Nabilone
FDA-approved product (capsule, oral), marketed as Cesamet.
- Registered studies
- 35
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cancer
- Nausea
- Nausea and vomiting
- Post operative nausea and vomiting
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other antiemetics
- FDA pharmacologic class
- Cannabinoid 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. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA50.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli29.9% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae31.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis37.9% AI-predicted activityBelow 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
35registered 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 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 Nabilone 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.
- PlecanatideExisting use: Constipation52.2% AI-predicted activityagainst K. pneumoniae15 registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma51.3% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome50.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Terlipressin AcetateExisting use: Hepatorenal syndrome, Kidney failure, Renal insufficiency49.5% AI-predicted activityagainst K. pneumoniae7 registered studies
- LetermovirExisting use: Cytomegalovirus infection, Infection, Viral disease49.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Codeine SulfateExisting use: Cough, Drug dependence, Migraine disorder and 2 more48.8% AI-predicted activityagainst K. pneumoniae23 registered studies
- Bromocriptine MesylateExisting use: Acromegaly, Adenoma, Hyperprolactinemia and 4 more48.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- PimecrolimusExisting use: Atopic eczema, Eczematoid dermatitis48.3% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LypressinExisting use: Vasopressin and analogues48.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Degarelix AcetateExisting use: Prostate adenocarcinoma, Prostate cancer, Prostate carcinoma48.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more48.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Dolutegravir SodiumExisting use: HIV infection, HIV-1 infection47.9% AI-predicted activityagainst K. pneumoniae50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Efficacy of PP-01 in Mitigating Cannabis Withdrawal Symptoms in Adults With Cannabis Use Disorder
NCT07644052 · start 2026-06-17
Registered record
- Registry ID
- NCT07644052
- Conditions
- Cannabis Withdrawal
- Interventions
- PP-01; Nabilone; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2026-06-17
- Completion
- 2027-09
- Enrolment
- 420
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCannabis WithdrawalInterventionPP-01; Nabilone; PlaceboPhasePhase 3Registry statusRecruitingNabilone Use For Acute Pain in Inflammatory Bowel Disease Patients
NCT03422861 · start 2023-12
Registered record
- Registry ID
- NCT03422861
- Conditions
- Inflammatory Bowel Diseases
- Interventions
- Nabilone; Placebos
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2023-12
- Completion
- 2024-12
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInflammatory Bowel DiseasesInterventionNabilone; PlacebosPhaseNot applicableRegistry statusUnknownInvestigating the Effects of Nabilone on Endocannabinoid Metabolism
NCT05885685 · start 2023-10-31
Registered record
- Registry ID
- NCT05885685
- Conditions
- Healthy
- Interventions
- Nabilone Oral Capsule
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2023-10-31
- Completion
- 2025-12-05
- Enrolment
- 10
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionNabilone Oral CapsulePhasePhase 4Registry statusCompletedNabilone for Agitation in Frontotemporal Dementia
NCT05742698 · start 2023-03-07
Registered record
- Registry ID
- NCT05742698
- Conditions
- Frontotemporal Dementia; Frontotemporal Dementia, Behavioral Variant; Primary Progressive Aphasia; bvFTD; PPA; FTD
- Interventions
- Nabilone; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2023-03-07
- Completion
- 2025-12-31
- Enrolment
- 3
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFrontotemporal Dementia; Frontotemporal Dementia, Behavioral Variant; Primary Progressive Aphasia; bvFTD +2 moreInterventionNabilone; PlaceboPhasePhase 2Registry statusTerminatedCannabinoids and an Anti-inflammatory Diet for the Treatment of Neuropathic Pain After Spinal Cord Injury
NCT04057456 · start 2023-03-01
Registered record
- Registry ID
- NCT04057456
- Conditions
- Spinal Cord Injuries; Neuropathic Pain
- Interventions
- Placebo diet; Anti-inflammatory diet; Nabilone Capsules; Placebo capsules
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-03-01
- Completion
- 2024-12-01
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSpinal Cord Injuries; Neuropathic PainInterventionPlacebo diet; Anti-inflammatory diet; Nabilone Capsules; Placebo capsulesPhasePhase 3Registry statusCompletedEffect of PP-01 on Cannabis Withdrawal Syndrome
NCT05494437 · start 2022-10-27
Registered record
- Registry ID
- NCT05494437
- Conditions
- Cannabis Withdrawal
- Interventions
- PP-01 High Dose; PP-01 Low Dose; Placebo; Nabilone; Gabapentin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2022-10-27
- Completion
- 2023-08-21
- Enrolment
- 234
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCannabis WithdrawalInterventionPP-01 High Dose; PP-01 Low Dose; Placebo; Nabilone +1 morePhasePhase 2Registry statusCompletedDIalysis Symptom COntrol-Pruritus Outcome Trial
NCT05180968 · start 2022-08-02
Registered record
- Registry ID
- NCT05180968
- Conditions
- End Stage Renal Disease; Pruritus
- Interventions
- Nabilone 0.5 MG Oral Capsule; Placebo Nabilone
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-08-02
- Completion
- 2023-08-11
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEnd Stage Renal Disease; PruritusInterventionNabilone 0.5 MG Oral Capsule; Placebo NabilonePhasePhase 3Registry statusCompletedClinical Trial of Nabilone for Aggression in Adults With Intellectual and Developmental Disabilities
NCT05273320 · start 2022-03-17
Registered record
- Registry ID
- NCT05273320
- Conditions
- Intellectual Disability; Developmental Disability; Aggression; Behavior Problem
- Interventions
- Nabilone
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2022-03-17
- Completion
- 2025-08-14
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIntellectual Disability; Developmental Disability; Aggression; Behavior ProblemInterventionNabilonePhasePhase 1Registry statusCompletedMultimodal Assessment of Cannabinoid Target Engagement in Adults With Obsessive-Compulsive Disorder
NCT04880278 · start 2022-03-01
Registered record
- Registry ID
- NCT04880278
- Conditions
- Obsessive-Compulsive Disorder
- Interventions
- Nabilone; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Withdrawn
- Start
- 2022-03-01
- Completion
- 2024-05-08
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObsessive-Compulsive DisorderInterventionNabilone; PlaceboPhasePhase 1 / Phase 2Registry statusWithdrawnA Pilot Trial of Nabilone for the Treatment of Obesity
NCT04801641 · start 2021-09-17
Registered record
- Registry ID
- NCT04801641
- Conditions
- Obesity
- Interventions
- Placebo; Nabilone
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2021-09-17
- Completion
- 2023-08-14
- Enrolment
- 18
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObesityInterventionPlacebo; NabilonePhasePhase 2Registry statusTerminatedAdjunctive CB1 Agonist Nabilone in Inpatients With Active Suicidal Ideation
NCT04807829 · start 2021-04
Registered record
- Registry ID
- NCT04807829
- Conditions
- Suicidal Ideation
- Interventions
- Nabilone; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Withdrawn
- Start
- 2021-04
- Completion
- 2022-04
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSuicidal IdeationInterventionNabilone; PlaceboPhasePhase 2Registry statusWithdrawnNabilone for Agitation Blinded Intervention Trial
NCT04516057 · start 2021-02-01
Registered record
- Registry ID
- NCT04516057
- Conditions
- Alzheimer Disease; Agitation
- Interventions
- Nabilone; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2021-02-01
- Completion
- 2027-04
- Enrolment
- 112
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAlzheimer Disease; AgitationInterventionNabilone; PlaceboPhasePhase 3Registry statusRecruitingNabilone for Non-motor Symptoms in Parkinson's Disease
NCT03773796 · start 2018-08-06
Registered record
- Registry ID
- NCT03773796
- Conditions
- Parkinson Disease
- Interventions
- Nabilone 0.25 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2018-08-06
- Completion
- 2020-01-31
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParkinson DiseaseInterventionNabilone 0.25 mgPhasePhase 3Registry statusCompletedNabilone for Non-motor Symptoms in Parkinson's Disease
NCT03769896 · start 2017-10-03
Registered record
- Registry ID
- NCT03769896
- Conditions
- Parkinson Disease
- Interventions
- Nabilone 0.25 mg; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2017-10-03
- Completion
- 2019-07-15
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionParkinson DiseaseInterventionNabilone 0.25 mg; PlaceboPhasePhase 2Registry statusCompletedCannabinoid Medication for Adults With OCD
NCT02911324 · start 2016-09
Registered record
- Registry ID
- NCT02911324
- Conditions
- Obsessive-Compulsive Disorder
- Interventions
- Nabilone; Exposure and Response Prevention Therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2016-09
- Completion
- 2019-01
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionObsessive-Compulsive DisorderInterventionNabilone; Exposure and Response Prevention TherapyPhasePhase 1 / Phase 2Registry statusCompleted