Following a full submission
AWMSG advice |
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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. |
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Medicine details |
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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 |
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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 |