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Basel, 28 March 2025: Novartis announced today that the US Food and Drug Administration (FDA) approved Pluvicto® (lutetium Lu 177 vipivotide tetraxetan) for patients with prostate-specific membrane antigen (PSMA)-positive metastatic castr......
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Source : Novartis
Novartis
US Food and Drug Administration
androgen receptor pathway inhibitor (ARPI) therapy
approved Pluvicto® (lutetium Lu 177 vipivotide tetraxetan)
prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC)
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