Brexucabtagene autoleucel (original) (raw)

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Brexucabtagene autoleucel, sold under the brand name Tecartus, is a cell-based gene therapy medication for the treatment of mantle cell lymphoma (MCL) and acute lymphoblastic leukemia (ALL). The most common side effects include serious infections, low blood cell counts and a weakened immune system. The most common side effects for the treatment of ALL include fever, CRS, hypotension, encephalopathy, tachycardias, nausea, chills, headache, fatigue, febrile neutropenia, diarrhea, musculoskeletal pain, hypoxia, rash, edema, tremor, infection with pathogen unspecified, constipation, decreased appetite, and vomiting.

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dbo:abstract Brexucabtagene autoleucel, sold under the brand name Tecartus, is a cell-based gene therapy medication for the treatment of mantle cell lymphoma (MCL) and acute lymphoblastic leukemia (ALL). The most common side effects include serious infections, low blood cell counts and a weakened immune system. The most common side effects for the treatment of ALL include fever, CRS, hypotension, encephalopathy, tachycardias, nausea, chills, headache, fatigue, febrile neutropenia, diarrhea, musculoskeletal pain, hypoxia, rash, edema, tremor, infection with pathogen unspecified, constipation, decreased appetite, and vomiting. Brexucabtagene autoleucel is a chimeric antigen receptor T cell therapy and is the first cell-based gene therapy approved by the U.S. Food and Drug Administration (FDA) for the treatment of mantle cell lymphoma. Brexucabtagene autoleucel was approved for medical use in the United States in July 2020, and in the European Union in December 2020. (en)
dbo:alternativeName Tecartus (en)
dbo:drugbank DB15699
dbo:fdaUniiCode 4MD2J2T8SJ
dbo:kegg D11880
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dbo:wikiPageLength 12975 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID 1122713393 (xsd:integer)
dbo:wikiPageWikiLink dbr:Priority_review dbr:Non-Hodgkin's_lymphoma dbr:Cytokine_release_syndrome dbr:Intravenous_therapy dbr:Gene_therapy dbr:Orphan_drug dbr:Boxed_warning dbr:Axicabtagene_ciloleucel dbc:Gilead_Sciences dbr:Acute_lymphoblastic_leukemia dbc:Orphan_drugs dbr:Food_and_Drug_Administration dbr:Breakthrough_therapy dbr:Risk_Evaluation_and_Mitigation_Strategies dbc:Gene_therapy dbc:Breakthrough_therapy dbc:Cancer_treatments dbr:Accelerated_approval_(FDA) dbr:Chimeric_antigen_receptor_T_cell dbr:Mantle_cell_lymphoma dbr:T_cell dbr:B-cell
dbp:atcPrefix None (en)
dbp:dailymedid Brexucabtagene_autoleucel (en)
dbp:drugbank DB15699 (en)
dbp:kegg D11880 (en)
dbp:legalCa Rx-only (en)
dbp:legalEu Rx-only (en)
dbp:legalUs Rx-only (en)
dbp:licenceUs Tecartus (en)
dbp:pregnancyAu C (en)
dbp:pregnancyCategory Not recommended (en)
dbp:routesOfAdministration dbr:Intravenous_therapy
dbp:synonyms KTE-X19 (en)
dbp:tradename Tecartus (en)
dbp:unii 4 (xsd:integer)
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dct:subject dbc:Gilead_Sciences dbc:Orphan_drugs dbc:Gene_therapy dbc:Breakthrough_therapy dbc:Cancer_treatments
rdf:type owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q8386 dbo:Drug
rdfs:comment Brexucabtagene autoleucel, sold under the brand name Tecartus, is a cell-based gene therapy medication for the treatment of mantle cell lymphoma (MCL) and acute lymphoblastic leukemia (ALL). The most common side effects include serious infections, low blood cell counts and a weakened immune system. The most common side effects for the treatment of ALL include fever, CRS, hypotension, encephalopathy, tachycardias, nausea, chills, headache, fatigue, febrile neutropenia, diarrhea, musculoskeletal pain, hypoxia, rash, edema, tremor, infection with pathogen unspecified, constipation, decreased appetite, and vomiting. (en)
rdfs:label Brexucabtagene autoleucel (en)
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is dbo:wikiPageRedirects of dbr:Tecartus
is dbo:wikiPageWikiLink of dbr:List_of_gene_therapies dbr:Intracellular_delivery dbr:Gene_therapy dbr:Lymphoma dbr:Acute_lymphoblastic_leukemia dbr:Mantle_cell_lymphoma dbr:CAR_T_cell dbr:Tecartus
is foaf:primaryTopic of wikipedia-en:Brexucabtagene_autoleucel