Hydroxyzine Pamoate
FDA-approved product (capsule, oral), marketed as Atarax, Hydroxyzine, Hydroxyzine Hydrochloride 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
- Anxiety
- Anxiety disorder
- Neurotic disorder
- Pruritus
- Skin disease
- Urticaria
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Diphenylmethane derivatives
- 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- MRSA40.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli41.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae23.2% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis53.0% 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 Hydroxyzine Pamoate 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.
Relative Bioavailability Study to Evaluate Cetirizine HCl Gummy 10 mg and Cetirizine HCl Oral Tablets 10 mg
NCT04071821 · start 2025-05-01
Registered record
- Registry ID
- NCT04071821
- Conditions
- Allergy
- Interventions
- cetirizine HCl Gummy; Zyrtec tablet 10mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2025-05-01
- Completion
- 2025-09-30
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergyInterventioncetirizine HCl Gummy; Zyrtec tablet 10mgPhasePhase 1Registry statusUnknownThe Impact of Airway Allergic Diseases on Children's and Parents' Quality of Life
NCT06535087 · start 2024-07-20
Registered record
- Registry ID
- NCT06535087
- Conditions
- Pediatric Asthma; Rhinitis, Allergic; Quality of Life
- Interventions
- Subcutaneous immunotherapy / Standard Treatment for Asthma and Rhinitis
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Recruiting
- Start
- 2024-07-20
- Completion
- 2027-05-31
- Enrolment
- 600
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPediatric Asthma; Rhinitis, Allergic; Quality of LifeInterventionSubcutaneous immunotherapy / Standard Treatment for Asthma and RhinitisPhaseNot recordedRegistry statusRecruitingEfficacy of Hydroxyzine for Patients With Panic Disorder
NCT05737511 · start 2023-12-30
Registered record
- Registry ID
- NCT05737511
- Conditions
- Panic Disorder
- Interventions
- Hydroxyzine; Escitalopram Oxalate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2023-12-30
- Completion
- 2026-12-30
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPanic DisorderInterventionHydroxyzine; Escitalopram OxalatePhasePhase 4Registry statusNot yet recruitingRELIEF OF PSYCHOEMOTIONAL STRESS USING XENON SEDATION
NCT06080100 · start 2023-11-01
Registered record
- Registry ID
- NCT06080100
- Conditions
- Psychological Stress; Anesthesia; Anxiety; Xenon
- Interventions
- Xenon; premedication hydroxyzine 25 mg
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2023-11-01
- Completion
- 2026-09-01
- Enrolment
- 140
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPsychological Stress; Anesthesia; Anxiety; XenonInterventionXenon; premedication hydroxyzine 25 mgPhaseEarly phase 1Registry statusCompletedComparison Between Oral Melatonin and Hydroxyzine in Pediatric Patients Undergoing Adenotonsillectomy
NCT05680584 · start 2023-02-01
Registered record
- Registry ID
- NCT05680584
- Conditions
- Effect of Drug; Anxiety
- Interventions
- Melatonin 3 MG; Hydroxyzine Pill; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2023-02-01
- Completion
- 2024-01-30
- Enrolment
- 78
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEffect of Drug; AnxietyInterventionMelatonin 3 MG; Hydroxyzine Pill; PlaceboPhasePhase 1Registry statusUnknownThe Effect of Switching the H1-antagonist Clemastine to Cetirizine in Premedication Regimens During Paclitaxel Treatment
NCT06039137 · start 2022-06-01
Registered record
- Registry ID
- NCT06039137
- Conditions
- Solid Tumor
- Interventions
- Cetirizine; Clemastine IV
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2022-06-01
- Completion
- 2023-10-31
- Enrolment
- 395
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSolid TumorInterventionCetirizine; Clemastine IVPhaseNot recordedRegistry statusCompletedCLOZAPINE Response in Biotype-1
NCT04580134 · start 2022-03-01
Registered record
- Registry ID
- NCT04580134
- Conditions
- Schizophrenia; Schizoaffective Disorder; Bipolar 1 Disorder
- Interventions
- clozapine; risperidone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2022-03-01
- Completion
- 2027-04-30
- Enrolment
- 524
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSchizophrenia; Schizoaffective Disorder; Bipolar 1 DisorderInterventionclozapine; risperidonePhasePhase 4Registry statusRecruitingMelatonin Versus Hydroxizin for Pre Operative Anxiety in Elderly Patients With Hip Fracture
NCT05224167 · start 2022-03-01
Registered record
- Registry ID
- NCT05224167
- Conditions
- Preoperative Anxiety
- Interventions
- Melatonin 5 MG Sublingual Tablet; Hydroxyzine
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2022-03-01
- Completion
- 2022-07-30
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPreoperative AnxietyInterventionMelatonin 5 MG Sublingual Tablet; HydroxyzinePhaseNot applicableRegistry statusUnknownThe Effect of Cetirizine HCl on Exercise-induced Arterial Hypoxemia in Highly-trained Swimmers
NCT05095311 · start 2021-05-19
Registered record
- Registry ID
- NCT05095311
- Conditions
- Exercise-induced Arterial Hypoxemia
- Interventions
- Cetirizine HCl; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2021-05-19
- Completion
- 2022-04-27
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionExercise-induced Arterial HypoxemiaInterventionCetirizine HCl; PlaceboPhasePhase 4Registry statusTerminatedEfficacy of Antihistamine Drugs as Medical Expulsive Therapy Alone or in Combination With Alpha Blockers: A Prospective Randomized Controlled Study
NCT06754410 · start 2021-03-01
Registered record
- Registry ID
- NCT06754410
- Conditions
- Lower Ureteric Stones
- Interventions
- Tamsulosin; Cetirizine; Cetirizine + Tamsulosin; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2021-03-01
- Completion
- 2024-03-01
- Enrolment
- 480
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionLower Ureteric StonesInterventionTamsulosin; Cetirizine; Cetirizine + Tamsulosin; PlaceboPhasePhase 3Registry statusCompletedVirtual Reality Technology on Pain Perception and Anxiety Levels in Adolescents and Young Adults During Third Molar Germ Avulsion Surgery (VIDAMO)
NCT04609956 · start 2021-02-16
Registered record
- Registry ID
- NCT04609956
- Conditions
- Anxiety, Dental
- Interventions
- Virtual reality; Standard
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2021-02-16
- Completion
- 2024-05-28
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAnxiety, DentalInterventionVirtual reality; StandardPhaseNot applicableRegistry statusCompletedTopical Cetirizine 1% vs Minoxidil 5% Gel in Treatment of Androgenetic Alopecia
NCT04293822 · start 2020-06
Registered record
- Registry ID
- NCT04293822
- Conditions
- Androgenetic Alopecia
- Interventions
- Cetirizine; Minoxidil
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2020-06
- Completion
- 2021-11
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAndrogenetic AlopeciaInterventionCetirizine; MinoxidilPhasePhase 4Registry statusUnknownCetirizine Chewable Bioequivalence and Food Effect Study
NCT03772158 · start 2018-12-11
Registered record
- Registry ID
- NCT03772158
- Conditions
- Allergy
- Interventions
- Cetirizine 10mg; Cetirizine 10 mg; Cetirizine 10 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2018-12-11
- Completion
- 2019-02-03
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergyInterventionCetirizine 10mg; Cetirizine 10 mg; Cetirizine 10 mgPhasePhase 1Registry statusCompletedPresurgery Anxiolysis in Children Treated With Hydroxyzine Versus Non-pharmacological Intervention (Distractoria Technique Clown)
NCT03324828 · start 2017-11-01
Registered record
- Registry ID
- NCT03324828
- Conditions
- Anxiety
- Interventions
- Hydroxyzine; Clowns intervention
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2017-11-01
- Completion
- 2020-05-29
- Enrolment
- 170
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAnxietyInterventionHydroxyzine; Clowns interventionPhasePhase 4Registry statusTerminatedMast Cells in Male Pelvic Pain and and Lower Urinary Tract Dysfunction
NCT03167216 · start 2017-08-01
Registered record
- Registry ID
- NCT03167216
- Conditions
- Chronic Prostatitis With Chronic Pelvic Pain Syndrome
- Interventions
- Cromolyn Sodium; Cetirizine Hydrochloride
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Completed
- Start
- 2017-08-01
- Completion
- 2022-06-30
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Prostatitis With Chronic Pelvic Pain SyndromeInterventionCromolyn Sodium; Cetirizine HydrochloridePhaseEarly phase 1Registry statusCompleted