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