🇪🇺 KCP-330 in European Union

EMA authorised KCP-330 on 26 March 2021

Marketing authorisation

EMA — authorised 26 March 2021

  • Application: EMEA/H/C/005127
  • Marketing authorisation holder: Stemline Therapeutics B.V.
  • Local brand name: Nexpovio
  • Indication: NEXPOVIO is indicated in combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-CD38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.
  • Status: approved

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Frequently asked questions

Is KCP-330 approved in European Union?

Yes. EMA authorised it on 26 March 2021.

Who is the marketing authorisation holder for KCP-330 in European Union?

Stemline Therapeutics B.V. holds the EU marketing authorisation.