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lixisenatide (Lyxumia®)

 

Following a full submission

AWMSG advice

Status: Recommended with restrictions

Lixisenatide (Lyxumia®) is recommended as an option for restricted use within NHS Wales. Lixisenatide (Lyxumia®) should be restricted for use in the following circumstances within its licensed indication 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:

  • In combination with basal insulin, with or without oral glucose-lowering medicinal products, in patients uncontrolled on basal insulin;
  • In combination with oral glucose-lowering medicinal products in patients uncontrolled on two or more oral glucose-lowering medicinal products.

Lixisenatide (Lyxumia®) is not recommended for use within NHS Wales outside of these circumstances.

 Final Recommendation: lixisenatide (Lyxumia) 863 (PDF, 219Kb)
 Appraisal Report: lixisenatide (Lyxumia) 863 (PDF, 975Kb)

Medicine details

Medicine name lixisenatide (Lyxumia®)
Formulation 10 micrograms solution for injection and 20 micrograms solution for injection
Reference number 863
Indication

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

Company Sanofi-Aventis Ltd
BNF chapter Endocrine system
Submission type Full
Status Recommended with restrictions
Advice number 3113
NMG meeting date 23/10/2013
AWMSG meeting date 20/11/2013
Ratification by Welsh Government 06/12/2013
Date of issue 13/12/2013
Date of last review 20/01/2017
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