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lixisenatide (Lyxumia®)


Reference No. 863

Publication date:
13/12/2013


Last review date:
20/01/2017

Appraisal information

lixisenatide (Lyxumia®) 10 micrograms solution for injection
lixisenatide (Lyxumia®) 20 micrograms solution for injection


Company: Sanofi-Aventis Ltd
BNF category: Endocrine system
NMG meeting date: 23/10/2013
AWMSG meeting date: 20/11/2013
   
   
Submission Type: Full Submission
Status: Recommended with restrictions
Advice No: 3113
Ministerial ratification: 06/12/2013

Current Progress


Submission
received
NMG
meeting
AWMSG
meeting
Ministerial
Ratification

AWMSG advice

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 Appraisal Recommendation (FAR)
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AWMSG Secretariat Appraisal Report (ASAR)
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Clinical Expert (CE) Summary
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