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telotristat ethyl (Xermelo®)

 

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.

 Final Recommendation: telotristat ethyl (Xermelo) 2037 (PDF, 341Kb)
 Appraisal Report: telotristat ethyl (Xermelo) 2037 (PDF, 352Kb)

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
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