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Pluvicto®▼ (lutetium [177Lu] vipivotide tetraxetan) is indicated for the treatment of adult patients with prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer (mCRPC) who have been treated with androgen receptor (AR) pathway inhibition and taxane-based chemotherapy or who are not medically suitable for taxanes.1
Pluvicto is available in the United Kingdom to eligible private patients.
To be shared with adult patients in the UK who have been prescribed Pluvicto for their PSMA-positive mCRPC or for whom the prescribing decision has been made.
The resources do not replace the Patient Information Leaflet (PIL) that comes with Pluvicto or advice from the patient’s healthcare team.
177Lu, lutetium; AR, androgen receptor; mCRPC, metastatic castration-resistant prostate cancer; PIL, patient information leaflet; PSMA, prostate-specific membrane antigen; RLT, radioligand therapy.
Reference
Pluvicto®▼ (lutetium [177Lu] vipivotide tetraxetan) Summary of Product Characteristics.
UK | October 2025 | FA-11470230
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.