🇪🇺 Brukinsa in European Union

EMA authorised Brukinsa on 22 November 2021

Marketing authorisation

EMA — authorised 22 November 2021

  • Marketing authorisation holder: BEIGENE IRELAND LTD
  • Status: approved

Brukinsa 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 Brukinsa approved in European Union?

Yes. EMA authorised it on 22 November 2021.

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

BEIGENE IRELAND LTD holds the EU marketing authorisation.