Following a full submission
AWMSG advice |
|||
Status: Recommended with restrictions | |||
Telotristat ethyl (Xermelo®) is recommended as an option for restricted use within NHS Wales. Telotristat ethyl (Xermelo®) is licensed for the treatment of carcinoid syndrome diarrhoea in combination with somatostatin analogue (SSA) therapy in adults inadequately controlled by SSA therapy. Telotristat ethyl (Xermelo®) is restricted for use for the treatment of carcinoid syndrome diarrhoea in adults who are inadequately controlled by SSA therapy and who experience an average of four or more bowel movements a day. Telotristat ethyl (Xermelo®) is not recommended for use within NHS Wales outside of this subpopulation. This recommendation applies only in circumstances where the approved Wales Patient Access Scheme (WPAS) is utilised or where the list/contract price is equivalent or lower than the WPAS price. |
|||
|
|||
Medicine details |
|||
Medicine name | telotristat ethyl (Xermelo®) | ||
Formulation | 250 mg film-coated tablet | ||
Reference number | 2037 | ||
Indication | Treatment of carcinoid syndrome diarrhoea in combination with somatostatin analogue (SSA) therapy in adults inadequately controlled by SSA therapy |
||
Company | Ipsen Ltd | ||
BNF chapter | Malignant disease & immunosuppression | ||
Submission type | Full | ||
Status | Recommended with restrictions | ||
Advice number | 1018 | ||
NMG meeting date | 13/06/2018 | ||
AWMSG meeting date | 18/07/2018 | ||
Date of issue | 23/07/2018 | ||
Date of last review | December 2021 | ||
Commercial arrangement | WPAS |