Niclosamide
FDA-approved product (tablet, chewable, oral), marketed as Niclocide.
- Registered studies
- 35
- Lab records
- 4
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Helminthiasis
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Salicylic acid derivatives
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC P02DA01
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA48.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli20.1% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae6.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis47.9% 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
35registered studies name this medicine, for any condition. See them below.
Experimental
- M. tuberculosis: measured active in 4 of 4 lab records
Show the 4 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 measuredEnoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
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 Niclosamide 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.
- Trimetrexate GlucuronateExisting use: Other agents against amoebiasis and other protozoal diseases88.6% AI-predicted activityagainst E. coliLab records exist17 registered studies
- Folic AcidExisting use: Acne, Anemia, Anemia (phenotype) and 8 more87.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- MethotrexateExisting use: Acute lymphoblastic leukemia, Adenoma, Arthritis and 21 more86.8% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- PralatrexateExisting use: Cancer, Mature T-cell and NK-cell non-Hodgkin lymphoma, Neoplasm and 2 more82.2% AI-predicted activityagainst E. coli44 registered studies
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives81.0% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Leucovorin CalciumExisting use: Osteosarcoma67.6% AI-predicted activityagainst E. coli50+ registered studies
- LevoleucovorinExisting use: Anemia, Colorectal adenocarcinoma, Colorectal cancer and 3 more67.6% AI-predicted activityagainst E. coli50+ registered studies
- PyrimethamineExisting use: Malaria, Toxoplasmosis64.6% AI-predicted activityagainst E. coliLab records exist50+ registered studies
- Copanlisib DihydrochlorideExisting use: Follicular lymphoma, Neoplasm, Neoplasm of mature B-cells63.5% AI-predicted activityagainst E. coli10 registered studies
- AfamelanotideExisting use: Erythropoietic protoporphyria62.6% AI-predicted activityagainst E. coli23 registered studies
- Rimegepant SulfateExisting use: Migraine disorder61.6% AI-predicted activityagainst E. coli50+ registered studies
- Histrelin AcetateExisting use: Neoplasm, Prostate adenocarcinoma, Prostate cancer61.6% AI-predicted activityagainst E. coli13 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Safety, Tolerability, and Efficacy of CP-PCA07 in Combination With Enzalutamide in Patients With Castration-Resistant Prostate Cancer
NCT07683013 · start 2026-07
Registered record
- Registry ID
- NCT07683013
- Conditions
- Castration-Resistant Prostate Cancer (CRPC)
- Interventions
- CP-PCA07; Enzalutamide 40 mg capsule
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Not yet recruiting
- Start
- 2026-07
- Completion
- 2027-12
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCastration-Resistant Prostate Cancer (CRPC)InterventionCP-PCA07; Enzalutamide 40 mg capsulePhasePhase 1Registry statusNot yet recruitingNiclosamide in Pediatric Patients With Relapsed and Refractory AML
NCT05188170 · start 2022-11-21
Registered record
- Registry ID
- NCT05188170
- Conditions
- Acute Myeloid Leukemia (AML)
- Interventions
- Niclosamide
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Recruiting
- Start
- 2022-11-21
- Completion
- 2026-12
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Myeloid Leukemia (AML)InterventionNiclosamidePhasePhase 1Registry statusRecruitingClinical Trials to Assess Safety and Efficacy of DWRX2003 Combination With Remdesivir in Moderate to Severe COVID-19 Patients.
NCT05226533 · start 2022-03-31
Registered record
- Registry ID
- NCT05226533
- Conditions
- COVID-19
- Interventions
- DWRX2003; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2022-03-31
- Completion
- 2022-12-21
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionDWRX2003; PlaceboPhasePhase 2Registry statusTerminatedNiclosamide In Moderate COVID-19
NCT04436458 · start 2022-01-20
Registered record
- Registry ID
- NCT04436458
- Conditions
- COVID
- Interventions
- Niclosamide Oral Tablet; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2022-01-20
- Completion
- 2022-01-20
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVIDInterventionNiclosamide Oral Tablet; PlaceboPhasePhase 2Registry statusWithdrawnNiclosamide in COVID-19
NCT04542434 · start 2022-01-20
Registered record
- Registry ID
- NCT04542434
- Conditions
- Covid19
- Interventions
- Niclosamide Oral Tablet; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2022-01-20
- Completion
- 2022-01-20
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionNiclosamide Oral Tablet; PlaceboPhasePhase 2Registry statusWithdrawnSingle Ascending Dose and Multiple Ascending Dose Study of Niclosamide Inhalation Powder in Healthy Adult Subjects
NCT05168644 · start 2021-11-14
Registered record
- Registry ID
- NCT05168644
- Conditions
- Healthy
- Interventions
- Niclosamide Inhalation Powder; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2021-11-14
- Completion
- 2022-01-26
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionNiclosamide Inhalation Powder; PlaceboPhasePhase 1Registry statusCompletedRandomized-controlled Trial of the Effectiveness of COVID-19 Early Treatment in Community
NCT05087381 · start 2021-10-01
Registered record
- Registry ID
- NCT05087381
- Conditions
- Treatment Efficacy
- Interventions
- FluvoxaMINE Maleate 50 MG; Fluvoxamine, Bromhexine; Fluvoxamine, Cyproheptadine; Niclosamide Pill; Niclosamide, Bromhexine
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2021-10-01
- Completion
- 2022-06-21
- Enrolment
- 1,200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTreatment EfficacyInterventionFluvoxaMINE Maleate 50 MG; Fluvoxamine, Bromhexine; Fluvoxamine, Cyproheptadine; Niclosamide Pill +1 morePhasePhase 4Registry statusCompletedSafety and Efficacy of Intranasal Administration of Niclosamide (UNI91103) in Adults With Asymptomatic or Mild COVID-19
NCT04932915 · start 2021-09-03
Registered record
- Registry ID
- NCT04932915
- Conditions
- Covid19
- Interventions
- Niclosamide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2021-09-03
- Completion
- 2022-01-10
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionNiclosamide; PlaceboPhasePhase 2Registry statusTerminatedSafety and Efficacy of Niclosamide in Patients With COVID-19 With Gastrointestinal Infection
NCT04858425 · start 2021-04-30
Registered record
- Registry ID
- NCT04858425
- Conditions
- Covid19
- Interventions
- Niclosamide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2021-04-30
- Completion
- 2023-09-10
- Enrolment
- 166
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionNiclosamide; PlaceboPhasePhase 2Registry statusTerminatedPROphylaxis for paTiEnts at Risk of COVID-19 infecTion -V
NCT04870333 · start 2021-02-19
Registered record
- Registry ID
- NCT04870333
- Conditions
- Covid19
- Interventions
- Niclosamide; Placebo; Ciclesonide; Placebo; Sotrovimab; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2021-02-19
- Completion
- 2025-04-16
- Enrolment
- 2,240
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionNiclosamide; Placebo; Ciclesonide; Placebo +2 morePhasePhase 2 / Phase 3Registry statusCompletedSafety and Preliminary Efficacy of the Combination of Niclosamide and Camostat
NCT04750759 · start 2021-02-03
Registered record
- Registry ID
- NCT04750759
- Conditions
- Covid19
- Interventions
- Niclosamide + Camostat; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2021-02-03
- Completion
- 2021-10-29
- Enrolment
- 4
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionNiclosamide + Camostat; PlaceboPhasePhase 2Registry statusTerminatedEffectiveness of Niclosamide as Add-on Therapy to the Standard of Care Measures in COVID-19 Management
NCT04753619 · start 2021-01-03
Registered record
- Registry ID
- NCT04753619
- Conditions
- Covid-19; SARS Pneumonia
- Interventions
- Niclosamide Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2021-01-03
- Completion
- 2021-12-03
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid-19; SARS PneumoniaInterventionNiclosamide Oral TabletPhasePhase 2Registry statusUnknownTo Evaluate Safety, Tolerability and Pharmacodynamics of DWRX2003 Against COVID-19 (in Philippines)
NCT04541485 · start 2020-12-04
Registered record
- Registry ID
- NCT04541485
- Conditions
- COVID-19 Patients
- Interventions
- DWRX2003; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Terminated
- Start
- 2020-12-04
- Completion
- 2021-03-23
- Enrolment
- 2
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19 PatientsInterventionDWRX2003; PlaceboPhasePhase 1Registry statusTerminatedTo Assess the Safety, Tolerability and Pharmacokinetic Properties of Niclosamide Injectable (DWRX2003) Which is the Treatment of COVID-19 in Healthy Volunteers.
NCT04749173 · start 2020-11-21
Registered record
- Registry ID
- NCT04749173
- Conditions
- Covid19
- Interventions
- DWRX2003, 96mg; DWRX2003, 432mg; DWRX2003, 144mg; DWRX2003, 144mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2020-11-21
- Completion
- 2021-06-18
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionDWRX2003, 96mg; DWRX2003, 432mg; DWRX2003, 144mg; DWRX2003, 144mgPhasePhase 1Registry statusCompletedA Single and Multiple Ascending Dose Study of Niclosamide in Healthy Volunteers
NCT04705415 · start 2020-11-17
Registered record
- Registry ID
- NCT04705415
- Conditions
- Healthy
- Interventions
- Niclosamide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2020-11-17
- Completion
- 2022-10-28
- Enrolment
- 54
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionNiclosamide; PlaceboPhasePhase 1Registry statusCompleted