Paliperidone
FDA-approved product (tablet, extended release, oral), marketed as Invega, Paliperidone.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Mental or behavioural disorder
- Psychosis
- Schizoaffective disorder
- Schizophrenia
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 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- MRSA67.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli46.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae43.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- M. tuberculosis59.5% 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
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 Paliperidone 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.
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm95.6% AI-predicted activityagainst MRSALab records exist50+ registered studies
- TaurursodiolExisting use: Bile acids and derivatives79.6% AI-predicted activityagainst MRSA43 registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome74.5% AI-predicted activityagainst MRSA50+ registered studies
- PlecanatideExisting use: Constipation74.4% AI-predicted activityagainst MRSA15 registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia74.2% AI-predicted activityagainst MRSA50+ registered studies
- PosaconazoleExisting use: Aspergillosis, Candidiasis, Coccidioidomycosis and 2 more72.2% AI-predicted activityagainst MRSA50+ registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma70.6% AI-predicted activityagainst MRSA50+ registered studies
- TemsirolimusExisting use: Cancer, Clear cell renal carcinoma, Mantle cell lymphoma and 2 more70.1% AI-predicted activityagainst MRSA50+ registered studies
- Quizartinib DihydrochlorideExisting use: Acute myeloid leukemia, Myeloid leukemia70.0% AI-predicted activityagainst MRSA4 registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more70.0% AI-predicted activityagainst MRSA50+ registered studies
- Deoxycholic AcidExisting use: Other dermatologicals69.3% AI-predicted activityagainst MRSA50+ registered studies
- ChenodiolExisting use: Cerebrotendinous xanthomatosis, Inborn errors of metabolism69.2% AI-predicted activityagainst MRSA30 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Bioequivalence Study of PP3M in Patients With Schizophrenia
NCT07493551 · start 2024-10-09
Registered record
- Registry ID
- NCT07493551
- Conditions
- Schizophrenia
- Interventions
- Paliperidone Palmitate Injection (3M)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2024-10-09
- Completion
- 2026-12-31
- Enrolment
- 260
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionPaliperidone Palmitate Injection (3M)PhaseNot applicableRegistry statusRecruitingMultidisciplinary Design to Optimize Schizophrenia Treatment Based on Multi-omics Data and Systems Biology Analysis
NCT06060886 · start 2023-11-01
Registered record
- Registry ID
- NCT06060886
- Conditions
- Schizophrenia; Treatment-resistant Schizophrenia; Side Effect; Lipid Metabolism Disorders; Diabetes; NAFLD; Psychosis
- Interventions
- Aripiprazole; Paliperidone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2023-11-01
- Completion
- 2025-12-31
- Enrolment
- 244
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Treatment-resistant Schizophrenia; Side Effect; Lipid Metabolism Disorders +3 moreInterventionAripiprazole; PaliperidonePhasePhase 4Registry statusUnknownRelative Bioavailability of LY03010 Compared to Listed Drug
NCT04922593 · start 2021-01-13
Registered record
- Registry ID
- NCT04922593
- Conditions
- Schizophrenia; Psychotic Disorders; Mood Disorders; Schizophrenia Spectrum; Mental Disorders; Antipsychotic Agents; Tranquilizing Agents; Central Nervous System Depressants; Physiological Effects of Drugs; Psychotropic Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action
- Interventions
- LY03010; paliperidone palmitate; INVEGA SUSTENNA
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2021-01-13
- Completion
- 2022-04-15
- Enrolment
- 281
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Psychotic Disorders; Mood Disorders; Schizophrenia Spectrum +8 moreInterventionLY03010; paliperidone palmitate; INVEGA SUSTENNAPhasePhase 1Registry statusCompletedEvaluate the PK of LY03010 Process 1 and Process 2 Drug Product vs INVEGA SUSTENNA After Intramuscular Injection in Schizophrenia Patients
NCT04572685 · start 2020-01-22
Registered record
- Registry ID
- NCT04572685
- Conditions
- Schizophrenia Patients
- Interventions
- Paliperidone Palmitate
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2020-01-22
- Completion
- 2020-08-20
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia PatientsInterventionPaliperidone PalmitatePhasePhase 1Registry statusCompletedA Study of Paliperidone Palmitate 6-Month Formulation
NCT04072575 · start 2019-09-19
Registered record
- Registry ID
- NCT04072575
- Conditions
- Schizophrenia
- Interventions
- PP6M injection Dose 1; PP6M injection Dose 2
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2019-09-19
- Completion
- 2022-05-03
- Enrolment
- 178
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionPP6M injection Dose 1; PP6M injection Dose 2PhasePhase 3Registry statusCompletedSubstance Misuse To Psychosis for Stimulants
NCT03485417 · start 2019-06-01
Registered record
- Registry ID
- NCT03485417
- Conditions
- Stimulant Use With Stimulant-Induced Psychotic Disorder (Diagnosis); Schizophrenia and Related Disorders; Stimulant Dependence; Stimulant Abuse; Pharmacotherapy
- Interventions
- Aripiprazole; Paliperidone; Treatment as Usual
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2019-06-01
- Completion
- 2025-05-31
- Enrolment
- 165
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionStimulant Use With Stimulant-Induced Psychotic Disorder (Diagnosis); Schizophrenia and Related Disorders; Stimulant Dependence; Stimulant Abuse +1 moreInterventionAripiprazole; Paliperidone; Treatment as UsualPhasePhase 2 / Phase 3Registry statusCompletedA Study to Evaluate the Ability of Conducting a Study of Oral Risperidone Followed by Paliperidone Palmitate in Rwandan Healthcare Facilities
NCT03713658 · start 2018-10-18
Registered record
- Registry ID
- NCT03713658
- Conditions
- Schizophrenia
- Interventions
- Risperidone 3 mg; Paliperidone Palmitate 50 mg eq.; Paliperidone Palmitate 75 mg eq.; Paliperidone Palmitate 100 mg eq.; Paliperidone Palmitate 150 mg eq.; Paliperidone Palmitate 175 mg eq.; Paliperidone Palmitate 263 mg eq.; Paliperidone Palmitate 350 mg eq.; Paliperidone Palmitate 525 mg eq.
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2018-10-18
- Completion
- 2019-12-02
- Enrolment
- 34
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionRisperidone 3 mg; Paliperidone Palmitate 50 mg eq.; Paliperidone Palmitate 75 mg eq.; Paliperidone Palmitate 100 mg eq. +5 morePhasePhase 4Registry statusCompletedA Study to Analyze the Impact of Treatment With Paliperidone Palmitate on Clinical Outcomes and Hospital Resource Utilization in Adult Participants With Schizophrenia in Portugal
NCT03666715 · start 2018-08-07
Registered record
- Registry ID
- NCT03666715
- Conditions
- Schizophrenia
- Interventions
- Oral Antipsychotics (OAPs); Paliperidone Palmitate 1-Month Formulation (PP1M)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2018-08-07
- Completion
- 2021-05-31
- Enrolment
- 55
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionOral Antipsychotics (OAPs); Paliperidone Palmitate 1-Month Formulation (PP1M)PhaseNot recordedRegistry statusCompletedA Study of Paliperidone Palmitate 6-Month Formulation
NCT03345342 · start 2017-11-20
Registered record
- Registry ID
- NCT03345342
- Conditions
- Schizophrenia
- Interventions
- PP6M; PP3M 350 mg eq.; PP3M 525 mg eq.; PP1M; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2017-11-20
- Completion
- 2020-05-08
- Enrolment
- 841
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionPP6M; PP3M 350 mg eq.; PP3M 525 mg eq.; PP1M +1 morePhasePhase 3Registry statusCompletedThe Effect of a Community-based LAI-treated Management Model on the Violence Risk of Patients With Schizophrenia
NCT03080194 · start 2017-04
Registered record
- Registry ID
- NCT03080194
- Conditions
- Schizophrenia
- Interventions
- paliperidone palmitate; control group
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2017-04
- Completion
- 2018-04
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionpaliperidone palmitate; control groupPhasePhase 4Registry statusUnknownAripiprazole, Abilify Maintena Collaborative Clinical Protocol
NCT02472652 · start 2015-06
Registered record
- Registry ID
- NCT02472652
- Conditions
- Sexual Dysfunction
- Interventions
- Abilify Maintena
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2015-06
- Completion
- 2017-03-01
- Enrolment
- 2
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSexual DysfunctionInterventionAbilify MaintenaPhasePhase 4Registry statusTerminatedEvaluation of the Necessity of Long-term Pharmacological Treatment With Antipsychotics in Schizophrenic Patients
NCT02307396 · start 2015-02-01
Registered record
- Registry ID
- NCT02307396
- Conditions
- Schizophrenia; Schizophrenia and Disorders With Psychotic Features; Schizoaffective Disorders
- Interventions
- Olanzapine; Amisulpride; Risperidone; Haloperidol; Quetiapine; Perphenazine; Sulpiride; bromperidol; Zuclopenthixol; Thioridazine; Paliperidone; Ziprasidone; Benperidol; Fluspirilene; Pimozide; Perazine; Fluphenazine; Flupentixole; Sertindole
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2015-02-01
- Completion
- 2016-06-22
- Enrolment
- 21
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizophrenia and Disorders With Psychotic Features; Schizoaffective DisordersInterventionOlanzapine; Amisulpride; Risperidone; Haloperidol +15 morePhasePhase 4Registry statusCompletedA Concierge Model of CAE Plus LAI in Individuals With Schizophrenia at Risk for Treatment Non-adherence and Homelessness
NCT02085447 · start 2014-05
Registered record
- Registry ID
- NCT02085447
- Conditions
- Psychotic Disorders; Schizophrenia; Schizoaffective Disorder; Medication Adherence; Medication Non-Adherence
- Interventions
- CAE-L
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2014-05
- Completion
- 2016-12
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsychotic Disorders; Schizophrenia; Schizoaffective Disorder; Medication Adherence +1 moreInterventionCAE-LPhaseNot applicableRegistry statusCompletedLong Acting Paliperidone in Dually Diagnosed People With Schizophrenia: An Open-label Pilot Study
NCT01584466 · start 2014-01
Registered record
- Registry ID
- NCT01584466
- Conditions
- Schizophrenia
- Interventions
- Paliperidone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Withdrawn
- Start
- 2014-01
- Completion
- 2014-01
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionPaliperidonePhaseNot applicableRegistry statusWithdrawnAn Observational Drug Utilization Study of Asenapine in the United Kingdom (P08308)
NCT01498770 · start 2013-04-01
Registered record
- Registry ID
- NCT01498770
- Conditions
- Bipolar Disorder
- Interventions
- Asenapine; Aripiprazole; Quetiapine; Risperidone; Olanzapine; Ziprasidone; Iloperidone; Paliperidone; Lurasidone; Clozapine; Amisulpride; Sertindole; Zotepine
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2013-04-01
- Completion
- 2017-12-21
- Enrolment
- 42
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBipolar DisorderInterventionAsenapine; Aripiprazole; Quetiapine; Risperidone +9 morePhaseNot recordedRegistry statusCompleted