Aripiprazole
FDA-approved product (tablet, oral), marketed as Abilify, Abilify Asimtufii, Abilify Maintena Kit and 4 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Aggressive behavior
- Agitation
- Autism
- Bipolar disorder
- Bipolar I disorder
- Depressive disorder
- Major depressive disorder
- Psychosis
- Schizoaffective disorder
- Schizophrenia
- Tourette syndrome
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other antipsychotics
- FDA pharmacologic class
- Atypical Antipsychotic 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- MRSA48.3% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli48.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae38.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis51.4% 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 Aripiprazole 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.
A Trial to Explore Acceptance and Performance of Using a Digital Medicine System With Healthcare Professionals and Adults With Schizophrenia, Schizoaffective Disorder, or First Episode Psychosis on an Oral Atypical Antipsychotic
NCT03568500 · start 2018-05-21
Registered record
- Registry ID
- NCT03568500
- Conditions
- Schizophrenia; Schizoaffective Disorder; First Episode Psychosis
- Interventions
- Digital Medicine System; Aripiprazole; Olanzapine; Quetiapine; Risperidone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2018-05-21
- Completion
- 2019-09-06
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizoaffective Disorder; First Episode PsychosisInterventionDigital Medicine System; Aripiprazole; Olanzapine; Quetiapine +1 morePhasePhase 4Registry statusCompletedCAE Plus LAI in Individuals With Bipolar Disorder at Risk for Treatment Non-adherence (BD-CAEL)
NCT03408873 · start 2018-04-01
Registered record
- Registry ID
- NCT03408873
- Conditions
- Bipolar Disorder; Medication Adherence; Medication Non Adherence
- Interventions
- Abilify Maintena; Customized Adherence Enhancement (CAE)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2018-04-01
- Completion
- 2020-05-06
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBipolar Disorder; Medication Adherence; Medication Non AdherenceInterventionAbilify Maintena; Customized Adherence Enhancement (CAE)PhasePhase 4Registry statusCompletedTrajectories of Treatment Response as Window Into the Heterogeneity of Psychosis: a Longitudinal Multimodal Imaging Study
NCT03442101 · start 2018-04-01
Registered record
- Registry ID
- NCT03442101
- Conditions
- Psychosis
- Interventions
- Patients with psychosis will be treated with known antipsychotic medication
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2018-04-01
- Completion
- 2026-12-31
- Enrolment
- 156
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsychosisInterventionPatients with psychosis will be treated with known antipsychotic medicationPhaseNot recordedRegistry statusActive not recruitingPharmacologic Treatment of Acute Episode of Schizophrenia: a Real World Study
NCT03289026 · start 2017-09-01
Registered record
- Registry ID
- NCT03289026
- Conditions
- Acute Schizophrenia Episode
- Interventions
- Aripiprazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2017-09-01
- Completion
- 2021-02-02
- Enrolment
- 770
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Schizophrenia EpisodeInterventionAripiprazolePhasePhase 4Registry statusCompletedTrial to Evaluate the Short-term Safety & Efficacy of Brexpiprazole Monotherapy in the Treatment of Adolescents With Schizophrenia
NCT03198078 · start 2017-06-30
Registered record
- Registry ID
- NCT03198078
- Conditions
- Schizophrenia
- Interventions
- Brexpiprazole (OPC-34712); Aripiprazole; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2017-06-30
- Completion
- 2023-04-03
- Enrolment
- 316
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionBrexpiprazole (OPC-34712); Aripiprazole; PlaceboPhasePhase 3Registry statusCompletedExploratory Trial to Assess the Functionality of an Integrated Call Center for the Digital Medicine System
NCT02722967 · start 2016-03
Registered record
- Registry ID
- NCT02722967
- Conditions
- Schizophrenia; Major Depressive Disorder; Bipolar I Disorder
- Interventions
- Aripiprazole + IEM (Ingestible Event Marker)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2016-03
- Completion
- 2016-09
- Enrolment
- 49
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Major Depressive Disorder; Bipolar I DisorderInterventionAripiprazole + IEM (Ingestible Event Marker)PhasePhase 2Registry statusCompletedEfficacy of Memantine add-on in the Treatment of Bipolar Disorder (Type I) Nonresponders or Partial Responders Patients
NCT02630888 · start 2014-08
Registered record
- Registry ID
- NCT02630888
- Conditions
- Bipolar Disorder
- Interventions
- Memantine; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2014-08
- Completion
- 2020-09
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBipolar DisorderInterventionMemantine; PlaceboPhasePhase 2Registry statusUnknownSubstudy of the Accuracy of Ingestible Event Marker (IEM) Detection by the Medical Information Device #1 (MIND1)
NCT02091882 · start 2014-03-21
Registered record
- Registry ID
- NCT02091882
- Conditions
- Device Latency
- Interventions
- Placebo; Combination product of Aripiprazole + IEM + Sensor + MIND1 Application
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-03-21
- Completion
- 2014-04-18
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDevice LatencyInterventionPlacebo; Combination product of Aripiprazole + IEM + Sensor + MIND1 ApplicationPhasePhase 4Registry statusCompletedAssess the Efficacy and Safety of ASC-01 in Patients With Major Depressive Disorder
NCT02046564 · start 2014-02
Registered record
- Registry ID
- NCT02046564
- Conditions
- Major Depressive Disorder
- Interventions
- ASC-01; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2014-02
- Completion
- 2016-09
- Enrolment
- 412
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMajor Depressive DisorderInterventionASC-01; PlaceboPhasePhase 3Registry statusCompletedBrexpiprazole (OPC-34712) Trial in the Treatment of Adults With Acute Schizophrenia
NCT02054702 · start 2014-02
Registered record
- Registry ID
- NCT02054702
- Conditions
- Schizophrenia
- Interventions
- Brexpiprazole; Aripiprazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2014-02
- Completion
- 2014-07
- Enrolment
- 97
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionBrexpiprazole; AripiprazolePhasePhase 3Registry statusCompleted1/2-MC4R Genotype and Pediatric Antipsychotic Drug- Induced Weight Gain
NCT01844700 · start 2013-07
Registered record
- Registry ID
- NCT01844700
- Conditions
- High Risk MC4R Genotype; Low Risk MC4R Genotype; One Week or Less Antipsychotic Lifetime Exposure
- Interventions
- Ziprasidone; aripiprazole, quetiapine, or risperidone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2013-07
- Completion
- 2014-04
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHigh Risk MC4R Genotype; Low Risk MC4R Genotype; One Week or Less Antipsychotic Lifetime ExposureInterventionZiprasidone; aripiprazole, quetiapine, or risperidonePhasePhase 4Registry statusTerminatedAripiprazole (Abilify®) as an Adjunctive Treatment for Inadequate Response in Major Depressive Disorder
NCT01696617 · start 2012-02-10
Registered record
- Registry ID
- NCT01696617
- Conditions
- Major Depressive Disorder
- Interventions
- Aripiprazole 6-week group; Aripiprazole 8-week group
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2012-02-10
- Completion
- 2019-02
- Enrolment
- 46
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMajor Depressive DisorderInterventionAripiprazole 6-week group; Aripiprazole 8-week groupPhasePhase 4Registry statusCompletedLow-Dose Adjunctive Aripiprazole in the Treatment of Bipolar Depression: Double-Blind Placebo-Controlled Pilot Study
NCT01520350 · start 2012-02
Registered record
- Registry ID
- NCT01520350
- Conditions
- Bipolar Disorder; Depressive Episode
- Interventions
- Low dose Adjunctive Aripiprazole; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2012-02
- Completion
- 2013-06
- Enrolment
- 2
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBipolar Disorder; Depressive EpisodeInterventionLow dose Adjunctive Aripiprazole; placeboPhasePhase 3Registry statusTerminatedOpen-label Study to Compare Hospitalization Rates of Schizophrenic Patients Treated With Oral Antipsychotics Versus IM Depot Aripiprazole
NCT01509053 · start 2012-01
Registered record
- Registry ID
- NCT01509053
- Conditions
- Schizophrenia
- Interventions
- Aripiprazole (Abilify®) IM Depot Injection; Oral aripiprazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2012-01
- Completion
- 2012-10
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionAripiprazole (Abilify®) IM Depot Injection; Oral aripiprazolePhasePhase 3Registry statusTerminatedEfficacy & Safety Study of Once-weekly Oral Aripiprazole in Children and Adolescents With Tourette's Disorder (TD)
NCT01418352 · start 2011-08-02
Registered record
- Registry ID
- NCT01418352
- Conditions
- Tourette's Disorder
- Interventions
- Aripiprazole; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2011-08-02
- Completion
- 2014-03-12
- Enrolment
- 83
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionTourette's DisorderInterventionAripiprazole; PlaceboPhasePhase 3Registry statusCompleted