Moxidectin
FDA-approved product (tablet, oral), marketed as Moxidectin.
- Registered studies
- 25
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Helminthiasis
- Onchocerciasis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other antinematodals
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC P02CX03
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli, K. pneumoniae 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- MRSA50.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli42.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae41.7% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis51.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
25registered studies name this medicine, for any condition. 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 Moxidectin 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.
Efficacy, Safety, and PK of Ascending Dosages of Moxidectin Versus Ivermectin Against Strongyloides Stercoralis
NCT04056325 · start 2019-11-27
Registered record
- Registry ID
- NCT04056325
- Conditions
- Strongyloides Stercoralis Infection
- Interventions
- Moxidectin; Ivermectin; Placebo oral tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2019-11-27
- Completion
- 2021-04-30
- Enrolment
- 617
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStrongyloides Stercoralis InfectionInterventionMoxidectin; Ivermectin; Placebo oral tabletPhasePhase 2 / Phase 3Registry statusCompletedEstimating the Malaria Prevention Impact of New Nets: Observational Analyses to Evaluate the Evidence Generated During Piloted New Net Distributions in Burkina Faso
NCT04157894 · start 2019-07-07
Registered record
- Registry ID
- NCT04157894
- Conditions
- Malaria
- Interventions
- Standard long-lasting insecticidal net; Chlorfenapyr insecticide treated net; Piperonyl butoxide long-lasting insecticidal net
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2019-07-07
- Completion
- 2022-07-06
- Enrolment
- 5,606
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalariaInterventionStandard long-lasting insecticidal net; Chlorfenapyr insecticide treated net; Piperonyl butoxide long-lasting insecticidal netPhaseNot recordedRegistry statusCompletedEfficacy and Safety of Ascending Dosages of Moxidectin and Moxidectin-albendazole Against Trichuris Trichiura
NCT03501251 · start 2018-07-03
Registered record
- Registry ID
- NCT03501251
- Conditions
- Trichuris Trichiura; Infection
- Interventions
- Moxidectin 8mg; Moxidectin 8 mg + albendazole 400 mg; Moxidectin 16 mg; Moxidectin 16 mg + albendazole 400 mg; Moxidectin 24 mg; Moxidectin 24 mg + albendazole 400 mg; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2018-07-03
- Completion
- 2018-08-11
- Enrolment
- 286
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTrichuris Trichiura; InfectionInterventionMoxidectin 8mg; Moxidectin 8 mg + albendazole 400 mg; Moxidectin 16 mg; Moxidectin 16 mg + albendazole 400 mg +3 morePhasePhase 2Registry statusCompletedEffect of a Single Oral Dose of Moxidectin on the Cardiac QT Interval of Healthy Volunteers
NCT03012828 · start 2017-01
Registered record
- Registry ID
- NCT03012828
- Conditions
- QT Effects in Healthy Volunteers
- Interventions
- Moxidectin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-01
- Completion
- 2017-05
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionQT Effects in Healthy VolunteersInterventionMoxidectin; PlaceboPhasePhase 1Registry statusCompletedPediatric Pharmacokinetics And Safety Study Of Moxidectin
NCT01035619 · start 2011-04
Registered record
- Registry ID
- NCT01035619
- Conditions
- Onchocerciasis
- Interventions
- moxidectin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2011-04
- Completion
- 2011-04
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOnchocerciasisInterventionmoxidectinPhasePhase 2Registry statusWithdrawnStudy Comparing Moxidectin And Ivermectin In Subjects With Onchocerca Volvulus Infection
NCT00790998 · start 2009-04
Registered record
- Registry ID
- NCT00790998
- Conditions
- Onchocerciasis
- Interventions
- Moxidectin; Ivermectin
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-04
- Completion
- 2012-05
- Enrolment
- 1,497
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOnchocerciasisInterventionMoxidectin; IvermectinPhasePhase 3Registry statusCompletedStudy Evaluating The Co-Administration Of Moxidectin And Midazolam In Healthy Subjects
NCT00856362 · start 2009-04
Registered record
- Registry ID
- NCT00856362
- Conditions
- Healthy
- Interventions
- Moxidectin; Midazolam
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2009-04
- Completion
- 2009-09
- Enrolment
- 38
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionMoxidectin; MidazolamPhasePhase 1Registry statusCompletedStudy Evaluating The Effect Of High-Fat Meal On Bioavailability And Pharmacokinetics Of Single Dose Of Moxidectin
NCT00736697 · start 2008-11
Registered record
- Registry ID
- NCT00736697
- Conditions
- Infection
- Interventions
- moxidectin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2008-11
- Completion
- 2009-05
- Enrolment
- 54
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfectionInterventionmoxidectinPhasePhase 1Registry statusCompletedStudy Evaluating The Excretion Of Moxidectin Into The Breast Milk Of Lactating, Non-Breastfeeding Women
NCT00751764 · start 2008-11
Registered record
- Registry ID
- NCT00751764
- Conditions
- Infection
- Interventions
- Moxidectin
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2008-11
- Completion
- 2009-09
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInfectionInterventionMoxidectinPhasePhase 1Registry statusCompletedStudy Evaluating Orally Administered Moxidectin In Subjects With Onchocerca Volvulus Infection
NCT00300768 · start 2006-09-06
Registered record
- Registry ID
- NCT00300768
- Conditions
- Onchocerciasis
- Interventions
- 2 mg moxidectin; ivermectin 150 mcg/kg; 4 mg moxidectin; 8 mg moxidectin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2006-09-06
- Completion
- 2009-11-29
- Enrolment
- 172
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOnchocerciasisIntervention2 mg moxidectin; ivermectin 150 mcg/kg; 4 mg moxidectin; 8 mg moxidectinPhasePhase 2Registry statusCompleted