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Last Updated: December 22, 2024

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CLINICAL TRIALS PROFILE FOR KERENDIA


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All Clinical Trials for kerendia

Trial ID Title Status Sponsor Phase Start Date Summary
NCT05814770 ↗ Comparing the Efficacy and Safety of Finerenone and Spironolactone in the Treatment of Primary Aldosteronism Not yet recruiting National Key Research and Development Program of China Phase 4 2023-05-01 Primary aldosteronism (PA) is thought to be the most common secondary endocrine form of hypertension. Compared with patients with essential hypertension with similar blood pressure, patients with PA have significantly higher atrial fibrillation, myocardial infarction, heart failure, stroke, deterioration of renal function and all-cause mortality. Therefore, early and systematic implementation of effective surgical or medical treatment is essential to prevent or reverse the excess vascular events and mortality of these patients. The patients with bilateral PA were mainly treated with mineralocorticoid receptor antagonists (MRAs). The MRA spironolactone is effective at lowering BP and reversing the harmful metabolic consequences, but its use is limited by adverse effects such as gynaecomastia, mastodynia, menstrual abnormalities and impotence due to its agonist activity at the progesterone receptor and antagonist activity at the androgen receptor. Finerenone is claimed to be a more selective blocker of the mineralocorticoid receptor than spironolactone being associated with fewer antiandrogenic side-effects. In this study, we will compare the efficacy, safety and tolerability of finerenone versus spironolactone in patients with hypertension associated with primary aldosteronism.
NCT05814770 ↗ Comparing the Efficacy and Safety of Finerenone and Spironolactone in the Treatment of Primary Aldosteronism Not yet recruiting National Natural Science Foundation of China Phase 4 2023-05-01 Primary aldosteronism (PA) is thought to be the most common secondary endocrine form of hypertension. Compared with patients with essential hypertension with similar blood pressure, patients with PA have significantly higher atrial fibrillation, myocardial infarction, heart failure, stroke, deterioration of renal function and all-cause mortality. Therefore, early and systematic implementation of effective surgical or medical treatment is essential to prevent or reverse the excess vascular events and mortality of these patients. The patients with bilateral PA were mainly treated with mineralocorticoid receptor antagonists (MRAs). The MRA spironolactone is effective at lowering BP and reversing the harmful metabolic consequences, but its use is limited by adverse effects such as gynaecomastia, mastodynia, menstrual abnormalities and impotence due to its agonist activity at the progesterone receptor and antagonist activity at the androgen receptor. Finerenone is claimed to be a more selective blocker of the mineralocorticoid receptor than spironolactone being associated with fewer antiandrogenic side-effects. In this study, we will compare the efficacy, safety and tolerability of finerenone versus spironolactone in patients with hypertension associated with primary aldosteronism.
NCT05814770 ↗ Comparing the Efficacy and Safety of Finerenone and Spironolactone in the Treatment of Primary Aldosteronism Not yet recruiting The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School Phase 4 2023-05-01 Primary aldosteronism (PA) is thought to be the most common secondary endocrine form of hypertension. Compared with patients with essential hypertension with similar blood pressure, patients with PA have significantly higher atrial fibrillation, myocardial infarction, heart failure, stroke, deterioration of renal function and all-cause mortality. Therefore, early and systematic implementation of effective surgical or medical treatment is essential to prevent or reverse the excess vascular events and mortality of these patients. The patients with bilateral PA were mainly treated with mineralocorticoid receptor antagonists (MRAs). The MRA spironolactone is effective at lowering BP and reversing the harmful metabolic consequences, but its use is limited by adverse effects such as gynaecomastia, mastodynia, menstrual abnormalities and impotence due to its agonist activity at the progesterone receptor and antagonist activity at the androgen receptor. Finerenone is claimed to be a more selective blocker of the mineralocorticoid receptor than spironolactone being associated with fewer antiandrogenic side-effects. In this study, we will compare the efficacy, safety and tolerability of finerenone versus spironolactone in patients with hypertension associated with primary aldosteronism.
NCT05887817 ↗ Effects of Finerenone on Vascular Stiffness and Cardiorenal Biomarkers in T2D and CKD (FIVE-STAR) Not yet recruiting Saga University Phase 4 2023-09-01 To evaluate the effects of finerenone on vascular stiffness and cardiorenal biomarkers in patients with type 2 diabetes and chronic kidney disease.
NCT06008197 ↗ A Study to Determine the Efficacy and Safety of Finerenone on Morbidity and Mortality Among Hospitalized Heart Failure Patients Recruiting Bayer Phase 3 2024-01-17 Finerenone will be compared to placebo to determine efficacy and safety of treatment in patients hospitalized with acute decompensated heart failure (HF) and mildly reduced or preserved left ventricular ejection fraction.
NCT06008197 ↗ A Study to Determine the Efficacy and Safety of Finerenone on Morbidity and Mortality Among Hospitalized Heart Failure Patients Recruiting Saint Luke's Hospital of Kansas City Phase 3 2024-01-17 Finerenone will be compared to placebo to determine efficacy and safety of treatment in patients hospitalized with acute decompensated heart failure (HF) and mildly reduced or preserved left ventricular ejection fraction.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for kerendia

Condition Name

Condition Name for kerendia
Intervention Trials
Chronic Kidney Diseases 2
Chronic Kidney Disease Due to Type 2 Diabetes Mellitus 1
Diabetes Mellitus, Type 2 1
Chronic Kidney Disease stage3 1
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Condition MeSH

Condition MeSH for kerendia
Intervention Trials
Kidney Diseases 2
Diabetes Mellitus, Type 2 2
Renal Insufficiency, Chronic 2
Proteinuria 1
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Clinical Trial Locations for kerendia

Trials by Country

Trials by Country for kerendia
Location Trials
United States 4
Japan 1
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Trials by US State

Trials by US State for kerendia
Location Trials
North Carolina 1
Missouri 1
Florida 1
Colorado 1
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Clinical Trial Progress for kerendia

Clinical Trial Phase

Clinical Trial Phase for kerendia
Clinical Trial Phase Trials
Phase 4 3
Phase 3 1
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for kerendia
Clinical Trial Phase Trials
Not yet recruiting 3
Recruiting 2
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Clinical Trial Sponsors for kerendia

Sponsor Name

Sponsor Name for kerendia
Sponsor Trials
Bayer 2
Saint Luke's Hospital of Kansas City 1
Colorado Prevention Center 1
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Sponsor Type

Sponsor Type for kerendia
Sponsor Trials
Other 8
Industry 3
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