05306223 · start 2022-05-10
Registered record
- Registry ID
- NCT05306223
- Conditions
- Tuberculosis, Multidrug-Resistant
- Interventions
- Bedaquiline; Levofloxacin; Linezolid; Cycloserine; Clofazimine; Pyrazinamide; Protionamide
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2022-05-10
- Completion
- 2025-08-08
- Enrolment
- 212
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosis, Multidrug-ResistantInterventionBedaquiline; Levofloxacin; Linezolid; Cycloserine +3 morePhasePhase 4Registry statusUnknownPharmacokinetic Study With a Loading Dose of Clofazimine in Adult Patients With Nontuberculous Mycobacterial Disease
NCT05294146 · start 2022-02-14
Registered record
- Registry ID
- NCT05294146
- Conditions
- Nontuberculous Mycobacterial Diseases
- Interventions
- Clofazimine
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2022-02-14
- Completion
- 2023-08-08
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionNontuberculous Mycobacterial DiseasesInterventionClofaziminePhasePhase 2Registry statusCompleted