CLINICAL TRIALS PROFILE FOR SACUBITRIL; VALSARTAN
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All Clinical Trials for sacubitril; valsartan
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT01920711 ↗ | Efficacy and Safety of LCZ696 Compared to Valsartan, on Morbidity and Mortality in Heart Failure Patients With Preserved Ejection Fraction | Completed | Novartis Pharmaceuticals | Phase 3 | 2014-07-18 | The purpose of this study was to evaluate the effect of LCZ696 compared to valsartan in the reduction of cardiovascular death and heart failure(HF) hospitalizations in patients with HF with preserved ejection fraction. |
NCT02554890 ↗ | Comparison of Sacubitril/Valsartan Versus Enalapril on Effect on NT-proBNP in Patients Stabilized From an Acute Heart Failure Episode. | Completed | Novartis Pharmaceuticals | Phase 4 | 2016-04-29 | The purpose of this study was to assess the effect of in-hospital initiation of sacubitril/valsartan (LCZ696) vs. enalapril on time averaged proportional change in NT-proBNP in patients who have been stabilized following hospitalization for acute decompensated heart failure (ADHF) and reduced ejection fraction (left ventricular ejection fraction (LVEF) ≤ 40%). |
NCT02636283 ↗ | Use of Entresto Sacubitril/Valsartan for the Treatment of Peripheral Arterial Disease | Terminated | American Heart Association | Phase 2 | 2017-12-31 | This study proposes the use of Entresto (sacubitril/valsartan) to test the effects on pain free walking duration on patients with peripheral arterial disease, a condition caused by decreased blood flow to the muscles in the legs. |
NCT02636283 ↗ | Use of Entresto Sacubitril/Valsartan for the Treatment of Peripheral Arterial Disease | Terminated | University of Minnesota | Phase 2 | 2017-12-31 | This study proposes the use of Entresto (sacubitril/valsartan) to test the effects on pain free walking duration on patients with peripheral arterial disease, a condition caused by decreased blood flow to the muscles in the legs. |
NCT02636283 ↗ | Use of Entresto Sacubitril/Valsartan for the Treatment of Peripheral Arterial Disease | Terminated | University of Minnesota - Clinical and Translational Science Institute | Phase 2 | 2017-12-31 | This study proposes the use of Entresto (sacubitril/valsartan) to test the effects on pain free walking duration on patients with peripheral arterial disease, a condition caused by decreased blood flow to the muscles in the legs. |
NCT02682719 ↗ | Personalised Prospective Comparison of ARni With ArB in Patients With Natriuretic Peptide eLEvation | Active, not recruiting | Novartis Ireland Ltd | Phase 2 | 2015-12-16 | Sacubitril-valsartan, an Angiotensin Receptor Blocker-Neprilysin Inhibitor (ARNI), currently marketed for the management of heart failure, has been shown to reduce cardiovascular morbidity and mortality in stage C heart failure with reduced ejection fraction. In stage C HFpEF, sacubitril-valsartan has also been shown to reduce left atrial volume index measured using echocardiography over a 9 month timeframe. The PARABLE study investigates the hypothesis that sacubitril-valsartan can provide benefits in terms of left atrial structure and function as well as left ventricular structure and function in asymptomatic (stage A/B HFpEF) patients. This is a prospective, randomised, double-blind, double-dummy, phase II study design. The patient population will have hypertension and/or diabetes together with preserved ejection fraction, elevated natriuretic peptide (NP) and abnormal left atrial volume index (LAVI, > 28 mL/m2). |
NCT02682719 ↗ | Personalised Prospective Comparison of ARni With ArB in Patients With Natriuretic Peptide eLEvation | Active, not recruiting | The Heartbeat Trust | Phase 2 | 2015-12-16 | Sacubitril-valsartan, an Angiotensin Receptor Blocker-Neprilysin Inhibitor (ARNI), currently marketed for the management of heart failure, has been shown to reduce cardiovascular morbidity and mortality in stage C heart failure with reduced ejection fraction. In stage C HFpEF, sacubitril-valsartan has also been shown to reduce left atrial volume index measured using echocardiography over a 9 month timeframe. The PARABLE study investigates the hypothesis that sacubitril-valsartan can provide benefits in terms of left atrial structure and function as well as left ventricular structure and function in asymptomatic (stage A/B HFpEF) patients. This is a prospective, randomised, double-blind, double-dummy, phase II study design. The patient population will have hypertension and/or diabetes together with preserved ejection fraction, elevated natriuretic peptide (NP) and abnormal left atrial volume index (LAVI, > 28 mL/m2). |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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