🇪🇺 Lumoxiti in European Union

EMA authorised Lumoxiti on 8 February 2021

Marketing authorisation

EMA — authorised 8 February 2021

  • Marketing authorisation holder: ASTRAZENECA AB
  • Status: approved

Lumoxiti 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 Lumoxiti approved in European Union?

Yes. EMA authorised it on 8 February 2021.

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

ASTRAZENECA AB holds the EU marketing authorisation.