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alogliptin (Vipidia®)

 

Following a full submission

AWMSG advice

Status: Recommended with restrictions

Alogliptin (Vipidia®) is recommended as an option for restricted use for dual oral therapy within NHS Wales. Alogliptin (Vipidia®) should be restricted for use in the following circumstances within its licensed indication for the treatment of adults aged 18 years and older with type 2 diabetes mellitus to improve glycaemic control in combination with other glucose lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control: • In combination with metformin (dual therapy), when metformin alone, together with diet and exercise does not provide adequate glycaemic control in patients for whom the addition of a sulphonylurea is inappropriate; • In combination with a sulphonylurea (dual therapy), when a sulphonylurea alone, together with diet and exercise does not provide adequate glycaemic control in patients for whom the addition of metformin is inappropriate. Alogliptin (Vipidia®) is not recommended for use within NHS Wales outside of these circumstances.

 Final Recommendation: alogliptin (Vipidia) 857 (PDF, 358Kb)
 Appraisal Report: alogliptin (Vipidia) 857 (PDF, 382Kb)

Medicine details

Medicine name alogliptin (Vipidia®)
Formulation 6.25 mg film-coated tablet, 12.5 mg film-coated tablet, 25 mg film-coated tablet
Reference number 857
Indication

In adults aged 18 years and older with type 2 diabetes mellitus to improve glycaemic control in combination with other glucose lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control

Company Takeda UK Ltd
BNF chapter Endocrine system
Submission type Full
Status Recommended with restrictions
Advice number 2914
NMG meeting date 10/09/2014
AWMSG meeting date 08/10/2014
Ratification by Welsh Government 30/10/2014
Date of issue 31/10/2014
Date of last review 13/12/2017
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