Dextromethorphan Polistirex
FDA-approved product (suspension, extended release, oral), marketed as Delsym, Dextromethorphan Polistirex.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Allergic disease
- Common cold
- Cough
- Fever
- Headache
- Nasal congestion
- Sinusitis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Other nervous system drugs; Opium alkaloids and derivatives
- FDA pharmacologic class
- Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate 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 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- MRSA40.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli41.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae27.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis38.7% 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
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 Dextromethorphan Polistirex 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.
Bupropion Stereoselective Disposition and CYP2D6-mediated Drug Interactions in Healthy Volunteers
NCT03420469 · start 2018-06-05
Registered record
- Registry ID
- NCT03420469
- Conditions
- Adverse Effect of Drug Therapy Metabolism Medications (Diagnosis)
- Interventions
- Bupropion
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2018-06-05
- Completion
- 2019-05-01
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdverse Effect of Drug Therapy Metabolism Medications (Diagnosis)InterventionBupropionPhaseEarly phase 1Registry statusCompletedEffects of Repeated Doses of Lu AF35700 on Drug Metabolizing Enzymes
NCT03195946 · start 2017-06-16
Registered record
- Registry ID
- NCT03195946
- Conditions
- Drug Reactions
- Interventions
- Lu AF35700; Midazolam; Cocktail of CYP450 substrates
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-06-16
- Completion
- 2018-01-03
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDrug ReactionsInterventionLu AF35700; Midazolam; Cocktail of CYP450 substratesPhasePhase 1Registry statusCompletedDextromethorphan Use in Multimodal Analgesia Regimens for Total Knee Arthroplasty
NCT02987920 · start 2017-01
Registered record
- Registry ID
- NCT02987920
- Conditions
- Pain, Postoperative
- Interventions
- Dextromethorphan; Placebo - Concentrate; Acetaminophen; Oxycodone; Celecoxib; Pantoprazole; Ketorolac; Gabapentin; Hydromorphone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2017-01
- Completion
- 2018-01
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPain, PostoperativeInterventionDextromethorphan; Placebo - Concentrate; Acetaminophen; Oxycodone +5 morePhasePhase 4Registry statusTerminatedAn Open-label Drug-Drug Interaction Study to Evaluate the Effect of BCX7353 on Cytochrome P450 Enzyme Activity Using Probe Substrates
NCT02819102 · start 2016-03
Registered record
- Registry ID
- NCT02819102
- Conditions
- Hereditary Angioedema
- Interventions
- BCX7353 and probes
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2016-03
- Completion
- 2016-06
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHereditary AngioedemaInterventionBCX7353 and probesPhasePhase 1Registry statusCompletedEffectiveness, Safety, and Health-Related Outcomes of NUEDEXTA® in Nursing Home Patients With Pseudobulbar Affect (PBA)
NCT02496039 · start 2015-09
Registered record
- Registry ID
- NCT02496039
- Conditions
- Pseudobulbar Affect (Involuntary Laughing and/or Crying)
- Interventions
- NUEDEXTA®
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2015-09
- Completion
- 2016-05
- Enrolment
- 5
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPseudobulbar Affect (Involuntary Laughing and/or Crying)InterventionNUEDEXTA®PhasePhase 4Registry statusTerminatedCortical Metrics in Intervention Trials With Autism Spectrum Disorders
NCT02212275 · start 2015-08
Registered record
- Registry ID
- NCT02212275
- Conditions
- Autism Spectrum Disorders
- Interventions
- Dextromethophan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Withdrawn
- Start
- 2015-08
- Completion
- 2016-07
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutism Spectrum DisordersInterventionDextromethophanPhasePhase 2 / Phase 3Registry statusWithdrawnEfficacy, Safety and Tolerability of AVP-786 for the Treatment of Agitation in Patients With Dementia of the Alzheimer's Type
NCT02442765 · start 2015-07-23
Registered record
- Registry ID
- NCT02442765
- Conditions
- Agitation in Patients With Dementia of the Alzheimer's Type
- Interventions
- AVP-786; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2015-07-23
- Completion
- 2019-02-27
- Enrolment
- 387
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAgitation in Patients With Dementia of the Alzheimer's TypeInterventionAVP-786; PlaceboPhasePhase 3Registry statusCompletedPharmacokinetic Study to Evaluate the Effect of a Single Dose of Guselkumab (CNTO 1959) on CYP 450 Enzyme Activities After Subcutaneous Administration in Participants With Psoriasis
NCT02397382 · start 2015-06-18
Registered record
- Registry ID
- NCT02397382
- Conditions
- Psoriasis
- Interventions
- Guselkumab; Midazolam; Warfarin; Omeprazole; Dextromethorphan; Caffeine
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-06-18
- Completion
- 2016-08-31
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsoriasisInterventionGuselkumab; Midazolam; Warfarin; Omeprazole +2 morePhasePhase 1Registry statusCompletedAn Open Label, Single Dose, Three Part Study to Assess the Effects of Rolapitant (2 mg/mL IV Solution) on the Pharmacokinetics of Digoxin; Sulfasalazine; and the Cooperstown Cocktail (Midazolam, Omeprazole, Warfarin, Caffeine, and Dextromethorphan in Healthy Subjects
NCT02434861 · start 2015-05
Registered record
- Registry ID
- NCT02434861
- Conditions
- Chemotherapy-induced Nausea and Vomiting
- Interventions
- Rolapitant; Digoxin; Sulfasalazine; Cooperstown Cocktail
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-05
- Completion
- 2015-08
- Enrolment
- 102
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChemotherapy-induced Nausea and VomitingInterventionRolapitant; Digoxin; Sulfasalazine; Cooperstown CocktailPhasePhase 1Registry statusCompletedPilot Study Using an NMDA Antagonist to Modulate Transcranial Direct Current Stimulation (tDCS) Effects on Sensory Discrimination
NCT02426983 · start 2015-04
Registered record
- Registry ID
- NCT02426983
- Conditions
- Schizophrenia
- Interventions
- Direct Current Stimulation; Dextromethorphan
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Unknown
- Start
- 2015-04
- Completion
- 2016-04
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophreniaInterventionDirect Current Stimulation; DextromethorphanPhasePhase 1 / Phase 2Registry statusUnknownDrug Interaction Study Between AVP-923 and Itraconazole and Between AVP-786 and Itraconazole in Healthy Adult Subejcts
NCT02402595 · start 2015-03-01
Registered record
- Registry ID
- NCT02402595
- Conditions
- Healthy
- Interventions
- AVP-923; AVP-786; Itraconazole
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2015-03-01
- Completion
- 2015-07-01
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionAVP-923; AVP-786; ItraconazolePhasePhase 1Registry statusCompletedDextromethorphan in Chemotherapy-induced Peripheral Neuropathy Management
NCT02271893 · start 2014-11-25
Registered record
- Registry ID
- NCT02271893
- Conditions
- Chemotherapy-induced Peripheral Neuropathy
- Interventions
- Dextromethorphan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2014-11-25
- Completion
- 2022-04-21
- Enrolment
- 19
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChemotherapy-induced Peripheral NeuropathyInterventionDextromethorphanPhasePhase 2Registry statusTerminatedNuedexta for the Prevention and Modification of Disease Progression in Episodic Migraine
NCT02176018 · start 2014-08
Registered record
- Registry ID
- NCT02176018
- Conditions
- Episodic Migraine
- Interventions
- Dextromethorphan and quinidine; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2014-08
- Completion
- 2017-03
- Enrolment
- 76
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEpisodic MigraineInterventionDextromethorphan and quinidine; PlaceboPhasePhase 2Registry statusCompletedEfficacy, Safety, and Tolerability Study of AVP-786 as an Adjunctive Therapy in Patients With Major Depressive Disorder With an Inadequate Response to Antidepressant Treatment
NCT02153502 · start 2014-07-01
Registered record
- Registry ID
- NCT02153502
- Conditions
- Depressive Disorder, Treatment-Resistant
- Interventions
- AVP-786 (d6-dextromethorphan hydrobromide and quinidine sulfate combination); Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2014-07-01
- Completion
- 2016-02-01
- Enrolment
- 206
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDepressive Disorder, Treatment-ResistantInterventionAVP-786 (d6-dextromethorphan hydrobromide and quinidine sulfate combination); PlaceboPhasePhase 2Registry statusCompletedA Study to Investigate the Glucose Lowering Effects of Dextromethorphan Alone or in Combination With Sitagliptin in Subjects With Type 2 Diabetes Mellitus (T2DM) After an Oral Glucose Tolerance Test
NCT01936025 · start 2013-10
Registered record
- Registry ID
- NCT01936025
- Conditions
- Type 2 Diabetes Mellitus
- Interventions
- Dextromethorphan; Sitagliptin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2013-10
- Completion
- 2014-04
- Enrolment
- 34
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionType 2 Diabetes MellitusInterventionDextromethorphan; Sitagliptin; PlaceboPhasePhase 2Registry statusCompleted