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

Stem definitionDrug idCAS RN
human origin 5179 1174395-19-7

Description:

MoleculeDescription

Synonyms:

  • kyntheum
  • brodalumab
  • AMG 827
  • AMG-827
Brodalumab is a human monoclonal IgG2 antibody that selectively binds to human IL-17RA and inhibits its interactions with cytokines IL-17A, IL-17F, IL-17C, IL-17A/F heterodimer and IL-25. IL-17RA is a protein expressed on the cell surface and is a required component of receptor complexes utilized by multiple IL-17 family cytokines. Blocking IL­17RA inhibits IL-17 cytokine-induced responses including the release of pro-inflammatory cytokines and chemokines.
  • Molecular weight:
  • Formula:
  • CLOGP:
  • LIPINSKI: None
  • HAC: None
  • HDO: None
  • TPSA:
  • ALOGS:
  • ROTB: None

Drug dosage:

DoseUnitRoute
15 mg P

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
July 17, 2017 EMA LEO Pharma A/S
Feb. 15, 2017 FDA VALEANT LUXEMBOURG
July 4, 2016 PMDA

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
Psoriatic arthropathy 62.90 47.34 21 413 47011 50557679
Collagen-vascular disease 48.21 47.34 6 428 78 50604612

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
Psoriatic arthropathy 75.08 42.72 24 779 14667 29559057
Dermatitis infected 64.01 42.72 9 794 91 29573633
Tinea pedis 54.17 42.72 11 792 1082 29572642
Peripheral venous disease 45.89 42.72 11 792 2317 29571407
Therapy interrupted 44.01 42.72 14 789 8372 29565352

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
Psoriatic arthropathy 88.64 34.41 33 1248 43248 64454203
Dermatitis infected 59.83 34.41 9 1272 208 64497243
Tinea pedis 56.27 34.41 12 1269 2049 64495402
Psoriasis 45.41 34.41 24 1257 71679 64425772
Collagen-vascular disease 43.98 34.41 6 1275 67 64497384
Drug ineffective 39.61 34.41 64 1217 840183 63657268
Peripheral venous disease 38.35 34.41 11 1270 6327 64491124
Therapy interrupted 36.32 34.41 14 1267 20022 64477429
Suicidal ideation 35.80 34.41 20 1261 66522 64430929
Parakeratosis 34.50 34.41 6 1275 349 64497102

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC L04AC12 ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
IMMUNOSUPPRESSANTS
IMMUNOSUPPRESSANTS
Interleukin inhibitors
FDA CS M0001357 Antibodies, Monoclonal
MeSH PA D003879 Dermatologic Agents
FDA EPC N0000193276 Interleukin-17 Receptor A Antagonist
FDA MoA N0000193279 Interleukin 17 Receptor A Antagonists

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

DiseaseRelationSNOMED_IDDOID
Plaque psoriasis indication 200965009
Non-radiographic axial spondyloarthritis indication 713777005
Crohn's disease contraindication 34000006




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

None

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Interleukin-17 receptor Membrane receptor ANTIBODY BINDING Kd 9.20 IUPHAR SCIENTIFIC LITERATURE

External reference:

IDSource
6ZA31Y954Z UNII
4036541 VANDF
C3491331 UMLSCUI
CHEMBL1742996 ChEMBL_ID
D10061 KEGG_DRUG
DB11776 DRUGBANK_ID
9475 INN_ID
7540 IUPHAR_LIGAND_ID
1872251 RXNORM
32390 MMSL
d08529 MMSL
726519005 SNOMEDCT_US
763604008 SNOMEDCT_US
017103 NDDF
C571216 MESH_SUPPLEMENTAL_RECORD_UI

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
Siliq HUMAN PRESCRIPTION DRUG LABEL 1 0187-0004 INJECTION 210 mg SUBCUTANEOUS BLA 27 sections