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      Effect of renal function on the pharmacokinetics of LCZ696 (sacubitril/valsartan), an angiotensin receptor neprilysin inhibitor.

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          Abstract

          LCZ696 (sacubitril/valsartan), an angiotensin receptor neprilysin inhibitor, is indicated for chronic heart failure (HF) and reduced ejection fraction (HFrEF) to reduce the risk of cardiovascular death and hospitalization for HF. Following oral administration, LCZ696 provides systemic exposure to valsartan and sacubitril (a prodrug), and its metabolite sacubitrilat (the active neprilysin inhibitor, formerly named as LBQ657), which is eliminated primarily via renal route. Since renal dysfunction is a common comorbidity in patients with HF, two open-label studies assessing the effect of mild, moderate, and severe renal impairment were conducted.

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          Author and article information

          Journal
          Eur. J. Clin. Pharmacol.
          European journal of clinical pharmacology
          Springer Nature America, Inc
          1432-1041
          0031-6970
          Sep 2016
          : 72
          : 9
          Affiliations
          [1 ] Drug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, East Hanover, NJ, USA. surya.ayalasomayajula@novartis.com.
          [2 ] Translational Medicine, Clinical Pharmacology and Profiling, Novartis Pharma AG, Basel, Switzerland.
          [3 ] Drug Metabolism and Pharmacokinetics, Novartis Institutes for BioMedical Research, East Hanover, NJ, USA.
          [4 ] Novartis Healthcare Pvt Ltd, Hyderabad, Telangana, India.
          Article
          10.1007/s00228-016-2072-7
          10.1007/s00228-016-2072-7
          27230850
          b4f303a5-37ef-4058-a9d9-9dcfb3613e78
          History

          LCZ696,Angiotensin receptor neprilysin inhibitor,Pharmacokinetics,Renal impairment,Sacubitril,Valsartan

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