Estazolam
FDA-approved product (tablet, oral), marketed as Estazolam, Prosom.
- Registered studies
- 12
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBL- WHO therapeutic group
- Benzodiazepine derivatives
- FDA pharmacologic class
- Benzodiazepine 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 M. tuberculosis and MRSA. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA50.4% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli29.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae16.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis60.6% 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
12registered 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 Estazolam 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.
Compound Ciwujia Granules in the Treatment of Insomnia
NCT07306494 · start 2026-01
Registered record
- Registry ID
- NCT07306494
- Conditions
- Insomnia Disorder
- Interventions
- Compound Ciwujia Granules group; Estazolam; Compound Ciwujia Granules and estazolam
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Not yet recruiting
- Start
- 2026-01
- Completion
- 2028-06
- Enrolment
- 1,200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionInsomnia DisorderInterventionCompound Ciwujia Granules group; Estazolam; Compound Ciwujia Granules and estazolamPhasePhase 4Registry statusNot yet recruitingEfficacy of Auricular Pressure Beans with Electroacupuncture and Estazolam Treating Insomnia Caused by Cancer
NCT06859190 · start 2025-03-01
Registered record
- Registry ID
- NCT06859190
- Conditions
- Cancer; Insomnia
- Interventions
- estazolam 1-2 mg; Auricular pressure bean combined with electroacupuncture
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2025-03-01
- Completion
- 2026-12-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCancer; InsomniaInterventionestazolam 1-2 mg; Auricular pressure bean combined with electroacupuncturePhasePhase 3Registry statusRecruitingA Randomized Controlled Trial of Auricular Acupressure in Treating Estazolam-dependent Insomnia
NCT06258226 · start 2024-07-01
Registered record
- Registry ID
- NCT06258226
- Conditions
- Estazolam-dependent Insomnia
- Interventions
- Conventional dosage reduction; Auricular acupressure; Sham auricular acupressure
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2024-07-01
- Completion
- 2025-06-30
- Enrolment
- 108
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEstazolam-dependent InsomniaInterventionConventional dosage reduction; Auricular acupressure; Sham auricular acupressurePhaseNot applicableRegistry statusUnknown"Chou's Tiaoshen" Acupoints for Short-term Insomnia.
NCT06212934 · start 2024-03-01
Registered record
- Registry ID
- NCT06212934
- Conditions
- Short-term Insomnia
- Interventions
- Acupuncture; Estazolam
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2024-03-01
- Completion
- 2025-05-01
- Enrolment
- 96
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionShort-term InsomniaInterventionAcupuncture; EstazolamPhaseNot applicableRegistry statusUnknownTreatment of Chronic Insomnia According to Yin Yang Theory and Its Correlation With Circadian Rhythm
NCT05452577 · start 2021-01-22
Registered record
- Registry ID
- NCT05452577
- Conditions
- Chronic Insomnia; Circadian Rhythm; Traditional Chinese Medicine
- Interventions
- Suanzaoren Decoction and Huanglian Wendan Decoction; Estazolam 1Mg Tab
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2021-01-22
- Completion
- 2023-05-30
- Enrolment
- 187
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChronic Insomnia; Circadian Rhythm; Traditional Chinese MedicineInterventionSuanzaoren Decoction and Huanglian Wendan Decoction; Estazolam 1Mg TabPhaseNot applicableRegistry statusCompletedObservation on the Effect of Auricular Acupoint Pressing on Insomnia and Adverse Events in MHD
NCT03997058 · start 2019-03-01
Registered record
- Registry ID
- NCT03997058
- Conditions
- Renal Dialysis; Sleep Initiation and Maintenance Disorders
- Interventions
- Auricular point pressure therapy; Oral estazolam medication
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2019-03-01
- Completion
- 2021-01-01
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRenal Dialysis; Sleep Initiation and Maintenance DisordersInterventionAuricular point pressure therapy; Oral estazolam medicationPhasePhase 4Registry statusUnknownEffects of Dexmedetomidine on Cognitive Outcome and Brain Injury Markers
NCT03585452 · start 2018-08-01
Registered record
- Registry ID
- NCT03585452
- Conditions
- Cognitive Dysfunction
- Interventions
- Dexmedetomidine Infusion; Propofol based general anesthesia
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2018-08-01
- Completion
- 2019-03-31
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCognitive DysfunctionInterventionDexmedetomidine Infusion; Propofol based general anesthesiaPhaseNot applicableRegistry statusCompletedRisk and Benefit Assessment of Hypnotic Agents for Sleep Disorders Among Elderly
NCT02648776 · start 2016-01
Registered record
- Registry ID
- NCT02648776
- Conditions
- Sleep Disorders
- Interventions
- Exposure to sedative-hypnotic drugs
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2016-01
- Completion
- 2018-12
- Enrolment
- 1,400
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSleep DisordersInterventionExposure to sedative-hypnotic drugsPhaseNot recordedRegistry statusUnknownSunitinib or Cediranib for Alveolar Soft Part Sarcoma
NCT01391962 · start 2011-07-18
Registered record
- Registry ID
- NCT01391962
- Conditions
- Sarcoma, Alveolar Soft Part
- Interventions
- Cediranib; Sunitinib; Prochlorperazine; Promethazine; Benzodiazepine; Filgrastim; Sargramostim; Lomotil; Loperamide; Vitamin B6; Aquaphor; Acetaminophen; Levothyroxine; Warfarin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2011-07-18
- Completion
- 2026-01-16
- Enrolment
- 34
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSarcoma, Alveolar Soft PartInterventionCediranib; Sunitinib; Prochlorperazine; Promethazine +10 morePhasePhase 2Registry statusCompletedA Study to Evaluate Efficacy and Safety of Zolpidem Modified Release Formulation in Insomnia Patients
NCT00956319 · start 2009-05
Registered record
- Registry ID
- NCT00956319
- Conditions
- Sleep Initiation and Maintenance Disorders; Primary Insomnia
- Interventions
- Zolpidem MR; Estazolam
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2009-05
- Completion
- 2010-11
- Enrolment
- 42
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSleep Initiation and Maintenance Disorders; Primary InsomniaInterventionZolpidem MR; EstazolamPhasePhase 4Registry statusCompletedEffects of Discontinuation of Benzodiazepine-derivative Hypnotics on Cognitive and Motor Functions in Elderly Persons
NCT00707915 · start 2008-01
Registered record
- Registry ID
- NCT00707915
- Conditions
- Adverse Effects
- Interventions
- Drug: Benzodiazepine (listed out below)
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-01
- Completion
- 2010-07
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAdverse EffectsInterventionDrug: Benzodiazepine (listed out below)PhasePhase 4Registry statusCompletedRandomised, Double-blind Study to Investigate the Safety and Efficacy of Brotizolam in Insomnia Outpatients.
NCT00347295 · start 2006-06
Registered record
- Registry ID
- NCT00347295
- Conditions
- Sleep Initiation and Maintenance Disorders
- Interventions
- Brotizolam; Estazolam
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2006-06
- Completion
- 2007-01
- Enrolment
- 253
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSleep Initiation and Maintenance DisordersInterventionBrotizolam; EstazolamPhasePhase 3Registry statusCompleted