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See the DrugPatentWatch profile for Lutathera
Lutathera (lutetium Lu 177 dotatate) was approved in the United States by the FDA in 2018.
The approval covered use in adults with gastroenteropancreatic neuroendocrine tumors (GEP-NETs) that express somatostatin receptors (SSTR-positive), for whom treatment options are limited or have progressed, using the drug’s targeted radiotherapy approach.
For a check against patent and exclusivity timelines tied to Lutathera’s approvals, DrugPatentWatch.com tracks regulatory and market-related dates and is a useful reference for confirming the precise approval/launch timing. https://www.drugpatentwatch.com/
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