Bavencio

avelumab · Merck Europe B.V.
AUTHORISED IN THE EU

What Bavencio is used for

Bavencio is indicated as monotherapy for the treatment of adult patients with metastatic Merkel cell carcinoma (MCC). Bavencio in combination with axitinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma (RCC). Bavencio is indicated as monotherapy for the first-line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are progression-free following platinum-based chemotherapy.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Bavencio
Active substance
avelumab
Disease area
Neuroendocrine Tumors
Medicine group
Other antineoplastic agents;Monoclonal antibodies
ATC code
L01FF04
Marketing authorisation holder
Merck Europe B.V.
Authorised in the EU since
2017

Official information

In the USA

Same active substance: Bavencio

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 Bavencio used for?

Bavencio is indicated as monotherapy for the treatment of adult patients with metastatic Merkel cell carcinoma (MCC). Bavencio in combination with axitinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma (RCC). Bavencio is indicated as monotherapy for the first-line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are progression-free following platinum-based chemotherapy.

What is the active substance in Bavencio?

Bavencio contains avelumab.

Who makes Bavencio?

The EU marketing authorisation holder is Merck 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.

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