Suggested remit: To appraise the clinical and cost effectiveness of Deutetrabenazine within its marketing authorisation for treating tardive dyskinesia.

Status:
In progress
Technology type:
Medicine
Decision:
Selected
Reason for decision:
Anticipate the topic will be of importance to patients, carers, professionals, commissioners and the health of the public to ensure clinical benefit is realised, inequalities in use addressed, and help them make the best use of NHS resources
Further information:
Scoping commenced.
Process:
STA Standard
ID number:
6550

Project Team

Project lead
Emily Richards

Email enquiries

If you have any queries please email [email protected]

Timeline

Key events during the development of the guidance:

Date Update
22 May 2025 - 20 June 2025 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6550
22 May 2025 In progress. Scoping commenced.
04 March 2025 Topic selection

For further information on our processes and methods, please see our CHTE processes and methods manual