Amisulpride
FDA-approved product (solution, intravenous), marketed as Barhemsys.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Nausea and vomiting
- Post operative nausea and vomiting
- Psychosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Benzamides
- FDA pharmacologic class
- Dopamine-2 Receptor Antagonist FDA label ↗
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis, MRSA and E. coli. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA41.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli42.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae35.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis66.8% 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
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 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 Amisulpride 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.
- Mefloquine HydrochlorideExisting use: Malaria, Plasmodium falciparum malaria, Plasmodium vivax malaria81.8% AI-predicted activityagainst M. tuberculosisLab records exist8 registered studies
- KetoconazoleExisting use: Adrenal gland disease, Blastomycosis, Cushing syndrome and 3 more81.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- LevoketoconazoleExisting use: Adrenal gland disease, Adrenal gland hyperfunction, Cushing syndrome81.2% AI-predicted activityagainst M. tuberculosis6 registered studies
- Fluphenazine DecanoateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosis4 registered studies
- Fluphenazine EnanthateExisting use: Mental or behavioural disorder, Psychosis80.7% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- NifurtimoxExisting use: American trypanosomiasis, Chagas disease, Leishmaniasis and 1 more78.4% AI-predicted activityagainst M. tuberculosis19 registered studies
- Fluphenazine HydrochlorideExisting use: Mental or behavioural disorder, Psychosis77.8% AI-predicted activityagainst M. tuberculosis5 registered studies
- NitazoxanideExisting use: Amebiasis, Diarrhea77.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TopiramateExisting use: Epilepsy, Lennox-Gastaut syndrome, Migraine disorder and 1 more77.4% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- TrabectedinExisting use: Cancer, Dedifferentiated liposarcoma, Leiomyosarcoma and 7 more76.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Chlorpromazine HydrochlorideExisting use: Conduct disorder, Mental or behavioural disorder, Nausea and vomiting and 3 more75.0% AI-predicted activityagainst M. tuberculosis33 registered studies
- ProchlorperazineExisting use: Anxiety disorder, Nausea and vomiting, Psychosis and 1 more74.1% AI-predicted activityagainst M. tuberculosis50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Effectiveness and Safety of Amisulpride in Chinese Patients With Schizophrenia
NCT01795183 · start 2012-11
Registered record
- Registry ID
- NCT01795183
- Conditions
- Schizophrenia
- Interventions
- AMISULPRIDE
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2012-11
- Completion
- 2013-12
- Enrolment
- 316
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionAMISULPRIDEPhasePhase 4Registry statusCompletedComparison of Antipsychotic Combination Treatment of Olanzapine and Amisulpride to Monotherapy
NCT01609153 · start 2012-06
Registered record
- Registry ID
- NCT01609153
- Conditions
- Schizophrenia; Schizoaffective Disorder
- Interventions
- Olanzapine; Amisulpride; Olanzapine and Amisulpride
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2012-06
- Completion
- 2019-04
- Enrolment
- 328
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizoaffective DisorderInterventionOlanzapine; Amisulpride; Olanzapine and AmisulpridePhasePhase 4Registry statusCompletedOptimisation of Antipsychotic Drug Use in Older People
NCT01454453 · start 2012-05
Registered record
- Registry ID
- NCT01454453
- Conditions
- Alzheimer's Disease; Schizophrenia
- Interventions
- Patients- dose titration
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2012-05
- Completion
- 2015-07
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAlzheimer's Disease; SchizophreniaInterventionPatients- dose titrationPhasePhase 4Registry statusTerminatedThe Effects of Dopamine on Reward Processing
NCT01253421 · start 2012-02
Registered record
- Registry ID
- NCT01253421
- Conditions
- Major Depressive Disorder (MDD)
- Interventions
- amisulpride; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2012-02
- Completion
- 2016-05
- Enrolment
- 159
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMajor Depressive Disorder (MDD)Interventionamisulpride; placeboPhasePhase 1Registry statusCompletedAmisulpride Augmentation in Clozapine-unresponsive Schizophrenia
NCT01246232 · start 2011-09
Registered record
- Registry ID
- NCT01246232
- Conditions
- Schizophrenia
- Interventions
- Amisulpride; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2011-09
- Completion
- 2015-03
- Enrolment
- 69
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionAmisulpride; placeboPhasePhase 4Registry statusCompletedOptimization of Treatment and Management of Schizophrenia in Europe
NCT01248195 · start 2011-05
Registered record
- Registry ID
- NCT01248195
- Conditions
- Schizophrenia; Schizophreniform Disorder; Schizoaffective Disorder
- Interventions
- Amisulpride open label; 6-week amisulpride double blind treatment; 6-week olanzapine double blind treatment; 12-week clozapine open-label treatment; Psychosocial intervention
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2011-05
- Completion
- 2016-04
- Enrolment
- 479
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizophreniform Disorder; Schizoaffective DisorderInterventionAmisulpride open label; 6-week amisulpride double blind treatment; 6-week olanzapine double blind treatment; 12-week clozapine open-label treatment +1 morePhasePhase 4Registry statusCompletedInvestigation of the Safety, Tolerability and Potential Therapeutic Effects of JNJ-40411813 in Patients With Schizophrenia
NCT01323205 · start 2011-05
Registered record
- Registry ID
- NCT01323205
- Conditions
- Schizophrenia
- Interventions
- JNJ-40411813; JNJ-40411813; Placebo; Antipsychotic medication
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2011-05
- Completion
- 2012-12
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionJNJ-40411813; JNJ-40411813; Placebo; Antipsychotic medicationPhasePhase 2Registry statusCompletedOptimization of Treatment and Management of Schizophrenia in Europe (OPTIMISE): Substudy Site Copenhagen
NCT01555814 · start 2011-05
Registered record
- Registry ID
- NCT01555814
- Conditions
- Schizophrenia; Schizophreniform Disorder; Schizoaffective Disorder
- Interventions
- Amisulpride
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2011-05
- Completion
- 2016-10
- Enrolment
- 56
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizophreniform Disorder; Schizoaffective DisorderInterventionAmisulpridePhaseNot applicableRegistry statusCompletedEfficacy of an Early Antipsychotic Switch in Case of Poor Initial Response to the Treatment of Schizophrenia
NCT01029769 · start 2009-12
Registered record
- Registry ID
- NCT01029769
- Conditions
- Schizophrenia; Schizoaffective Disorder; Schizophreniform Disorder
- Interventions
- Olanzapine or amisulpride
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2009-12
- Completion
- 2015-03
- Enrolment
- 350
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizoaffective Disorder; Schizophreniform DisorderInterventionOlanzapine or amisulpridePhaseNot applicableRegistry statusCompletedIdentification and Treatment Response Prediction of Antipsychotic-Related Metabolic Syndrome
NCT00956189 · start 2009-11
Registered record
- Registry ID
- NCT00956189
- Conditions
- Metabolic Syndrome X
- Interventions
- amisulpride; aripiprazole
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2009-11
- Completion
- 2012-10
- Enrolment
- 132
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMetabolic Syndrome XInterventionamisulpride; aripiprazolePhaseNot applicableRegistry statusCompletedPan European Collaboration on Antipsychotic Naive Schizophrenia (PECANS)
NCT01154829 · start 2008-12
Registered record
- Registry ID
- NCT01154829
- Conditions
- Schizophrenia
- Interventions
- amisulpride; aripiprazole
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-12
- Completion
- 2016-05
- Enrolment
- 136
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionamisulpride; aripiprazolePhaseNot applicableRegistry statusCompletedBenzamide Derivates as Treatment of Clozapine-induced Hypersalivation
NCT00534573 · start 2008-11
Registered record
- Registry ID
- NCT00534573
- Conditions
- Clozapine-induced Hypersalivation
- Interventions
- Amisulpride, Moclobemide
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2008-11
- Completion
- 2009-01
- Enrolment
- 54
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionClozapine-induced HypersalivationInterventionAmisulpride, MoclobemidePhasePhase 3Registry statusCompletedA Randomized, Double-blind, Comparison of the Efficacy and Safety of Amisulpride Versus Low-dose Amisulpride Plus Low-dose Sulpiride in the Treatment of Schizophrenia
NCT01615185 · start 2008-01
Registered record
- Registry ID
- NCT01615185
- Conditions
- Schizophrenia
- Interventions
- full-dose amisulpride
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2008-01
- Completion
- 2011-12
- Enrolment
- 96
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionfull-dose amisulpridePhasePhase 4Registry statusTerminatedCharacterize The Modulatory Effects Of Dopamine D2/D3 Receptor Agonist And Antagonist Drugs On Compulsive Behaviors
NCT00471588 · start 2006-08
Registered record
- Registry ID
- NCT00471588
- Conditions
- Obsessive-Compulsive Disorder
- Interventions
- Pramipexole, Amisulpride
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2006-08
- Completion
- 2007-12
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObsessive-Compulsive DisorderInterventionPramipexole, AmisulpridePhasePhase 1Registry statusCompletedAmisulpride in Schizophrenic Acute Phase Patients
NCT00436371 · start 2005-05
Registered record
- Registry ID
- NCT00436371
- Conditions
- Schizophrenia
- Interventions
- Amisulpride
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2005-05
- Completion
- Not recorded
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionAmisulpridePhasePhase 4Registry statusCompleted