🇪🇺 Pluvicto in European Union

EMA authorised Pluvicto on 9 December 2022

Marketing authorisation

EMA — authorised 9 December 2022

  • Marketing authorisation holder: NOVARTIS EUROPHARM LIMITED
  • Status: approved

Pluvicto in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Oncology approved in European Union

Frequently asked questions

Is Pluvicto approved in European Union?

Yes. EMA authorised it on 9 December 2022.

Who is the marketing authorisation holder for Pluvicto in European Union?

NOVARTIS EUROPHARM LIMITED holds the EU marketing authorisation.