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Drug ReportsLutetium dotatate lu-177
Lutetium dotatate lu-177
EndolucinBeta, Lumark (lutetium dotatate lu-177) is an unknown pharmaceutical. Lutetium dotatate lu-177 was first approved as Lumark on 2015-06-18. It has been approved in Europe to treat radionuclide imaging.
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diagnosisD003933
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91 clinical trials
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Indications Phases 4
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Ontology
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Neuroendocrine tumorsD018358EFO_1001901D3A.81725711154
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Carcinoid tumorD002276—D3A.00—32——5
Gastro-enteropancreatic neuroendocrine tumorC535650——112——3
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Neuroendocrine carcinomaD018278——16———6
Pancreatic neoplasmsD010190EFO_0003860C2534——16
ParagangliomaD010235——14———4
MeningiomaD008579EFO_0003098D32.914———4
PheochromocytomaD010673——13———3
NeoplasmsD009369—C80—2——13
Merkel cell carcinomaD015266EFO_1001471C4A12———2
NeuroblastomaD009447EFO_0000621—11———2
Breast neoplasmsD001943EFO_0003869C50—1———1
Pituitary neoplasmsD010911———1———1
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Indications Phases 1
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ThymomaD013945——1————1
MesotheliomaD008654—C451————1
GlioblastomaD005909EFO_0000515—1————1
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Thyroid neoplasmsD013964EFO_0003841—————11
HyperthyroidismD006980—E05.9————11
Stomach neoplasmsD013274EFO_0003897C16————11
Gastrointestinal neoplasmsD005770—C26.9————11
Digestive system neoplasmsD004067——————11
Gastrointestinal diseasesD005767——————11
Germ cell and embryonal neoplasmsD009373——————11
Endocrine system diseasesD004700EFO_0001379E34.9————11
Neoplasms by histologic typeD009370——————11
Intestinal neoplasmsD007414—C26.0————11
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameLutetium dotatate lu-177
INN—
Description
Lutetium (177Lu) oxodotreotide (INN) or 177Lu DOTA-TATE, trade name Lutathera, is a chelated complex of a radioisotope of the element lutetium with DOTA-TATE, used in peptide receptor radionuclide therapy (PRRT). Specifically, it is used in the treatment of cancers which express somatostatin receptors.
Classification
Small molecule
Drug classAntineoplastic agent
Image (chem structure or protein)Loading
Structure (InChI/SMILES or Protein Sequence)—
Identifiers
PDB—
CAS-ID—
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ChEMBL IDCHEMBL3989924
ChEBI ID—
PubChem CID—
DrugBankDB13985
UNII ID—
Target
No data
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No data
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PubMed Central
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1,292 adverse events reported
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