Lyxumia

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Withdrawn

This medicine's authorisation has been withdrawn

lixisenatide
MedicineHumanWithdrawn

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 18 December 2025, the European Commission withdrew the marketing authorisation for Lyxumia (lixisenatide) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Sanofi Winthrop Industrie, which notified the European Commission of its decision to permanently discontinue the marketing of the product for commercial reasons.

Lyxumia was granted marketing authorisation in the EU on 1 February 2013 for treatment of type 2 diabetes. The marketing authorisation was initially valid for a 5-year period. It was then granted unlimited validity on 18 September 2017.

Lyxumia is GLP-1 receptor agonist. There are therapeutic alternatives such as other GLP-1 receptor agonists authorised and available throughout the EU for the treatment of type 2 diabetes.

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Product information

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Latest procedure affecting product information:N/0000223999
27/08/2024
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This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

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Product details

Name of medicine
Lyxumia
Active substance
lixisenatide
International non-proprietary name (INN) or common name
lixisenatide
Therapeutic area (MeSH)
Diabetes Mellitus, Type 2
Anatomical therapeutic chemical (ATC) code
A10BJ03

Pharmacotherapeutic group

  • Drugs used in diabetes
  • Glucagon-like peptide-1 (GLP-1) analogues

Therapeutic indication

Lyxumia is indicated for the treatment of adults with type 2 diabetes mellitus to achieve glycaemic control in combination with oral glucose lowering medicinal products and/or basal insulin when these, together with diet and exercise, do not provide adequate glycaemic control.

Authorisation details

EMA product number
EMEA/H/C/002445
Marketing authorisation holder
Sanofi Winthrop Industrie

82 Avenue Raspail
94250 Gentilly
FRANCE

Opinion adopted
15/11/2012
Marketing authorisation issued
31/01/2013
Withdrawal of marketing authorisation
18/12/2025
Revision
21

Assessment history

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