bempedoic acid 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
5382 738606-46-7

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • bempedoic acid
  • ETC-1002
  • ESP-55016
  • nexletol
  • nilemdo
Bempedoic acid is an adenosine triphosphate-citrate lyase (ACL) inhibitor that lowers low-density lipoprotein cholesterol (LDL-C) by inhibition of cholesterol synthesis in the liver. ACL is an enzyme upstream of 3-hydroxy-3-methyl-glutaryl-coenzyme A (HMG-CoA) reductase in the cholesterol biosynthesis pathway. Bempedoic acid and its active metabolite, ESP15228, require coenzyme A (CoA) activation by very long-chain acyl-CoA synthetase 1 (ACSVL1) to ETC-1002-CoA and ESP15228-CoA, respectively. ACSVL1 is expressed primarily in the liver. Inhibition of ACL by ETC-1002-CoA results in decreased cholesterol synthesis in the liver and lowers LDL-C in blood via upregulation of low-density lipoprotein receptors
  • Molecular weight: 344.49
  • Formula: C19H36O5
  • CLOGP: 3.95
  • LIPINSKI: 0
  • HAC: 5
  • HDO: 3
  • TPSA: 94.83
  • ALOGS: -4.21
  • ROTB: 14

  • Status: ONP

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

DoseUnitRoute
0.18 g O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 2 Bocci G, Oprea TI, Benet LZ

Approvals:

DateAgencyCompanyOrphan
April 1, 2020 EMA FGK Representative Service GmbH
Feb. 21, 2020 FDA ESPERION THERAPS INC

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Myalgia 209.74 52.58 69 501 146460 63341992

FDA Adverse Event Reporting System (Male)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Myalgia 129.96 85.71 41 247 84069 34872574

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Myalgia 235.35 56.45 78 575 185563 79558172
Blood creatine phosphokinase increased 60.41 56.45 22 631 66068 79677667

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC C10AX15 CARDIOVASCULAR SYSTEM
LIPID MODIFYING AGENTS
LIPID MODIFYING AGENTS, PLAIN
Other lipid modifying agents
ATC C10BA10 CARDIOVASCULAR SYSTEM
LIPID MODIFYING AGENTS
LIPID MODIFYING AGENTS, COMBINATIONS
Combinations of various lipid modifying agents
MeSH PA D000963 Antimetabolites
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D007004 Hypoglycemic Agents
MeSH PA D000960 Hypolipidemic Agents
MeSH PA D057847 Lipid Regulating Agents
FDA EPC N0000193913 Adenosine Triphosphate-Citrate Lyase Inhibitor
FDA MoA N0000193914 Adenosine Triphosphate-Citrate Lyase Inhibitors
CHEBI has role CHEBI:35679 antilipemic drugs
CHEBI has role CHEBI:50266 Prodrugs
CHEBI has role CHEBI:149598 EC 2.3.3.8 (ATP citrate synthase) inhibitors

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Atherosclerotic occlusive disease indication 129573006
Familial hypercholesterolemia - heterozygous indication 238079002




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 4.87 acidic
pKa2 5.47 acidic

Orange Book patent data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRoutePatent numberPatent expiration datePatent use
180MG NEXLETOL ESPERION THERAPS INC N211616 Feb. 21, 2020 RX TABLET ORAL 10118881 Dec. 23, 2023 USE OF NEXLETOL AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG NEXLETOL ESPERION THERAPS INC N211616 Feb. 21, 2020 RX TABLET ORAL 10941095 Dec. 23, 2023 USE OF NEXLETOL AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG NEXLETOL ESPERION THERAPS INC N211616 Feb. 21, 2020 RX TABLET ORAL 8497301 Dec. 23, 2023 USE OF NEXLETOL AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG NEXLETOL ESPERION THERAPS INC N211616 Feb. 21, 2020 RX TABLET ORAL 9000041 Dec. 23, 2023 USE OF NEXLETOL AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG NEXLETOL ESPERION THERAPS INC N211616 Feb. 21, 2020 RX TABLET ORAL 9624152 Dec. 23, 2023 USE OF NEXLETOL AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY FOR INHIBITING CHOLESTEROL SYNTHESIS TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL 10118881 Dec. 23, 2023 USE OF NEXLIZET AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL 10941095 Dec. 23, 2023 USE OF NEXLIZET AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL 8497301 Dec. 23, 2023 USE OF NEXLIZET AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL 9000041 Dec. 23, 2023 USE OF NEXLIZET AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL 9624152 Dec. 23, 2023 USE OF NEXLIZET AS AN ADJUNCT TO DIET AND MAXIMALLY TOLERATED STATIN THERAPY FOR INHIBITING CHOLESTEROL SYNTHESIS TO LOWER LDL-C IN ADULTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL 10912751 March 14, 2036 A METHOD OF TREATING HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE BY DECREASING THE LEVEL OF LDL-C USING A FIXED DOSE COMBINATION OF 180 MG BEMPEDOIC ACID AND 10 MG EZETIMIBE

Orange Book exclusivity data (new drug applications)

Formulation strengthTrade nameApplicantApplication numberApproval dateTypeDose formRouteExclusivity dateDescription
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL Feb. 26, 2023 NEW PRODUCT
180MG NEXLETOL ESPERION THERAPS INC N211616 Feb. 21, 2020 RX TABLET ORAL Feb. 21, 2025 NEW CHEMICAL ENTITY
180MG;10MG NEXLIZET ESPERION THERAPS INC N211617 Feb. 26, 2020 RX TABLET ORAL Feb. 21, 2025 NEW CHEMICAL ENTITY

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
ATP-citrate synthase Enzyme INHIBITOR Ki 5.69 SCIENTIFIC LITERATURE DRUG LABEL

External reference:

IDSource
1EJ6Z6Q368 UNII
C3659310 UMLSCUI
CHEBI:149601 CHEBI
CHEMBL3545313 ChEMBL_ID
10472693 PUBCHEM_CID
DB11936 DRUGBANK_ID
9891 INN_ID
C581236 MESH_SUPPLEMENTAL_RECORD_UI
D10691 KEGG_DRUG
8321 IUPHAR_LIGAND_ID
018287 NDDF
870523005 SNOMEDCT_US
870609002 SNOMEDCT_US
4039212 VANDF
2282403 RXNORM
331395 MMSL
38188 MMSL
d09518 MMSL

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Nexletol HUMAN PRESCRIPTION DRUG LABEL 1 72426-118 TABLET, FILM COATED 180 mg ORAL NDA 31 sections
Nexletol HUMAN PRESCRIPTION DRUG LABEL 1 72426-118 TABLET, FILM COATED 180 mg ORAL NDA 31 sections
Nexletol HUMAN PRESCRIPTION DRUG LABEL 1 72426-118 TABLET, FILM COATED 180 mg ORAL NDA 31 sections
Nexlizet HUMAN PRESCRIPTION DRUG LABEL 2 72426-818 TABLET, FILM COATED 180 mg ORAL NDA 31 sections
Nexlizet HUMAN PRESCRIPTION DRUG LABEL 2 72426-818 TABLET, FILM COATED 180 mg ORAL NDA 31 sections
Nexlizet HUMAN PRESCRIPTION DRUG LABEL 2 72426-818 TABLET, FILM COATED 180 mg ORAL NDA 31 sections