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EMA Product

Lyxumia

Product approved by European Medicines Agency (EU)

Basic Information

Lyxumia

Regulatory Information

EMEA/H/C/002445

Authorised

January 31, 2013

November 15, 2012

21

September 5, 2024

Company Information

France

82 Avenue Raspail 94250 Gentilly

SANOFI WINTHROP INDUSTRIE

Active Substances Detail

Detailed Information

Therapeutic Indication

### 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.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Lyxumia. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Lyxumia.

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