dbo:abstract |
Inebilizumab, sold under the brand name Uplizna, is a medication for the treatment of neuromyelitis optica spectrum disorder (NMOSD) in adults. The most common adverse reactions include urinary tract infection, headache, joint pain (arthralgia), nausea and back pain. Inebilizumab is a humanized mAb that binds to and depletes CD19+ B cells including plasmablasts and plasma cells. The U.S. Food and Drug Administration (FDA) considers it to be a first-in-class medication. (en) イネビリズマブ(Inebilizumab)は、成人の視神経脊髄炎スペクトラム障害(NMOSD)を治療する為の医薬品である。形質細胞やプラズマ細胞を含むCD19+ B細胞に結合し、これを除去するヒト化モノクローナル抗体である。 主な副作用は、尿路感染症、頭痛、関節痛(人工関節痛)、吐き気、腰痛などである。 米国食品医薬品局(FDA)は、本薬を画期的医薬品と位置付けている。 (ja) |
dbo:alternativeName |
Uplizna (en) |
dbo:casNumber |
1299440-37-1 |
dbo:class |
dbr:Antineoplastic_agent |
dbo:drugbank |
DB12530 |
dbo:fdaUniiCode |
74T7185BMM |
dbo:kegg |
D11757 |
dbo:wikiPageExternalLink |
https://druginfo.nlm.nih.gov/drugportal/name/inebilizumab |
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50977311 (xsd:integer) |
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12736 (xsd:nonNegativeInteger) |
dbo:wikiPageRevisionID |
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dbo:wikiPageWikiLink |
dbr:International_nonproprietary_name dbr:MedImmune dbr:Orphan_drug dbr:Committee_for_Medicinal_Products_for_Human_Use dbc:Orphan_drugs dbr:European_Medicines_Agency dbr:Food_and_Drug_Administration dbc:Antineoplastic_drugs dbc:Monoclonal_antibodies dbr:Thomas_Tedder dbr:CD19 dbr:Neuromyelitis_optica dbr:United_States_Adopted_Name dbr:First-in-class_medication dbr:Intravenous dbr:Antineoplastic_agent |
dbp:atcPrefix |
L04 (en) |
dbp:atcSuffix |
AA47 (en) |
dbp:c |
6504 (xsd:integer) |
dbp:casNumber |
1299440 (xsd:integer) |
dbp:chemspiderid |
None (en) |
dbp:class |
dbr:Antineoplastic_agent |
dbp:dailymedid |
Inebilizumab (en) |
dbp:drugbank |
DB12530 (en) |
dbp:h |
10080 (xsd:integer) |
dbp:kegg |
D11757 (en) |
dbp:legalUs |
Rx-only (en) |
dbp:mabType |
mab (en) |
dbp:n |
1732 (xsd:integer) |
dbp:o |
2044 (xsd:integer) |
dbp:routesOfAdministration |
dbr:Intravenous |
dbp:s |
44 (xsd:integer) |
dbp:source |
zu (en) |
dbp:synonyms |
MEDI-551, inebilizumab-cdon (en) |
dbp:target |
dbr:CD19 |
dbp:tradename |
Uplizna (en) |
dbp:type |
mab (en) |
dbp:unii |
74 (xsd:integer) |
dbp:wikiPageUsesTemplate |
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dcterms:subject |
dbc:Orphan_drugs dbc:Antineoplastic_drugs dbc:Monoclonal_antibodies |
rdf:type |
owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q8386 dbo:MonoclonalAntibody dbo:Drug |
rdfs:comment |
Inebilizumab, sold under the brand name Uplizna, is a medication for the treatment of neuromyelitis optica spectrum disorder (NMOSD) in adults. The most common adverse reactions include urinary tract infection, headache, joint pain (arthralgia), nausea and back pain. Inebilizumab is a humanized mAb that binds to and depletes CD19+ B cells including plasmablasts and plasma cells. The U.S. Food and Drug Administration (FDA) considers it to be a first-in-class medication. (en) イネビリズマブ(Inebilizumab)は、成人の視神経脊髄炎スペクトラム障害(NMOSD)を治療する為の医薬品である。形質細胞やプラズマ細胞を含むCD19+ B細胞に結合し、これを除去するヒト化モノクローナル抗体である。 主な副作用は、尿路感染症、頭痛、関節痛(人工関節痛)、吐き気、腰痛などである。 米国食品医薬品局(FDA)は、本薬を画期的医薬品と位置付けている。 (ja) |
rdfs:label |
Inebilizumab (en) イネビリズマブ (ja) |
owl:sameAs |
yago-res:Inebilizumab wikidata:Inebilizumab dbpedia-ja:Inebilizumab https://global.dbpedia.org/id/2P8YK |
prov:wasDerivedFrom |
wikipedia-en:Inebilizumab?oldid=1123986817&ns=0 |
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wikipedia-en:Inebilizumab |
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dbr:Uplizna |
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is dbp:medication of |
dbr:Neuromyelitis_optica_spectrum_disorder |
is foaf:primaryTopic of |
wikipedia-en:Inebilizumab |