Tolvaptan
FDA-approved product (tablet, oral), marketed as Jynarque, Samsca, Tolvaptan.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Autosomal dominant polycystic kidney disease
- Cardiovascular disease
- Congestive heart failure
- Heart failure
- Hyponatremia
- Inappropriate ADH syndrome
- Polycystic Kidney Disease
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Vasopressin antagonists
- FDA pharmacologic class
- Vasopressin V2 Receptor Antagonist 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 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- MRSA60.8% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli44.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- K. pneumoniae19.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis70.0% 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 Tolvaptan 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.
Bempedoic Acid Therapy for Polycystic Kidney Disease
NCT07282821 · start 2026-09-21
Registered record
- Registry ID
- NCT07282821
- Conditions
- ADPKD (Autosomal Dominant Polycystic Kidney Disease)
- Interventions
- Bempedoic Acid 180 MG Oral Tablet; Placebo Capsule(s)
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Not yet recruiting
- Start
- 2026-09-21
- Completion
- 2030-03-31
- Enrolment
- 120
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionADPKD (Autosomal Dominant Polycystic Kidney Disease)InterventionBempedoic Acid 180 MG Oral Tablet; Placebo Capsule(s)PhasePhase 2Registry statusNot yet recruitingA Study to See if Tolvaptan is Safe in Infants and Children Who at Enrollment Are 28 Days to Less Than 18 Years Old With Autosomal Recessive Polycystic Kidney Disease (ARPKD)
NCT04782258 · start 2023-01-23
Registered record
- Registry ID
- NCT04782258
- Conditions
- Autosomal Recessive Polycystic Kidney (ARPKD)
- Interventions
- Tolvaptan Suspension; Tolvaptan Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Recruiting
- Start
- 2023-01-23
- Completion
- 2028-08-14
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Recessive Polycystic Kidney (ARPKD)InterventionTolvaptan Suspension; Tolvaptan TabletsPhasePhase 3Registry statusRecruitingTolvaptan add-on Therapy to Overcome Loop Diuretic Resistance in Acute Heart Failure With Renal Dysfunction
NCT04331132 · start 2021-12-01
Registered record
- Registry ID
- NCT04331132
- Conditions
- Acute Heart Failure
- Interventions
- Tolvaptan 15 MG
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2021-12-01
- Completion
- 2023-07-26
- Enrolment
- 128
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Heart FailureInterventionTolvaptan 15 MGPhaseNot applicableRegistry statusUnknownPostoperative Tolvaptan Use in Left Ventricular Assist Device Implantation Patients
NCT05408104 · start 2019-03-28
Registered record
- Registry ID
- NCT05408104
- Conditions
- Heart Failure; Heart Assist Device; Hyponatremic
- Interventions
- tolvaptan
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2019-03-28
- Completion
- 2022-05-01
- Enrolment
- 28
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart Failure; Heart Assist Device; HyponatremicInterventiontolvaptanPhaseNot recordedRegistry statusCompletedEfficacy and Safety Trial of OPC-61815 Injection Compared With Tolvaptan 15-mg Tablet in Patients With Congestive Heart Failure
NCT03772041 · start 2019-01-16
Registered record
- Registry ID
- NCT03772041
- Conditions
- Congestive Heart Failure
- Interventions
- OPC-61815; Tolvaptan Tab 15 MG
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2019-01-16
- Completion
- 2020-07-29
- Enrolment
- 294
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCongestive Heart FailureInterventionOPC-61815; Tolvaptan Tab 15 MGPhasePhase 3Registry statusCompletedTolvaptan-Octreotide LAR Combination in ADPKD
NCT03541447 · start 2018-12-12
Registered record
- Registry ID
- NCT03541447
- Conditions
- Autosomal Dominant Polycystic Kidney Disease
- Interventions
- Tolvaptan; Octreotide LAR; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2018-12-12
- Completion
- 2021-12-23
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic Kidney DiseaseInterventionTolvaptan; Octreotide LAR; PlaceboPhasePhase 2Registry statusCompletedSubacute Effect of Tolvaptan on Total Kidney Volume in Adult Patients With Autosomal Dominant Polycystic Kidney Disease
NCT03596957 · start 2018-09-12
Registered record
- Registry ID
- NCT03596957
- Conditions
- Autosomal Dominant Polycystic Kidney
- Interventions
- Tolvaptan
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2018-09-12
- Completion
- 2020-04
- Enrolment
- 90
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic KidneyInterventionTolvaptanPhasePhase 4Registry statusUnknownA Multicenter Trial to Investigate the Efficacy and Safety of Tolvaptan in Patients With Hyponatremia in SIADH
NCT03048747 · start 2017-03-02
Registered record
- Registry ID
- NCT03048747
- Conditions
- Syndrome of Inappropriate Antidiuretic Hormone Secretion
- Interventions
- Tolvaptan Oral Tablet
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2017-03-02
- Completion
- 2019-03-19
- Enrolment
- 16
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSyndrome of Inappropriate Antidiuretic Hormone SecretionInterventionTolvaptan Oral TabletPhasePhase 3Registry statusCompletedA Study of OPC-41061 Orally Disintegrating (OD) Tablets Using 2 Different Formulations and 2 Dosing Regimens in Healthy Adult Male Subjects
NCT02994394 · start 2017-01-06
Registered record
- Registry ID
- NCT02994394
- Conditions
- Healthy Adult Male
- Interventions
- OPC-41061
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2017-01-06
- Completion
- 2017-02-28
- Enrolment
- 84
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy Adult MaleInterventionOPC-41061PhasePhase 1Registry statusCompletedSamsca PMS in ADPKD Patients
NCT03406286 · start 2016-07-19
Registered record
- Registry ID
- NCT03406286
- Conditions
- Safety
- Interventions
- Tolvaptan
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2016-07-19
- Completion
- 2024-12
- Enrolment
- 2,067
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSafetyInterventionTolvaptanPhaseNot recordedRegistry statusCompletedCanadian Medical Assessment of JINARC™ Outcomes Registry
NCT02925221 · start 2016-02-26
Registered record
- Registry ID
- NCT02925221
- Conditions
- Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2016-02-26
- Completion
- 2025-12-31
- Enrolment
- 530
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic Kidney Disease (ADPKD)InterventionNot recordedPhaseNot recordedRegistry statusCompletedComparison of Oral or Intravenous Thiazides vs Tolvaptan in Diuretic Resistant Decompensated Heart Failure
NCT02606253 · start 2016-02
Registered record
- Registry ID
- NCT02606253
- Conditions
- Heart Failure
- Interventions
- tolvaptan; Chlorothiazide; Metolazone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2016-02
- Completion
- 2018-10-31
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart FailureInterventiontolvaptan; Chlorothiazide; MetolazonePhasePhase 4Registry statusCompletedAiDing Diuresis wIth Tolvaptan (ADD-IT)
NCT02646540 · start 2016-01
Registered record
- Registry ID
- NCT02646540
- Conditions
- Cardiomyopathy; Congestive Heart Failure
- Interventions
- Tolvaptan 30 mg + IV Diuretics; Metolazone 5 mg + IV Diuretics; 2.5 times the Diuretics Dose
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2016-01
- Completion
- 2018-12-30
- Enrolment
- 14
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCardiomyopathy; Congestive Heart FailureInterventionTolvaptan 30 mg + IV Diuretics; Metolazone 5 mg + IV Diuretics; 2.5 times the Diuretics DosePhasePhase 1Registry statusCompletedA Trial of Tolvaptan in Children and Adolescent Subjects With Euvolemic and Hypervolemic Hyponatremia
NCT02442674 · start 2015-11
Registered record
- Registry ID
- NCT02442674
- Conditions
- Hyponatremia
- Interventions
- Tolvaptan; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Withdrawn
- Start
- 2015-11
- Completion
- 2017-06-22
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHyponatremiaInterventionTolvaptan; PlaceboPhasePhase 3Registry statusWithdrawnAn Observational Study on Real-world Use and Outcomes of Patients Treated With Tolvaptan for Hyponatraemia Due to SIADH
NCT02545101 · start 2015-11
Registered record
- Registry ID
- NCT02545101
- Conditions
- Hyponatremia; Syndrome of Inappropriate ADH (SIADH) Secretion
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2015-11
- Completion
- 2016-04
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHyponatremia; Syndrome of Inappropriate ADH (SIADH) SecretionInterventionNot recordedPhaseNot recordedRegistry statusCompleted