Azelastine Hydrochloride
FDA-approved product (spray, metered, nasal), marketed as Astelin, Astepro, Astepro Allergy and 5 more.
- Registered studies
- 48
- 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
- Rhinitis, Allergic, Perennial
- Seasonal allergic rhinitis
- Vasomotor rhinitis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Antiallergic agents, excl. corticosteroids; Other antihistamines for systemic use; 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 MRSA, E. coli 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- MRSA57.2% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli42.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae22.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis59.8% 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
48registered 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 Azelastine 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.
- UrsodiolExisting use: Biliary liver cirrhosis, Primary biliary cirrhosis69.2% AI-predicted activityagainst MRSA50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more69.2% AI-predicted activityagainst MRSA50+ registered studies
- Ganirelix AcetateExisting use: Female infertility, Positive regulation of ovulation, Reproductive Techniques, Assisted69.1% AI-predicted activityagainst MRSA50+ registered studies
- DanicopanExisting use: Acquired paroxysmal nocturnal hemoglobinuria, Hemoglobinuria, Paroxysmal, Hemolysis68.7% AI-predicted activityagainst MRSA30 registered studies
- Simeprevir SodiumExisting use: Chronic hepatitis C virus infection68.6% AI-predicted activityagainst MRSANo documented evidence found
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome68.3% AI-predicted activityagainst MRSA50+ registered studies
- Cholic AcidExisting use: Abnormality of the gastrointestinal tract, Inborn errors of metabolism, Liver disease and 1 more68.0% AI-predicted activityagainst MRSA50+ registered studies
- EptifibatideExisting use: Acute coronary syndrome, Acute myocardial infarction, Intermediate coronary syndrome and 2 more67.8% AI-predicted activityagainst MRSA35 registered studies
- AbarelixExisting use: Neoplasm67.7% AI-predicted activityagainst MRSA5 registered studies
- EverolimusExisting use: Adenoma sebaceum, Anaplastic astrocytoma, Angiomyolipoma and 18 more67.5% AI-predicted activityagainst MRSA50+ registered studies
- Paliperidone PalmitateExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.3% AI-predicted activityagainst MRSA50+ registered studies
- PaliperidoneExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Thermosensitive Gel Nasal Spray With Stem Cell Exosomes, Mupirocin, and DNase I for Chronic Sinusitis
NCT07635433 · start 2026-07-01
Registered record
- Registry ID
- NCT07635433
- Conditions
- Chronic Rhinosinusitis With Nasal Polyps
- Interventions
- Exosomes (hUC-MSC-Exo); Mupirocin; DNase I; Placebo Gel Matrix
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Not yet recruiting
- Start
- 2026-07-01
- Completion
- 2027-06-30
- Enrolment
- 108
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Rhinosinusitis With Nasal PolypsInterventionExosomes (hUC-MSC-Exo); Mupirocin; DNase I; Placebo Gel MatrixPhaseEarly phase 1Registry statusNot yet recruitingThermosensitive Gel Nasal Spray With Exosomes, Azelastine, and Interferon for Acute Phase of Chronic Sinusitis
NCT07635459 · start 2026-07-01
Registered record
- Registry ID
- NCT07635459
- Conditions
- Chronic Rhinosinusitis Without Polyps
- Interventions
- Exosomes, Azelastine, and Interferon alpha-2b; Azelastine and Interferon alpha-2b; Placebo Gel Matrix
- Study type
- INTERVENTIONAL
- Phase
- Early phase 1
- Registry status
- Not yet recruiting
- Start
- 2026-07-01
- Completion
- 2027-06-30
- Enrolment
- 108
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Rhinosinusitis Without PolypsInterventionExosomes, Azelastine, and Interferon alpha-2b; Azelastine and Interferon alpha-2b; Placebo Gel MatrixPhaseEarly phase 1Registry statusNot yet recruitingDymista in Chinese Adolescents
NCT07597473 · start 2026-05-08
Registered record
- Registry ID
- NCT07597473
- Conditions
- Allergic Rhinitis Due to Allergens
- Interventions
- Treatment with 137 µg azelastine hydrochloride and 50 μg of fluticasone propionate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2026-05-08
- Completion
- 2027-03
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic Rhinitis Due to AllergensInterventionTreatment with 137 µg azelastine hydrochloride and 50 μg of fluticasone propionatePhasePhase 4Registry statusRecruitingAzelastine Allergen Chamber - Onset of Action Study
NCT06126952 · start 2023-10-30
Registered record
- Registry ID
- NCT06126952
- Conditions
- Seasonal Allergic Rhinitis
- Interventions
- Treatment A: Azelastine hydrochloride 0.15% nasal spray (Azelair); Treatment B: Placebo (Azelastine 0.15% vehicle) nasal spray; Treatment C: Ryaltris (Active Control) - mometasone furoate monohydrate and olopatadine hydrochloride nasal spray
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2023-10-30
- Completion
- 2024-03-18
- Enrolment
- 84
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic RhinitisInterventionTreatment A: Azelastine hydrochloride 0.15% nasal spray (Azelair); Treatment B: Placebo (Azelastine 0.15% vehicle) nasal spray; Treatment C: Ryaltris (Active Control) - mometasone furoate monohydrate and olopatadine hydrochloride nasal sprayPhasePhase 2Registry statusCompletedStudy to Compare the Pharmacokinetics of Fixed-Dose Combination of Mometasone + Azelastine Nasal Spray to Mometasone and Azelastine Nasal Sprays in Adolescents and Young Adults With Seasonal Allergic Rhinitis
NCT05887843 · start 2023-06-08
Registered record
- Registry ID
- NCT05887843
- Conditions
- Seasonal Allergic Rhinitis
- Interventions
- Mometasone + Azelastine; Mometasone Furoate; Azelastine Hydrochloride
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Terminated
- Start
- 2023-06-08
- Completion
- 2023-09-08
- Enrolment
- 38
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic RhinitisInterventionMometasone + Azelastine; Mometasone Furoate; Azelastine HydrochloridePhasePhase 1Registry statusTerminatedClinical and Biological Evaluation of NAAGA Versus Azelastine Eye Drops in Allergic Subjects With Tear Film Dysfunction
NCT06800274 · start 2023-04-21
Registered record
- Registry ID
- NCT06800274
- Conditions
- Allergic Conjunctivitis; Dry Eye Disease (DED)
- Interventions
- NAAGA (N-acetyl-aspartyl-glutamate) 49 mg/mL; azelastine hydrochloride 0.05%
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2023-04-21
- Completion
- 2024-03-28
- Enrolment
- 134
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic Conjunctivitis; Dry Eye Disease (DED)InterventionNAAGA (N-acetyl-aspartyl-glutamate) 49 mg/mL; azelastine hydrochloride 0.05%PhasePhase 4Registry statusCompletedBioequivalence Study of Azelastine Hydrochloride/ Fluticasone Propionate 137 Microgram/50 Microgram Nasal Spray and Dymista Nasal Spray
NCT06180083 · start 2023-03-24
Registered record
- Registry ID
- NCT06180083
- Conditions
- Seasonal Allergic Rhinitis; Perennial Allergic Rhinitis
- Interventions
- Azelastine Hydrochloride/ Fluticasone propionate nasal spray; 'DYMISTA' NASAL SPRAY
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2023-03-24
- Completion
- 2023-07-05
- Enrolment
- 56
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic Rhinitis; Perennial Allergic RhinitisInterventionAzelastine Hydrochloride/ Fluticasone propionate nasal spray; 'DYMISTA' NASAL SPRAYPhasePhase 1Registry statusCompletedA Study to Evaluate the Efficacy and Safety of Epinastine Hydrochloride Eye Drops in the Treatment of Chinese Seasonal Allergic Conjunctivitis Patients
NCT06212973 · start 2023-03-13
Registered record
- Registry ID
- NCT06212973
- Conditions
- Seasonal Allergic Conjunctivitis
- Interventions
- Epinastine Hcl Oph Soln+Simulating Azelastine Hcl Oph Soln; Azelastine Hcl Oph Sol+Simulating Epinastine Hcl Oph Soln
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2023-03-13
- Completion
- 2023-11-02
- Enrolment
- 266
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic ConjunctivitisInterventionEpinastine Hcl Oph Soln+Simulating Azelastine Hcl Oph Soln; Azelastine Hcl Oph Sol+Simulating Epinastine Hcl Oph SolnPhasePhase 3Registry statusCompletedINTRANASAL FLUTICASONE VERSUS FLUTICASONE-AZELASTINE COMBINATION
NCT07415278 · start 2022-12-01
Registered record
- Registry ID
- NCT07415278
- Conditions
- Allergic Rhinitis
- Interventions
- Fluticasone propionate nasal spray; Fluticasone propionate-azelastine nasal spray
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Active not recruiting
- Start
- 2022-12-01
- Completion
- 2026-10-30
- Enrolment
- 61
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic RhinitisInterventionFluticasone propionate nasal spray; Fluticasone propionate-azelastine nasal sprayPhasePhase 4Registry statusActive not recruitingProspective, Randomized, Multinational, Multicenter, Double-blind, Placebo and Active Controlled Trial in 4 Parallel-groups of Patients Suffering From Seasonal Allergic Rhinitis
NCT05311475 · start 2022-04-04
Registered record
- Registry ID
- NCT05311475
- Conditions
- Seasonal Allergic Rhinitis
- Interventions
- Mometasone; Azelastine; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-04-04
- Completion
- 2023-06-20
- Enrolment
- 669
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic RhinitisInterventionMometasone; Azelastine; PlaceboPhasePhase 3Registry statusCompletedObservational Study to Evaluate the Actual Use and Effectiveness of Dymista® Nasal Spray in Asian Patients
NCT05158972 · start 2021-10-27
Registered record
- Registry ID
- NCT05158972
- Conditions
- Allergic Rhinitis
- Interventions
- Dymista
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2021-10-27
- Completion
- 2023-10-24
- Enrolment
- 924
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic RhinitisInterventionDymistaPhaseNot recordedRegistry statusCompletedEfficacy and Safety Study of AI201901 in Allergic Rhinitis Patients
NCT04729517 · start 2021-04-20
Registered record
- Registry ID
- NCT04729517
- Conditions
- Allergic Rhinitis Due to Allergens
- Interventions
- AI201901; Azelastine Hydrochloride
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2021-04-20
- Completion
- 2023-05-02
- Enrolment
- 210
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic Rhinitis Due to AllergensInterventionAI201901; Azelastine HydrochloridePhasePhase 3Registry statusCompletedTo Investigate Drug-drug Interaction and Relative Bioavailability Between the FDC AzelastineHCL/Beclomethasone Dipropionate Nasal Spray, & Beclomethasone Dipropionate Nasal Spray in the Test Vehicle, and RinoClenil® Nasal Spray
NCT04817800 · start 2021-03-25
Registered record
- Registry ID
- NCT04817800
- Conditions
- Seasonal Allergic Rhinitis
- Interventions
- 140/100 μg Azelastine hydrochloride/Beclomethasone Dipropionate)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1 / Phase 2
- Registry status
- Completed
- Start
- 2021-03-25
- Completion
- 2021-04-10
- Enrolment
- 48
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic RhinitisIntervention140/100 μg Azelastine hydrochloride/Beclomethasone Dipropionate)PhasePhase 1 / Phase 2Registry statusCompletedAllergic Rhinitis Combination Pharmacotherapy Efficacy Study
NCT04601324 · start 2020-12-15
Registered record
- Registry ID
- NCT04601324
- Conditions
- Allergic Rhinitis
- Interventions
- Fluticasone Propionate; Azelastine hydrochloride and fluticasone propionate; Rupatadine
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2020-12-15
- Completion
- 2021-07-01
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAllergic RhinitisInterventionFluticasone Propionate; Azelastine hydrochloride and fluticasone propionate; RupatadinePhasePhase 4Registry statusWithdrawnDymista Allergen Chamber - Onset of Action Study
NCT04652245 · start 2020-12-14
Registered record
- Registry ID
- NCT04652245
- Conditions
- Seasonal Allergic Rhinitis
- Interventions
- Treatment A (Dymista): Fixed drug combination of azelastine hydrochloride and fluticasone propionate nasal spray at Visit 3; Treatment B (Placebo): Nasal spray with no active dose (Dymista vehicle) at Visit 5; Treatment A (Dymista): Fixed drug combination of azelastine hydrochloride and fluticasone propionate nasal spray at Visit 5; Treatment B (Placebo): Nasal spray with no active dose (Dymista vehicle) at Visit 3
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2020-12-14
- Completion
- 2021-12-13
- Enrolment
- 216
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSeasonal Allergic RhinitisInterventionTreatment A (Dymista): Fixed drug combination of azelastine hydrochloride and fluticasone propionate nasal spray at Visit 3; Treatment B (Placebo): Nasal spray with no active dose (Dymista vehicle) at Visit 5; Treatment A (Dymista): Fixed drug combination of azelastine hydrochloride and fluticasone propionate nasal spray at Visit 5; Treatment B (Placebo): Nasal spray with no active dose (Dymista vehicle) at Visit 3PhasePhase 4Registry statusCompleted