EMA — authorised 17 June 2021
- Marketing authorisation holder: Regeneron Ireland Designated Activity Company (DAC)
- Status: approved
🇪🇺 Evkeeza in European Union
EMA authorised Evkeeza on 17 June 2021
Marketing authorisation
Evkeeza in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Other Metabolic approved in European Union
Frequently asked questions
Is Evkeeza approved in European Union?
Yes. EMA authorised it on 17 June 2021.
Who is the marketing authorisation holder for Evkeeza in European Union?
Regeneron Ireland Designated Activity Company (DAC) holds the EU marketing authorisation.