EMA — authorised 26 March 2021
- Marketing authorisation holder: ARVELLE THERAPEUTICS NETHERLANDS B.V.
- Status: approved
EMA authorised Xcopri on 26 March 2021
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. EMA authorised it on 26 March 2021.
ARVELLE THERAPEUTICS NETHERLANDS B.V. holds the EU marketing authorisation.