🇪🇺 Xospata in European Union

EMA authorised Xospata on 24 October 2019

Marketing authorisation

EMA — authorised 24 October 2019

  • Marketing authorisation holder: ASTELLAS PHARMA EUROPE BV
  • Status: approved

Xospata 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 Xospata approved in European Union?

Yes. EMA authorised it on 24 October 2019.

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

ASTELLAS PHARMA EUROPE BV holds the EU marketing authorisation.