Kyprolis

carfilzomib · Amgen Europe B.V.
AUTHORISED IN THE EU

What Kyprolis is used for

Kyprolis in combination with daratumumab and dexamethasone, with lenalidomide and dexamethasone, or with dexamethasone alone is indicated for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Kyprolis
Active substance
carfilzomib
Disease area
Multiple Myeloma
Medicine group
Antineoplastic agents
ATC code
L01XX45
Marketing authorisation holder
Amgen Europe B.V.
Authorised in the EU since
2015

Official information

In the USA

Same active substance: Kyprolis

In India

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 Kyprolis used for?

Kyprolis in combination with daratumumab and dexamethasone, with lenalidomide and dexamethasone, or with dexamethasone alone is indicated for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

What is the active substance in Kyprolis?

Kyprolis contains carfilzomib.

Who makes Kyprolis?

The EU marketing authorisation holder is Amgen Europe 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.

← All specialty medicines, EU

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.