Chlorthalidone
FDA-approved product (tablet, oral), marketed as Chlorthalidone, Hemiclor, Hygroton and 1 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 2 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Angina pectoris
- Cardiovascular disease
- Chronic kidney disease
- Congestive heart failure
- Glomerulonephritis
- Heart failure
- Hypertension
- Nephrotic syndrome
- Preeclampsia
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Sulfonamides, plain
- FDA pharmacologic class
- Thiazide-like Diuretic 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- MRSA51.5% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli21.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae14.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis68.8% 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 Chlorthalidone 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.
LOw DosE Spironolactone, chlorThAlidone oR Combination in CKD Trial
NCT07645300 · start 2026-10-01
Registered record
- Registry ID
- NCT07645300
- Conditions
- Hypertension Treated With Antihypertensive Drugs; Chronic Kidney Disease, 3B and 4
- Interventions
- phase 2A Chlorthalidone; phase 2A Spironolactone; phase 2A Chlorthalidone + Spironolactone; phase 2B Chlorthalidone LD + Spironolactone LD
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-10-01
- Completion
- 2032-06-30
- Enrolment
- 160
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension Treated With Antihypertensive Drugs; Chronic Kidney Disease, 3B and 4Interventionphase 2A Chlorthalidone; phase 2A Spironolactone; phase 2A Chlorthalidone + Spironolactone; phase 2B Chlorthalidone LD + Spironolactone LDPhasePhase 2Registry statusNot yet recruitingCardiac Effects of Mineralocorticoid Receptor Antagonism After Preeclampsia
NCT07238400 · start 2026-03-20
Registered record
- Registry ID
- NCT07238400
- Conditions
- Hypertension
- Interventions
- Eplerenone 100 mg daily; Chlorthalidone 25 mg daily; Potassium Placebo; Potassium Chloride
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2026-03-20
- Completion
- 2029-03-30
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionEplerenone 100 mg daily; Chlorthalidone 25 mg daily; Potassium Placebo; Potassium ChloridePhasePhase 2Registry statusRecruitingCaOx Stone Prevention
NCT07225764 · start 2025-10-23
Registered record
- Registry ID
- NCT07225764
- Conditions
- Kidney Stones
- Interventions
- Chlorthalidone; Low oxalate diet
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2025-10-23
- Completion
- 2027-12-31
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionKidney StonesInterventionChlorthalidone; Low oxalate dietPhasePhase 4Registry statusRecruitingArterial Stiffness and Blood Pressure
NCT06495710 · start 2025-05-01
Registered record
- Registry ID
- NCT06495710
- Conditions
- Hypertension; Vascular Stiffness; Aging
- Interventions
- Blood pressure treatment algorithm
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2025-05-01
- Completion
- 2028-12-31
- Enrolment
- 228
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Vascular Stiffness; AgingInterventionBlood pressure treatment algorithmPhaseNot applicableRegistry statusRecruitingMineralocorticoid Receptor, Coronary Microvascular Function, and Cardiac Efficiency in Hypertension
NCT05593055 · start 2023-08-25
Registered record
- Registry ID
- NCT05593055
- Conditions
- Hypertension; Left Ventricular Hypertrophy
- Interventions
- Eplerenone; Chlorthalidone; Potassium
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2023-08-25
- Completion
- 2027-12-31
- Enrolment
- 75
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Left Ventricular HypertrophyInterventionEplerenone; Chlorthalidone; PotassiumPhasePhase 4Registry statusRecruitingSkin Sodium and Salt Sensitivity of Blood Pressure
NCT05976438 · start 2023-08
Registered record
- Registry ID
- NCT05976438
- Conditions
- Hypertension
- Interventions
- Amlodipine; Chlortalidone
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2023-08
- Completion
- 2024-12
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionAmlodipine; ChlortalidonePhaseNot applicableRegistry statusUnknownDiuretic Use in Hemodialysis Patients With Residual Renal Function
NCT05915286 · start 2023-05-29
Registered record
- Registry ID
- NCT05915286
- Conditions
- End Stage Renal Disease on Dialysis
- Interventions
- Furosemide; Chlorthalidone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2023-05-29
- Completion
- 2025-02-21
- Enrolment
- 2
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEnd Stage Renal Disease on DialysisInterventionFurosemide; ChlorthalidonePhasePhase 4Registry statusTerminatedA Multicenter, Randomized, Double-Blind Phase 3 Trial of KDF1901 in Patients With Essential Hypertension
NCT07116863 · start 2022-06-21
Registered record
- Registry ID
- NCT07116863
- Conditions
- Essential Hypertension
- Interventions
- KDF1901-R0; KDF1901-L; KDF1901; KDF1901-R1
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2022-06-21
- Completion
- 2024-09-13
- Enrolment
- 286
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEssential HypertensionInterventionKDF1901-R0; KDF1901-L; KDF1901; KDF1901-R1PhasePhase 3Registry statusCompletedDiuretic Treatment in Acute Heart Failure With Volume Overload Guided by Serial Spot Urine Sodium Assessment
NCT05411991 · start 2022-06-12
Registered record
- Registry ID
- NCT05411991
- Conditions
- Acute Heart Failure; Diuretics Drug Reactions
- Interventions
- UNa measurement after intravenous loop diuretic bolus; Intravenous acetazolamide 500 mg OD; Intravenous bumetanide TID; Oral chlorthalidone OD; Intravenous canrenoate 200 mg OD; Maintenance infusion; Oral potassium supplements; Intravenous hypertonic saline; Switch to oral diuretic therapy; Usual AHF care
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2022-06-12
- Completion
- 2024-07-01
- Enrolment
- 107
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Heart Failure; Diuretics Drug ReactionsInterventionUNa measurement after intravenous loop diuretic bolus; Intravenous acetazolamide 500 mg OD; Intravenous bumetanide TID; Oral chlorthalidone OD +6 morePhasePhase 4Registry statusCompletedStudy to Evaluate the Efficacy and Safety of TEL/AML/CTD in Elderly Patients with Essential Hypertension
NCT06282549 · start 2022-06-08
Registered record
- Registry ID
- NCT06282549
- Conditions
- Essential Hypertension
- Interventions
- Telmisartan/Amlodipine/Chlorthalidone(Truset)
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Active not recruiting
- Start
- 2022-06-08
- Completion
- 2027-03-31
- Enrolment
- 1,219
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEssential HypertensionInterventionTelmisartan/Amlodipine/Chlorthalidone(Truset)PhaseNot recordedRegistry statusActive not recruitingHypertension in Young Adults Trial
NCT05370599 · start 2022-04-15
Registered record
- Registry ID
- NCT05370599
- Conditions
- Hypertension
- Interventions
- Anti-hypertensive agent: amlodipine; Anti-hypertensive agent: Chlorthalidone; Anti-hypertensive agent: Losartan; Home BP monitoring with cuffed device; Home BP monitoring with cuffed device + BP patch; Home BP monitoring with cuffed device + BP watch
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2022-04-15
- Completion
- 2026-01-07
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionAnti-hypertensive agent: amlodipine; Anti-hypertensive agent: Chlorthalidone; Anti-hypertensive agent: Losartan; Home BP monitoring with cuffed device +2 morePhasePhase 2Registry statusTerminatedSpironolactone in CKD Enabled by Chlorthalidone: PILOT
NCT05222191 · start 2022-02-01
Registered record
- Registry ID
- NCT05222191
- Conditions
- Renal Insufficiency; Chronic Hypertension
- Interventions
- Spironolactone; Chlorthalidone; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Unknown
- Start
- 2022-02-01
- Completion
- 2023-12-12
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRenal Insufficiency; Chronic HypertensionInterventionSpironolactone; Chlorthalidone; PlaceboPhasePhase 2Registry statusUnknownOPtimizing Technology to Improve Medication Adherence and BP Control (OPTIMA-BP)
NCT05293756 · start 2021-02-14
Registered record
- Registry ID
- NCT05293756
- Conditions
- Hypertension; Self-Management; Technology; Quality of Life
- Interventions
- OPTIMA-BP Intervention
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Recruiting
- Start
- 2021-02-14
- Completion
- 2027-05-31
- Enrolment
- 208
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Self-Management; Technology; Quality of LifeInterventionOPTIMA-BP InterventionPhaseNot applicableRegistry statusRecruitingClinical Efficacy and Safety Evaluation of HCP1904-2 in Essential Hypertension Patients
NCT04830449 · start 2020-10-29
Registered record
- Registry ID
- NCT04830449
- Conditions
- Hypertension
- Interventions
- HCP1904-2; RLD2001-2
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2020-10-29
- Completion
- 2021-08-24
- Enrolment
- 122
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionHCP1904-2; RLD2001-2PhasePhase 3Registry statusCompletedA Study for PMS of AZL-M/CLD FDC in the Treatment of Participants With Essential HTN in South Korea
NCT04470830 · start 2019-09-11
Registered record
- Registry ID
- NCT04470830
- Conditions
- Essential Hypertension
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2019-09-11
- Completion
- 2023-05-25
- Enrolment
- 718
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEssential HypertensionInterventionNot recordedPhaseNot recordedRegistry statusCompleted