This link will take you to the electronic medicines compendium (emc) website, which is a non-Novartis website.

Image
Hero banner. Pluvicto▼ (lutetium Lu 177 vipivotide tetraxetan) logo.
Image
Hero banner. Pluvicto▼ (lutetium Lu 177 vipivotide tetraxetan) logo.

Pluvicto resources

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.


Resources for 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.

Image
Preview image. Pluvicto patient booklet. Download.

Pluvicto patient booklet

Image
Preview image. Pluvicto patient treatment card. Download.

Pluvicto patient treatment card

To access the PIL for Pluvicto patients in the UK, please visit the electronic medicines compendium (emc) website.



177Lu, lutetium; AR, androgen receptor; mCRPC, metastatic castration-resistant prostate cancer; PIL, patient information leaflet; PSMA, prostate-specific membrane antigen; RLT, radioligand therapy.

Reference

  1. 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.