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 E. coli, MRSA 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.
- Dolutegravir SodiumExisting use: HIV infection, HIV-1 infection55.9% AI-predicted activityagainst E. coli50+ registered studies
- Desmopressin AcetateExisting use: Central diabetes insipidus, Diabetes insipidus, Enuresis and 5 more55.8% AI-predicted activityagainst E. coli50+ registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia55.8% AI-predicted activityagainst E. coli50+ registered studies
- Cetrorelix AcetateExisting use: Ovulation Inhibition, Positive regulation of ovulation55.7% AI-predicted activityagainst E. coli50+ registered studies
- Setmelanotide AcetateExisting use: Obesity55.6% AI-predicted activityagainst E. coliNo documented evidence found
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more55.6% AI-predicted activityagainst E. coli50+ registered studies
- LurbinectedinExisting use: Cancer, Neoplasm, Small cell lung carcinoma55.4% AI-predicted activityagainst E. coli50+ registered studies
- Ganirelix AcetateExisting use: Female infertility, Positive regulation of ovulation, Reproductive Techniques, Assisted55.4% AI-predicted activityagainst E. coli50+ registered studies
- Icatibant AcetateExisting use: Angioedema, Hereditary angioedema55.2% AI-predicted activityagainst E. coli33 registered studies
- Dihydroergotamine MesylateExisting use: Migraine disorder55.2% AI-predicted activityagainst E. coli21 registered studies
- Triptorelin PamoateExisting use: Central precocious puberty, Metastatic prostate cancer, Neoplasm and 3 more55.2% AI-predicted activityagainst E. coli50+ registered studies
- LypressinExisting use: Vasopressin and analogues55.1% AI-predicted activityagainst E. coli50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
8-Week Study of Tolvaptan Dose Forms in Autosomal Dominant Polycystic Kidney Disease (ADPKD)
NCT01451827 · start 2011-10
Registered record
- Registry ID
- NCT01451827
- Conditions
- Autosomal Dominant Polycystic Kidney Disease
- Interventions
- Tolvaptan MR; Tolvaptan IR; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2011-10
- Completion
- 2013-07
- Enrolment
- 178
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic Kidney DiseaseInterventionTolvaptan MR; Tolvaptan IR; PlaceboPhasePhase 2Registry statusCompletedPhase I Study Multi Dose of 7.5mg Tolvaptan in Health Male
NCT07166887 · start 2011-06-07
Registered record
- Registry ID
- NCT07166887
- Conditions
- Healthy Subjects
- Interventions
- Tolvaptan
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2011-06-07
- Completion
- 2011-07-27
- Enrolment
- 12
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthy SubjectsInterventionTolvaptanPhasePhase 1Registry statusCompletedTolvaptan for In-hospital Hyponatremia
NCT01386372 · start 2011-06
Registered record
- Registry ID
- NCT01386372
- Conditions
- Hyponatremia
- Interventions
- Tolvaptan; Standard therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2011-06
- Completion
- 2012-11
- Enrolment
- 3
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHyponatremiaInterventionTolvaptan; Standard therapyPhasePhase 2Registry statusTerminatedA Study to Investigate the Long-term Safety and Efficacy of Tolvaptan in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD) [Extension of Trial 156-04-251 in Japan]
NCT01280721 · start 2010-11
Registered record
- Registry ID
- NCT01280721
- Conditions
- Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- Interventions
- tolvaptan
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-11
- Completion
- 2014-08
- Enrolment
- 135
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic Kidney Disease (ADPKD)InterventiontolvaptanPhasePhase 3Registry statusCompletedPost-Authorisation Safety Study of Samsca (Tolvaptan) Used in Routine Medical Practice
NCT01228682 · start 2010-10
Registered record
- Registry ID
- NCT01228682
- Conditions
- SIADH; Non-SIADH Hyponatremia; Non-Hyponatremia
- Interventions
- Tolvaptan
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Unknown
- Start
- 2010-10
- Completion
- 2014-04
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSIADH; Non-SIADH Hyponatremia; Non-HyponatremiaInterventionTolvaptanPhaseNot recordedRegistry statusUnknownShort-term Renal Hemodynamic Effects of Tolvaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease (ADPKD)
NCT01336972 · start 2010-10
Registered record
- Registry ID
- NCT01336972
- Conditions
- Autosomal Dominant Polycystic Kidney Disease
- Interventions
- Tolvaptan
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2010-10
- Completion
- 2011-11
- Enrolment
- 29
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic Kidney DiseaseInterventionTolvaptanPhasePhase 2Registry statusCompletedPhase III Study of Tolvaptan Tablet to Treat Cirrhosis Ascites
NCT01349348 · start 2010-10
Registered record
- Registry ID
- NCT01349348
- Conditions
- Ascites; Hepatic Cirrhosis
- Interventions
- Tolvaptan; Tolvaptan; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-10
- Completion
- 2012-07
- Enrolment
- 535
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAscites; Hepatic CirrhosisInterventionTolvaptan; Tolvaptan; placeboPhasePhase 3Registry statusCompletedTolvaptan Extension Study in Participants With ADPKD
NCT01214421 · start 2010-05-26
Registered record
- Registry ID
- NCT01214421
- Conditions
- Autosomal Dominant Polycystic Kidney Disease (ADPKD)
- Interventions
- Tolvaptan
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2010-05-26
- Completion
- 2016-02-29
- Enrolment
- 1,083
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutosomal Dominant Polycystic Kidney Disease (ADPKD)InterventionTolvaptanPhasePhase 3Registry statusCompletedA Trial of OPC-41061 in Patients With Hepatic Edema - Investigation of the Safety of Treatment at 7.5 mg Beyond 7 Days and of the Effect of Dose Escalation to 15 mg
NCT01048788 · start 2009-12
Registered record
- Registry ID
- NCT01048788
- Conditions
- Cirrhosis
- Interventions
- OPC-41061
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-12
- Completion
- 2011-08
- Enrolment
- 51
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosisInterventionOPC-41061PhasePhase 3Registry statusCompletedA Trial to Investigate the Efficacy of OPC-41061 Administered at a Dose of 7.5 mg in Patients With Hepatic Edema
NCT01050530 · start 2009-12
Registered record
- Registry ID
- NCT01050530
- Conditions
- Cirrhosis
- Interventions
- OPC-41061; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2009-12
- Completion
- 2012-02
- Enrolment
- 162
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosisInterventionOPC-41061; PlaceboPhasePhase 3Registry statusCompletedTolvaptan Versus Fluid Restriction in SIADH
NCT04119206 · start 2009-01-01
Registered record
- Registry ID
- NCT04119206
- Conditions
- Hyponatremia; Syndrome of Inappropriate ADH (SIADH) Secretion; Pituitary
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2009-01-01
- Completion
- 2013-12-31
- Enrolment
- 334
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHyponatremia; Syndrome of Inappropriate ADH (SIADH) Secretion; PituitaryInterventionNot recordedPhaseNot recordedRegistry statusCompletedA Dose-defining Study of OPC-41061 in Treatment of Hepatic Edema
NCT00479336 · start 2007-06
Registered record
- Registry ID
- NCT00479336
- Conditions
- Cirrhosis
- Interventions
- OPC-41061 7.5mg; OPC-41061 placebo; OPC-41061 15mg; OPC-41601 30mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2007-06
- Completion
- 2009-01
- Enrolment
- 104
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCirrhosisInterventionOPC-41061 7.5mg; OPC-41061 placebo; OPC-41061 15mg; OPC-41601 30mgPhasePhase 2Registry statusCompletedA Double-blind, Placebo-controlled Study of OPC-41061 in the Treatment of Cardiac Edema (Congestive Heart Failure)
NCT00462670 · start 2007-04
Registered record
- Registry ID
- NCT00462670
- Conditions
- Edema, Cardiac
- Interventions
- OPC-41061(Tolvaptan)
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-04
- Completion
- 2008-10
- Enrolment
- 110
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEdema, CardiacInterventionOPC-41061(Tolvaptan)PhasePhase 3Registry statusCompletedTolvaptan Phase 3 Efficacy and Safety Study in Autosomal Dominant Polycystic Kidney Disease (ADPKD)
NCT00428948 · start 2007-01
Registered record
- Registry ID
- NCT00428948
- Conditions
- Polycystic Kidney Disease, Autosomal Dominant
- Interventions
- Tolvaptan; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2007-01
- Completion
- 2012-01
- Enrolment
- 1,445
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPolycystic Kidney Disease, Autosomal DominantInterventionTolvaptan; PlaceboPhasePhase 3Registry statusCompleteda Phase I PK Study in Healthy Male Subjects. 2 Groups of Healthy Male Subjects
NCT07166796 · start 2006-10-01
Registered record
- Registry ID
- NCT07166796
- Conditions
- Health Subjects
- Interventions
- singe dose 15mg; single dose 30mg; single dose 60mg; single dose 120mg; multi dose 30mg; multi dose 60mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2006-10-01
- Completion
- 2007-01-31
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealth SubjectsInterventionsinge dose 15mg; single dose 30mg; single dose 60mg; single dose 120mg +2 morePhasePhase 1Registry statusCompleted