Sylvant

siltuximab · Recordati Netherlands B.V.
AUTHORISED IN THE EU

What Sylvant is used for

Sylvant is indicated for the treatment of adult patients with multicentric Castleman’s disease (MCD who are human immunodeficiency virus (HIV) negative and human herpesvirus-8 (HHV-8) negative.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Sylvant
Active substance
siltuximab
Disease area
Giant Lymph Node Hyperplasia
Medicine group
Immunosuppressants
ATC code
L04AC11
Marketing authorisation holder
Recordati Netherlands B.V.
Authorised in the EU since
2014

Official information

In the USA

Same active substance: Sylvant

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 Sylvant used for?

Sylvant is indicated for the treatment of adult patients with multicentric Castleman’s disease (MCD who are human immunodeficiency virus (HIV) negative and human herpesvirus-8 (HHV-8) negative.

What is the active substance in Sylvant?

Sylvant contains siltuximab.

Who makes Sylvant?

The EU marketing authorisation holder is Recordati Netherlands 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.