🇪🇺 Alecensa in European Union

EMA authorised Alecensa on 16 February 2017

Marketing authorisation

EMA — authorised 16 February 2017

  • Marketing authorisation holder: Roche Registration Limited
  • Status: approved

Alecensa 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 Alecensa approved in European Union?

Yes. EMA authorised it on 16 February 2017.

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

Roche Registration Limited holds the EU marketing authorisation.