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Lutathera ® : The First FDA- and EMA-Approved Radiopharmaceutical for Peptide Receptor Radionuclide...

Lutathera ® : The First FDA- and EMA-Approved Radiopharmaceutical for Peptide Receptor Radionuclide...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1a0bd205f21540e7b1cbd5c910755766

Lutathera ® : The First FDA- and EMA-Approved Radiopharmaceutical for Peptide Receptor Radionuclide Therapy

About this item

Full title

Lutathera ® : The First FDA- and EMA-Approved Radiopharmaceutical for Peptide Receptor Radionuclide Therapy

Author / Creator

Publisher

Switzerland: MDPI AG

Journal title

Pharmaceuticals (Basel, Switzerland), 2019-07, Vol.12 (3), p.114

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

As the first radiopharmaceutical for Peptide Receptor Radionuclide Therapy (PRRT), Lutathera
was approved by the EMA in 2017 and the FDA in 2018 for the treatment of somatostatin receptor (SSTR) positive gastroenteropancreatic neuroendocrine tumors. Using the concept of PRRT, Lutathera
combines the radionuclide
Lu with the somatostatin ana...

Alternative Titles

Full title

Lutathera ® : The First FDA- and EMA-Approved Radiopharmaceutical for Peptide Receptor Radionuclide Therapy

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_1a0bd205f21540e7b1cbd5c910755766

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1a0bd205f21540e7b1cbd5c910755766

Other Identifiers

ISSN

1424-8247

E-ISSN

1424-8247

DOI

10.3390/ph12030114

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