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Novartis FDA approval expands Pluvicto use in earlier prostate cancer

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Sig3.63Sen+4.73Env0.00Soc+2.30Gov+0.43

Radioligand therapies need specialized handling and imaging, so slower-than-expected uptake at centers lacking capacity may limit Pluvicto’s real-world reach despite a broader label. Safety is a watchpoint, with grade 3+ adverse events in just over half of patients in the pivotal trial. Overall survival trends from the PSMAddition trial support earlier treatment intensification discussions as adoption varies by facility capability.

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