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

Stem definitionDrug idCAS RN
5332 None

Description:

MoleculeDescription

Synonyms:

  • onasemnogene abeparvovec
  • onasemnogene abeparvovec-xioi
  • zolgensma
  • AVXS-101
ZOLGENSMA is a recombinant AAV9-based gene therapy designed to deliver a copy of the gene encoding the human SMN protein. SMA is caused by a bi-allelic mutation in the SMN1 gene, which results in insufficient SMN protein expression. Intravenous administration of ZOLGENSMA that results in cell transduction and expression of the SMN protein has been observed in two human case studies
  • Molecular weight:
  • Formula:
  • CLOGP:
  • LIPINSKI: None
  • HAC: None
  • HDO: None
  • TPSA:
  • ALOGS:
  • ROTB: None

Drug dosage:

None

ADMET properties:

None

Approvals:

DateAgencyCompanyOrphan
May 18, 2020 EMA Novartis Europharm Limited
May 24, 2019 FDA NOVARTIS PHARMS CORP

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
Aspartate aminotransferase increased 296.92 50.12 112 2043 90165 63396702
Alanine aminotransferase increased 253.98 50.12 104 2051 103666 63383201
Troponin I increased 180.01 50.12 35 2120 2203 63484664
Pyrexia 168.15 50.12 133 2022 470345 63016522
Thrombocytopenia 148.98 50.12 81 2074 151076 63335791
Transaminases increased 125.00 50.12 45 2110 31322 63455545
Vomiting 97.03 50.12 106 2049 559511 62927356
Thrombotic microangiopathy 81.62 50.12 25 2130 10536 63476331
Platelet count decreased 71.38 50.12 46 2109 116076 63370791
Troponin T increased 67.23 50.12 14 2141 1240 63485627
Blood lactate dehydrogenase increased 62.46 50.12 25 2130 23091 63463776
Hepatic enzyme increased 56.56 50.12 50 2105 202278 63284589

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
Aspartate aminotransferase increased 235.50 47.88 95 1511 67688 34887637
Alanine aminotransferase increased 193.32 47.88 87 1519 80728 34874597
Troponin I increased 191.93 47.88 40 1566 2642 34952683
Pyrexia 133.38 47.88 114 1492 332899 34622426
Hepatic enzyme increased 115.52 47.88 49 1557 39031 34916294
Transaminases increased 87.10 47.88 36 1570 26787 34928538
Thrombocytopenia 75.46 47.88 60 1546 156187 34799138
Vomiting 75.29 47.88 73 1533 247548 34707777
Liver function test increased 66.37 47.88 25 1581 14540 34940785
Rhinovirus infection 54.59 47.88 16 1590 4283 34951042
Platelet count decreased 49.30 47.88 42 1564 119675 34835650
Blood lactate dehydrogenase increased 49.07 47.88 23 1583 22967 34932358

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
Aspartate aminotransferase increased 442.64 46.39 176 3015 138465 79602732
Alanine aminotransferase increased 365.93 46.39 161 3030 162409 79578788
Pyrexia 213.04 46.39 191 3000 678518 79062679
Troponin I increased 207.13 46.39 46 3145 4692 79736505
Thrombocytopenia 198.47 46.39 126 3065 265133 79476064
Transaminases increased 182.80 46.39 71 3120 51672 79689525
Hepatic enzyme increased 124.46 46.39 82 3109 182528 79558669
Vomiting 114.25 46.39 136 3055 665692 79075505
Platelet count decreased 107.96 46.39 77 3114 194587 79546610
Blood lactate dehydrogenase increased 107.94 46.39 45 3146 39125 79702072
Thrombotic microangiopathy 83.05 46.39 31 3160 20138 79721059
Liver function test increased 62.78 46.39 31 3160 39742 79701455
Rhinovirus infection 59.07 46.39 19 3172 7934 79733263
Troponin increased 52.58 46.39 22 3169 19233 79721964
Troponin T increased 50.55 46.39 14 3177 3508 79737689
Increased bronchial secretion 46.72 46.39 13 3178 3314 79737883

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC M09AX09 MUSCULO-SKELETAL SYSTEM
OTHER DRUGS FOR DISORDERS OF THE MUSCULO-SKELETAL SYSTEM
OTHER DRUGS FOR DISORDERS OF THE MUSCULO-SKELETAL SYSTEM
Other drugs for disorders of the musculo-skeletal system

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

DiseaseRelationSNOMED_IDDOID
Spinal muscular atrophy indication 5262007 DOID:12377




🐶 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:

None

External reference:

IDSource
MLU3LU3EVV UNII
C5140028 UMLSCUI
CHEMBL4297240 ChEMBL_ID
DB15528 DRUGBANK_ID
D11559 KEGG_DRUG
10619 INN_ID
C000710948 MESH_SUPPLEMENTAL_RECORD_UI
018004 NDDF
788110002 SNOMEDCT_US
789426004 SNOMEDCT_US
1922968-73-7 SECONDARY_CAS_RN
2170225 RXNORM
36975 MMSL
36979 MMSL
d09287 MMSL

Pharmaceutical products:

None