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filingDate 2018-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0e2846a3e2ebb9deff876622137fb49
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publicationDate 2019-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber NI-201800136-A
titleOfInvention RADIO-PHARMACEUTICAL COMPLEXES
abstract The invention provides a method for the formation of a thorium complex that targets tissue, said method comprising; a) forming an octadentate chelator comprising four hydroxypyridinone (HOPO) moieties, substituted in the N position with a methyl group, and a coupling moiety ending in a carboxylic acid group; b) coupling said octadentate chelator to at least one tissue-targeting moiety that targets prolyl endopeptidase FAP; and c) contacting said tissue-targeting chelating agent with an aqueous solution comprising an ion of at least one alpha-emitting thorium isotope. A method is provided for the treatment of a neoplastic or hyperplastic disease comprising the administration of a thorium complex that targets such tissue, as well as the corresponding complex and pharmaceutical formulations.
priorityDate 2016-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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