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Published in 2023 at "Drugs of today"
DOI: 10.1358/dot.2023.59.1.3476574
Abstract: On March 23, 2022, the U.S. Food and Drug Administration (FDA) approved Pluvicto (lutetium Lu 177 vipivotide tetraxetan), also known as 177Lu-PSMA-617, for the treatment of adult patients with metastatic castration-resistant prostate cancer (mCRPC) who…
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Keywords:
177 vipivotide;
prostate;
lutetium 177;
vipivotide tetraxetan ... See more keywords