Nitazoxanide
FDA-approved product (tablet, oral), marketed as Alinia, Nitazoxanide.
- Registered studies
- 50+
- Lab records
- 1
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Amebiasis
- Diarrhea
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other agents against amoebiasis and other protozoal diseases
- FDA pharmacologic class
- Antiprotozoal FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC P01AX11; FDA class Antiprotozoal
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA36.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli33.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae15.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis77.8% 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.
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 1 of 1 lab record
Show the 1 laboratory record, 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 Nitazoxanide 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.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Sofosbuvir/Ledipasvir and Nitazoxanide for Treatment of COVID-19
NCT04498936 · start 2020-07-15
Registered record
- Registry ID
- NCT04498936
- Conditions
- COVID
- Interventions
- Sofosbuvir and Ledipasvir; Nitazoxanide
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2020-07-15
- Completion
- 2020-10-30
- Enrolment
- 240
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVIDInterventionSofosbuvir and Ledipasvir; NitazoxanidePhasePhase 4Registry statusCompletedEfficacy and Safety of Nitazoxanide 600 mg to Treat Mild Ambulatory COVID-19 Patients
NCT04441398 · start 2020-07
Registered record
- Registry ID
- NCT04441398
- Conditions
- covid19
- Interventions
- Nitazoxanide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Withdrawn
- Start
- 2020-07
- Completion
- 2020-09
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
Conditioncovid19InterventionNitazoxanide; PlaceboPhasePhase 2 / Phase 3Registry statusWithdrawnEAT-DUTA AndroCoV Trial
NCT04729491 · start 2020-06-30
Registered record
- Registry ID
- NCT04729491
- Conditions
- Covid19
- Interventions
- Dutasteride 0.5 mg; Azithromycin; Nitazoxanide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2020-06-30
- Completion
- 2020-10-07
- Enrolment
- 138
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCovid19InterventionDutasteride 0.5 mg; Azithromycin; Nitazoxanide; PlaceboPhasePhase 2 / Phase 3Registry statusCompletedEfficacy and Safety Study of Nitazoxanide (NTX) in the Treatment of Patients With SARS-CoV-2 Virus Infection (COVID-19)
NCT04463264 · start 2020-06-26
Registered record
- Registry ID
- NCT04463264
- Conditions
- COVID-19
- Interventions
- Nitazoxanide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2020-06-26
- Completion
- 2020-12-26
- Enrolment
- 135
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionNitazoxanide; PlaceboPhasePhase 2 / Phase 3Registry statusUnknownEfficacy and Safety of Nitazoxanide for the Treatment of Hospitalized Patients With Moderate COVID-19
NCT04348409 · start 2020-05-25
Registered record
- Registry ID
- NCT04348409
- Conditions
- COVID-19
- Interventions
- Nitazoxanide Tablets; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2020-05-25
- Completion
- 2020-12-31
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionNitazoxanide Tablets; PlaceboPhaseNot applicableRegistry statusCompletedPrevention of Coronavirus Disease (COVID-19) Outbreaks With Nitazoxanide
NCT04406246 · start 2020-05-21
Registered record
- Registry ID
- NCT04406246
- Conditions
- Coronavirus Infection
- Interventions
- Nitazoxanide 500Mg Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2020-05-21
- Completion
- 2020-12-31
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronavirus InfectionInterventionNitazoxanide 500Mg Oral TabletPhasePhase 4Registry statusCompletedHydroxychloroquine and Nitazoxanide Combination Therapy for COVID-19
NCT04361318 · start 2020-05
Registered record
- Registry ID
- NCT04361318
- Conditions
- COVID-19
- Interventions
- Hydroxychloroquine plus Nitazoxanide; Standard care
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2020-05
- Completion
- 2020-12
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionHydroxychloroquine plus Nitazoxanide; Standard carePhasePhase 2 / Phase 3Registry statusUnknownTreatment of Cryptosporidiosis
NCT04103216 · start 2020-02-01
Registered record
- Registry ID
- NCT04103216
- Conditions
- Cryptosporidiosis
- Interventions
- Nitazoxanide with Lactobacillus Reuteri DSM 17938; Nitazoxanide
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2020-02-01
- Completion
- 2023-08-31
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCryptosporidiosisInterventionNitazoxanide with Lactobacillus Reuteri DSM 17938; NitazoxanidePhaseNot applicableRegistry statusCompletedNitazoxanide as a New Local Adjunctive to Nonsurgical Treatment of Moderate Periodontitis
NCT04768530 · start 2019-07-20
Registered record
- Registry ID
- NCT04768530
- Conditions
- Periodontitis
- Interventions
- Scaling and Root Planing; Nitazoxanide hydrogel
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2019-07-20
- Completion
- 2020-04-30
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPeriodontitisInterventionScaling and Root Planing; Nitazoxanide hydrogelPhasePhase 2Registry statusCompletedEfficacy and Safety of Nitazoxanide in the Treatment of Colds Due to Enterovirus/Rhinovirus Infection
NCT03605862 · start 2018-09-11
Registered record
- Registry ID
- NCT03605862
- Conditions
- Enterovirus; Rhinovirus
- Interventions
- Nitazoxanide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-09-11
- Completion
- 2019-02-04
- Enrolment
- 1,756
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEnterovirus; RhinovirusInterventionNitazoxanide; PlaceboPhasePhase 3Registry statusCompletedA Unique Regimen for Treatment of Helicobacter Pylori Infection
NCT03491995 · start 2018-04-01
Registered record
- Registry ID
- NCT03491995
- Conditions
- Helicobacter Infections
- Interventions
- Quadruple therapy; Classic treatment
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Unknown
- Start
- 2018-04-01
- Completion
- 2023-04-01
- Enrolment
- 600
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHelicobacter InfectionsInterventionQuadruple therapy; Classic treatmentPhasePhase 3Registry statusUnknownEarly Life Interventions for Childhood Growth and Development In Tanzania
NCT03268902 · start 2017-09-05
Registered record
- Registry ID
- NCT03268902
- Conditions
- Malnutrition; Stunting; Cognitive Development; Enteric Pathogens
- Interventions
- Azithromycin Oral Liquid Product; Nitazoxanide Oral Suspension; Nicotinamide; Placebos
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2017-09-05
- Completion
- 2020-03-26
- Enrolment
- 1,188
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalnutrition; Stunting; Cognitive Development; Enteric PathogensInterventionAzithromycin Oral Liquid Product; Nitazoxanide Oral Suspension; Nicotinamide; PlacebosPhasePhase 2 / Phase 3Registry statusCompletedA 14 Day Early Bactericidal Activity Study of Nitazoxanide for the Treatment of Tuberculosis
NCT02684240 · start 2016-02
Registered record
- Registry ID
- NCT02684240
- Conditions
- Tuberculosis
- Interventions
- Nitazoxanide; Control
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-02
- Completion
- 2018-04-11
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTuberculosisInterventionNitazoxanide; ControlPhasePhase 2Registry statusCompletedNitazoxanide Plus Lactulose Versus Lactulose Alone Treatment of Hepatic Encephalopathy
NCT02464124 · start 2016-01
Registered record
- Registry ID
- NCT02464124
- Conditions
- Encephalopathy, Hepatic
- Interventions
- Nitazoxanide; Lactulose
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Unknown
- Start
- 2016-01
- Completion
- 2017-12
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEncephalopathy, HepaticInterventionNitazoxanide; LactulosePhasePhase 2 / Phase 3Registry statusUnknownTrial to Evaluate the Efficacy and Safety of Nitazoxanide in the Treatment of Acute Uncomplicated Influenza
NCT02612922 · start 2015-12
Registered record
- Registry ID
- NCT02612922
- Conditions
- Influenza
- Interventions
- Nitazoxanide; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2015-12
- Completion
- 2016-09-04
- Enrolment
- 325
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfluenzaInterventionNitazoxanide; PlaceboPhasePhase 3Registry statusCompleted