MedPath

Sacubitril

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

Overview

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

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/06/15
Phase 2
Completed
National Heart Institute, Egypt
2025/04/10
Phase 1
Completed
Humanis Saglık Anonim Sirketi
2024/12/02
Phase 3
Not yet recruiting
Puerta de Hierro University Hospital
2024/11/26
Phase 4
Not yet recruiting
Martin Rohacek
2024/04/10
Phase 4
Completed
Pachankis, Yang I., M.D.
2024/02/22
Phase 1
Not yet recruiting
2024/02/20
Phase 1
Not yet recruiting
2024/02/08
Phase 1
Not yet recruiting
2024/01/05
Phase 1
Not yet recruiting
Dr. Reddy's Laboratories (Thailand) Limited
2023/11/29
N/A
Recruiting
University Hospital, Grenoble

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Novartis Pharmaceuticals Corporation
0078-0777
ORAL
49 mg in 1 1
2/18/2022
Aphena Pharma Solutions - Tennessee, LLC
71610-806
ORAL
49 mg in 1 1
3/28/2024
Aphena Pharma Solutions - Tennessee, LLC
71610-810
ORAL
24 mg in 1 1
4/2/2024
Novartis Pharmaceuticals Corporation
0078-9659
ORAL
24 mg in 1 1
2/18/2022
Novartis Pharmaceuticals Corporation
0078-0696
ORAL
97 mg in 1 1
2/18/2022
Novartis Pharmaceuticals Corporation
0078-0659
ORAL
24 mg in 1 1
2/18/2022
Novartis Pharmaceuticals Corporation
0078-9777
ORAL
49 mg in 1 1
2/18/2022

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
MERAVO FILM-COATED TABLETS 200MG
SIN16874P
TABLET, FILM COATED
97mg
9/28/2023
MERAVO FILM-COATED TABLETS 50MG
SIN16872P
TABLET, FILM COATED
24mg
9/28/2023
MERAVO FILM-COATED TABLETS 100MG
SIN16873P
TABLET, FILM COATED
49mg
9/28/2023

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

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