Sacubitril

drug
On this page

Also known as AHU-377AHU377Sacubitril component of entrestoSacubitriloSACUBITRIL HEMICALCIUM SALTShakubattam

Summary

Sacubitril (CHEMBL3137301) is an approved small molecule; indicated across 13 conditions including congestive heart failure and heart failure.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • Indications: 13 conditions
  • Clinical trials: 72
  • Chemistry: 411.5 Da · C24H29NO5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3137301
NameSacubitril
TypeSmall molecule
Max phase4
FDA approvedno
PubChem CID9811834
Molecular formulaC24H29NO5
Molecular weight411.5
InChIKeyPYNXFZCZUAOOQC-UTKZUKDTSA-N

SMILES: CCOC(=O)[C@H](C)C[C@@H](CC1=CC=C(C=C1)C2=CC=CC=C2)NC(=O)CCC(=O)O

IUPAC name: 4-[[(2S,4R)-5-ethoxy-4-methyl-5-oxo-1-(4-phenylphenyl)pentan-2-yl]amino]-4-oxobutanoic acid

Also known as: AHU-377, AHU377, Sacubitril, Sacubitril component of entresto, Sacubitrilo, SACUBITRIL, SACUBITRIL HEMICALCIUM SALT, sacubitril, Sacubitril hemicalcium salt, Shakubattam

Patent coverage: 578 distinct patent families (1,401 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

13 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
congestive heart failure4MONDO:0005009EFO:0000373
heart failure4MONDO:0005252EFO:0003144
hypertensive disorder3MONDO:0005044EFO:0000537
myocardial infarction3MONDO:0005068EFO:0000612
Chagas cardiomyopathy3MONDO:0005491EFO:0005529
acute myocardial infarction3MONDO:0004781EFO:0008583
ST-elevation myocardial infarction3MONDO:0041656EFO:0008585
pulmonary hypertension3MONDO:0005149MONDO:0005149
hypertrophic cardiomyopathy2MONDO:0005045EFO:0000538
peripheral arterial disease2MONDO:0005386EFO:0004265
aortic valve insufficiency2MONDO:0005648EFO:0007148
essential hypertension2MONDO:0001134MONDO:0001134
severe acute respiratory syndrome1MONDO:0005091MONDO:0100096

Clinical trials

Total trials: 72.

Phase distribution

PhaseTrials
PHASE424
Not specified22
PHASE312
PHASE27
PHASE13
PHASE2/PHASE32
PHASE1/PHASE22

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06218199PHASE4RECRUITINGDiuretics vs. Afterload Reduction for Treatment of HeartLogic Alerts
NCT06501651PHASE4NOT_YET_RECRUITINGSacubitril/Valsartan Treats Patients With Essential Hypertension and Type 2 Diabetic Nephropathy
NCT06704633PHASE4NOT_YET_RECRUITINGSacubitril-valsartan in Patients With Heart Failure With Reduced Ejection Fraction From Rural Tanzania
NCT06917664PHASE4RECRUITINGTreatment of Moderate Ischemic Mitral Regurgitation in Patients With Coronary Artery Disease
NCT07241338PHASE4NOT_YET_RECRUITINGSacubitril/Allisartan for Hypertensive Patients With Overweight or Obesity
NCT07572032PHASE4NOT_YET_RECRUITINGDelayed Initiation of ARNI and SGLT2i in Heart Failure With Corrected Aetiology (DELAY-HF), Pilot Study
NCT02554890PHASE4COMPLETEDComparison of Sacubitril/Valsartan Versus Enalapril on Effect on NT-proBNP in Patients Stabilized From an Acute Heart Failure Episode.
NCT02787798PHASE4TERMINATEDEvaluation of the Entresto Effect on Sympathic Nervous System in Patient With Heart Failure
NCT02788656PHASE4TERMINATEDPulmonary Artery Pressure Reduction With ENTresto (Sacubitril/Valsartan)
NCT02970669PHASE4COMPLETEDStudy on the Effects of Sacubitril/Valsartan on Physical Activity and Sleep in Heart Failure With Reduced Ejection Fraction Patients.
NCT03119623PHASE4WITHDRAWNComparing ARNI With ACE Inhibitor on Endothelial Function
NCT03300427PHASE4COMPLETEDThe Effects of Sacubitril/Valsartan on Cardiac Oxygen Consumption and Efficiency of Cardiac Work in Heart Failure Patients
NCT03553303PHASE4UNKNOWNPharmacodynamic Effects of Sacubitril/Valsartan on Natriuretic Peptides, Angiotensin and Neprilysin
NCT04023227PHASE4COMPLETEDEfficacy and Safety of Sacubitril/Valsartan Compared With Enalapril on Morbidity, Mortality, and NT-proBNP Change in Patients With CCC
NCT04197050PHASE4UNKNOWNEffect of Sacubitril/Valsartan on Reduced Right Ventricular Ejection Fraction in Patients With CTD
NCT04342351PHASE4UNKNOWNEarly Treatment of ARNI on Myocardial Remodeling and Progress
NCT04572724PHASE4UNKNOWNThe Effect of Sacubitril/Valsartan on Cardiovascular Events in Dialysis Patients and Efficacy Prediction of Baseline LVEF Value
NCT04929600PHASE4UNKNOWNSacubitril/Valsartan Versus Amlodipine in Hypertension and Left Ventricular Hypertrophy.
NCT05060588PHASE4UNKNOWNSacubitril/Valsartan Versus Valsartan for Hypertensive Patients With Acute Myocardial Infarction
NCT05243199PHASE4COMPLETEDSacubitril/Valsartan for CKD5 Stage Dialysis Patients
NCT05387967PHASE4COMPLETEDSafety and Tolerability of Sacubitril/Valsartan in Heart Failure Patient With Reduced Ejection Fraction
NCT05881720PHASE4COMPLETEDSacubitril/Valsartan Versus Valsartan in Heart Failure
NCT06035978PHASE4UNKNOWNDetermination of Drug Levels for Pharmacotherapy of Heart Failure
NCT07417215PHASE4COMPLETEDThe Effect of Sacubitril and Valsartan on Heart Function in Chronic Hemodialysis Patients With HFpEF
NCT05508035PHASE3RECRUITINGThe Effect of Sacubitril/valsartan Versus Ramipril on Left Ventricular Function and Remodeling in Patients with Ischemic Heart Failure with Mid-range Ejection Fraction
NCT06712030PHASE3NOT_YET_RECRUITINGEffect of Angiotensin Receptor/Neprilysin Inhibitors on Transthyretin Cardiac Amyloidosis and Heart Failure with Reduced Ejection Fraction
NCT06716970PHASE3NOT_YET_RECRUITINGQR12000 Compound Tablets in Patients with Moderate to Severe Essential Hypertension
NCT03066804PHASE3COMPLETEDA Randomized, Double-blind Controlled Study Comparing LCZ696 to Medical Therapy for Comorbidities in HFpEF Patients
NCT03552575PHASE3COMPLETEDThe Effects of Sacubitril/Valsartan Compared to Valsartan on LV Remodelling in Asymptomatic LV Systolic Dysfunction After MI
NCT03785405PHASE3COMPLETEDOpen-label Extension Study to Evaluate Long-term Safety of Sacubitril/Valsartan in Pediatric Patients With HF
NCT03988634PHASE3COMPLETEDChanges in NT-proBNP, Safety, and Tolerability in HFpEF Patients With a WHF Event (HFpEF Decompensation) Who Have Been Stabilized and Initiated at the Time of or Within 30 Days Post-decompensation (PARAGLIDE-HF)
NCT04637555PHASE3WITHDRAWNOpen-label Extension Study for CLCZ696G2301 (PARADISE-MI)
NCT04753112PHASE3COMPLETEDTreatment of PH With Angiotensin II Receptor Blocker and Neprilysin Inhibitor in HFpEF Patients With CardioMEMS Device
NCT04853758PHASE3UNKNOWNAngiotensin Receptor-Neprilysin Inhibition in Chagas Cardiomyopathy With Reduced Ejection Fraction: ANSWER-HF.
NCT05366101PHASE2/PHASE3COMPLETEDLifestyle and Pharmacological Interventions in Hypertrophic Cardiomyopathy
NCT05545059PHASE3UNKNOWNEffects and Safety of Sacubitril/Valsartan on Refractory Hypertension
NCT06149104PHASE3COMPLETEDA Safety Study of Sacubitril/Valsartan in Japanese Pediatric Patients With Heart Failure Due to Systemic Left Ventricle Systolic Dysfunction Who Have Completed CLCZ696B2319E1 Study
NCT07023016PHASE2/PHASE3COMPLETEDComparative Assessment of Efficacy & Safety of Sacubitril/Valsartan Versus Ramipril in Patients With Renal Dysfunction Hospitalized With Acute Decompensated Heart Failure
NCT05279742PHASE1/PHASE2ENROLLING_BY_INVITATIONEnhancing the Natriuretic Peptide System in HFpEF
NCT00549770PHASE2COMPLETEDEfficacy and Safety of LCZ696A in Patients With Essential Hypertension

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).