• Hero banner. Pluvicto▼ (lutetium Lu 177 vipivotide tetraxetan). Image of an older man with grey hair. Text: Pluvicto is available for eligible private patients in the United Kingdom.

Pluvicto 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 a PSMA-targeted radioligand therapy (RLT) that delivers DNA-breaking radiation directly to PSMA-positive bone, nodal, and visceral metastases.1–3

Here, you can access relevant information on Pluvicto and a range of engaging resources to solidify your knowledge. Click the links below to explore Pluvicto's mechanism of action, dosing and administration and key efficacy and safety profile data from the VISION trial.

Quick links

Learn more about the mechanism of action of Pluvicto.
Stay up to date with the latest efficacy and safety profile data from the VISION study.
Learn more about the dosing and administration of Pluvicto.

177Lu, lutetium; AR, androgen receptor; DNA, deoxyribonucleic acid; mCRPC, metastatic castration-resistant prostate cancer; PSMA, prostate-specific membrane antigen; RLT, radioligand therapy.

References:

  1. Pluvicto®▼ (lutetium [177Lu] vipivotide tetraxetan) Summary of Product Characteristics.
  2. Benešová M, et al. J Nucl Med 2015;56(6):914–920.
  3. Fendler WP, et al. J Nucl Med 2017;58(11):1786–1792.
UK | February 2025 | FA-11331019
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