Nexpovio

selinexor · Stemline Therapeutics B.V.
AUTHORISED IN THE EU

What Nexpovio is used for

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.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Nexpovio
Active substance
selinexor
Disease area
Multiple Myeloma
Medicine group
Antineoplastic agents
ATC code
L01XX66
Marketing authorisation holder
Stemline Therapeutics B.V.
Authorised in the EU since
2021

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Nexpovio used for?

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.

What is the active substance in Nexpovio?

Nexpovio contains selinexor.

Who makes Nexpovio?

The EU marketing authorisation holder is Stemline Therapeutics B.V..

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

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