Stem definition | Drug id | CAS RN |
---|---|---|
5382 | 738606-46-7 |
Dose | Unit | Route |
---|---|---|
0.18 | g | O |
Property | Value | Reference |
---|---|---|
BDDCS (Biopharmaceutical Drug Disposition Classification System) | 2 | Bocci G, Oprea TI, Benet LZ |
Date | Agency | Company | Orphan |
---|---|---|---|
April 1, 2020 | EMA | FGK Representative Service GmbH | |
Feb. 21, 2020 | FDA | ESPERION THERAPS INC |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Myalgia | 209.74 | 52.58 | 69 | 501 | 146460 | 63341992 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Myalgia | 129.96 | 85.71 | 41 | 247 | 84069 | 34872574 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients 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 |
None
Source | Code | Description |
---|---|---|
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 |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Atherosclerotic occlusive disease | indication | 129573006 | |
Familial hypercholesterolemia - heterozygous | indication | 238079002 |
None
None
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 4.87 | acidic |
pKa2 | 5.47 | acidic |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent 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 |
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
---|---|---|---|---|---|---|---|---|---|
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 |
Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
---|---|---|---|---|---|---|---|---|---|
ATP-citrate synthase | Enzyme | INHIBITOR | Ki | 5.69 | SCIENTIFIC LITERATURE | DRUG LABEL |
ID | Source |
---|---|
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 |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
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 |