Cetirizine Hydrochloride
FDA-approved product (tablet, oral), marketed as Cetirizine Hydrochloride, Cetirizine Hydrochloride Allergy, Cetirizine Hydrochloride Hives and 11 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Allergic conjunctivitis
- Allergic disease
- Allergic rhinitis
- Eye allergy
- Nasal congestion
- Pruritus
- Rhinitis, Allergic, Perennial
- Seasonal allergic rhinitis
- Urticaria
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Piperazine derivatives; Other antiallergics
- 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- MRSA43.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli40.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae26.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis54.8% 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 Cetirizine Hydrochloride 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.
EFFECT OF AYURVEDA TREATMENT IN ALLERGIC RHINITIS
NCT07626099 · start 2028-06-30
Registered record
- Registry ID
- NCT07626099
- Conditions
- Allergic Rhinitis (AR)
- Interventions
- AYURVEDA treatment protocol; Control(Citrizine 10mg)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2028-06-30
- Completion
- 2030-12-30
- Enrolment
- 104
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic Rhinitis (AR)InterventionAYURVEDA treatment protocol; Control(Citrizine 10mg)PhaseNot applicableRegistry statusNot yet recruitingIMPOWER-QoL: IMPact Of Discontinuing Premedication for WEekly Paclitaxel on bReast Cancer Patient's Quality Of Life
NCT07478315 · start 2026-03-15
Registered record
- Registry ID
- NCT07478315
- Conditions
- Breast Cancer
- Interventions
- withdrawal of the premedication
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Not yet recruiting
- Start
- 2026-03-15
- Completion
- 2026-12-31
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBreast CancerInterventionwithdrawal of the premedicationPhaseNot applicableRegistry statusNot yet recruitingRelative 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 statusRecruitingEvaluation of the Omission of Dexamethasone in Premedication Regimens During Paclitaxel Treatment
NCT06118710 · start 2024-06-25
Registered record
- Registry ID
- NCT06118710
- Conditions
- Cancer
- Interventions
- Dexamethasone; H1 Antihistaminics
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2024-06-25
- Completion
- 2027-08-01
- Enrolment
- 500
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCancerInterventionDexamethasone; H1 AntihistaminicsPhasePhase 4Registry statusRecruitingTopical Cetirizine in Treatment of Localized Alopecia Areata
NCT05803070 · start 2023-09-01
Registered record
- Registry ID
- NCT05803070
- Conditions
- Alopecia Areata
- Interventions
- Topical Cetirizine 1 %; Topical betamethasone valerate 0.1%
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2023-09-01
- Completion
- 2024-10-01
- Enrolment
- 59
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAlopecia AreataInterventionTopical Cetirizine 1 %; Topical betamethasone valerate 0.1%PhaseNot recordedRegistry 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 statusCompletedEfficacy of TCM Capsules Lian Hua Qing Wen Jiao Nang in Mild COVID-19 Patients
NCT05275933 · start 2022-04-05
Registered record
- Registry ID
- NCT05275933
- Conditions
- COVID-19
- Interventions
- TCM intervention; Placebo intervention
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2022-04-05
- Completion
- 2023-11-22
- Enrolment
- 93
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID-19InterventionTCM intervention; Placebo interventionPhasePhase 2 / Phase 3Registry statusCompletedThe 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 statusTerminatedC Reactive Protein in Home Quarantined Coronavirus Disease 2019 (COVID -19) Patients.
NCT04935515 · start 2021-04-15
Registered record
- Registry ID
- NCT04935515
- Conditions
- COVID -19
- Interventions
- Oral Antibiotic, Antihistamine, Anti-inflammatory, Multivitamins; Oral low dose steroid; Intravenous Antibiotics with Low dose steroid.; Oral anti-coagulant
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2021-04-15
- Completion
- 2021-06-06
- Enrolment
- 25
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCOVID -19InterventionOral Antibiotic, Antihistamine, Anti-inflammatory, Multivitamins; Oral low dose steroid; Intravenous Antibiotics with Low dose steroid.; Oral anti-coagulantPhaseNot applicableRegistry statusCompletedEfficacy 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 statusCompletedEfficacy of Oral Supplementation of Probiotics in Children With Atopic Dermatitis
NCT04706559 · start 2021-01-03
Registered record
- Registry ID
- NCT04706559
- Conditions
- Atopic Dermatitis
- Interventions
- Probiotic sachet containing mixture of four strains i.e.Lactobacillus rhamnosus, Lactobacillus acidophilus, Bifidobacterium longum, and Saccharomyces boulardii; Conventional treatment
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2021-01-03
- Completion
- 2021-12-15
- Enrolment
- 98
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAtopic DermatitisInterventionProbiotic sachet containing mixture of four strains i.e.Lactobacillus rhamnosus, Lactobacillus acidophilus, Bifidobacterium longum, and Saccharomyces boulardii; Conventional treatmentPhaseNot applicableRegistry statusCompletedExploration of the Optimal Dosage of Cetirizine in the Treatment of Allergic Diseases in Chinese Children
NCT06288334 · start 2020-08-06
Registered record
- Registry ID
- NCT06288334
- Conditions
- Allergic Disease; Children
- Interventions
- 1-3 Cetirizine Pharmacokinetic samples
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2020-08-06
- Completion
- 2024-05-31
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic Disease; ChildrenIntervention1-3 Cetirizine Pharmacokinetic samplesPhasePhase 4Registry statusUnknownTopical 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 statusCompleted