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Sacubitril

Generic Name
Sacubitril
Brand Names
Entresto
Drug Type
Small Molecule
Chemical Formula
C24H29NO5
CAS Number
149709-62-6
Unique Ingredient Identifier
17ERJ0MKGI
Background

Sacubitril is a prodrug neprilysin inhibitor used in combination with valsartan to reduce the risk of cardiovascular events in patients with chronic heart failure (NYHA Class II-IV) and reduced ejection fraction. It was approved by the FDA after being given the status of priority review for on July 7, 2015.

Sacubitril's active metabolite, LBQ657 inhibits neprilysin, a neutral endopeptidase that would typically cleave natiuretic peptides such as atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and c-type natriuretic peptide (CNP). ANP and BNP are released under atrial and ventricle stress, which activate downstream receptors leading to vasodilation, natriuresis and diuresis. Under normal conditions, neprilysin breaks down other vasodilating peptides and also vasoconstrictors such as angiotensin I and II, endothelin-1 and peptide amyloid beta-protein. Inhibition of neprilysin therefore leads to reduced breakdown and increased concentration of endogenous natriuretic peptides in addition to increased levels of vasoconstricting hormones such as angiotensin II.

Indication

Used in combination with valsartan to reduce the risk of cardiovascular events in patients with chronic heart failure (NYHA Class II-IV) and reduced ejection fraction. It is usually administered in conjunction with other heart failure therapies, in place of an ACE inhibitor or other ARB.

It is also used in combination with valsartan.

Associated Conditions
Cardiovascular Mortality, Heart Failure, Hospitalization due to cardiac failure
Associated Therapies
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Pharmacovigilance of Drug–Drug Interactions with Nirmatrelvir/Ritonavir

NMV/r (Paxlovid™) is an oral antiviral COVID-19 treatment authorized under EUA by the FDA, effective in reducing hospitalizations and deaths in high-risk patients. It inhibits SARS-CoV-2 Mpro, preventing viral replication, and is coadministered with ritonavir to enhance pharmacokinetics. Real-world studies show NMV/r's effectiveness in reducing severe COVID-19 progression. However, ritonavir's inhibition of CYP3A4 and other enzymes can lead to significant drug-drug interactions (DDIs), necessitating careful patient selection and management of concomitant medications. Pfizer's Global SDB reported 966 cases of DDIs, with low reporting rates (0.005%) and mostly nonserious events, though 33.2% of global cases and 22.7% of US cases were serious, including 1.4% and 1.0% with fatal outcomes, respectively.
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