Lutetium (177Lu) vipivotide tetraxetan (original) (raw)

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dbo:abstract Lutetium(177Lu)vipivotidtetraxetan (177Lu-PSMA-617) ist ein Arzneistoff aus der Gruppe der Radiotherapeutika. Unter dem Namen Pluvicto (Hersteller: Novartis) wurde er im März 2022 in den USA zugelassen zur Behandlung einer bestimmten Form von Prostatakrebs. (de) Lutetium (177Lu) vipivotide tetraxetan, sold under the brand name Pluvicto, is a radiopharmaceutical medication used for the treatment of prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC). Lutetium (177Lu) vipivotide tetraxetan is a targeted radioligand therapy. The most common adverse reactions include fatigue, dry mouth, nausea, anemia, decreased appetite, and constipation. Lutetium (177Lu) vipivotide tetraxetan is a radioconjugate composed of PSMA-617, a human prostate-specific membrane antigen (PSMA)-targeting ligand, conjugated to the beta-emitting radioisotope lutetium-177, with potential antineoplastic activity against PSMA-expressing tumor cells. Upon intravenous administration of lutetium (177Lu) vipivotide tetraxetan, vipivotide tetraxetan targets and binds to PSMA-expressing tumor cells. Upon binding, PSMA-expressing tumor cells are destroyed by 177Lu through the specific delivery of beta particle radiation. PSMA, a tumor-associated antigen and type II transmembrane protein, is expressed on the membrane of prostatic epithelial cells and overexpressed on prostate tumor cells. Lutetium (177Lu) vipivotide tetraxetan was approved for medical use in the United States in March 2022. In October 2022, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency recommended the approval of Pluvicto to treat prostate cancer in the European Union. (en)
dbo:alternativeName Pluvicto (en)
dbo:casNumber 1703749-62-5
dbo:class dbr:Radiopharmaceutical
dbo:drugbank DB16778
dbo:fdaUniiCode G6UF363ECX
dbo:kegg D12335
dbo:pubchem 122706785
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dbp:atcPrefix None (en)
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dbp:class dbr:Radiopharmaceutical
dbp:dailymedid Pluvicto (en)
dbp:drugName Lutetium vipivotide tetraxetan (en)
dbp:drugbank DB16778 (en)
dbp:kegg D12335 (en)
dbp:legalCa Rx-only (en)
dbp:legalUs Rx-only (en)
dbp:pubchem 122706785 (xsd:integer)
dbp:routesOfAdministration dbr:Intravenous
dbp:smiles [177Lu+3].OCCC[C@H]CO (en)
dbp:stdinchi 1 (xsd:integer)
dbp:stdinchikey RSTDSVVLNYFDHY-BGOLSCJMSA-K (en)
dbp:synonyms 177 (xsd:integer)
dbp:tradename Pluvicto (en)
dbp:unii G6UF363ECX (en)
dbp:usan Lutetium Lu 177 vipivotide tetraxetan (en)
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rdfs:comment Lutetium(177Lu)vipivotidtetraxetan (177Lu-PSMA-617) ist ein Arzneistoff aus der Gruppe der Radiotherapeutika. Unter dem Namen Pluvicto (Hersteller: Novartis) wurde er im März 2022 in den USA zugelassen zur Behandlung einer bestimmten Form von Prostatakrebs. (de) Lutetium (177Lu) vipivotide tetraxetan, sold under the brand name Pluvicto, is a radiopharmaceutical medication used for the treatment of prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC). Lutetium (177Lu) vipivotide tetraxetan is a targeted radioligand therapy. The most common adverse reactions include fatigue, dry mouth, nausea, anemia, decreased appetite, and constipation. Lutetium (177Lu) vipivotide tetraxetan was approved for medical use in the United States in March 2022. (en)
rdfs:label Lutetium(177Lu)vipivotidtetraxetan (de) Lutetium (177Lu) vipivotide tetraxetan (en)
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foaf:name Lutetium (177Lu) vipivotide tetraxetan (en)
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