For information, the company have advised that they are no longer pursuing a Marketing Authorisation Application from the Medicines and Healthcare products Regulatory Agency (MHRA) for this indication at this time. Therefore, NICE has decided to suspend this appraisal from its current work programme. As this appraisal has been referred NICE will continue to monitor any development and will update interested parties if the situation changes.

Status:
Suspended
Technology type:
Medicine
Decision:
Prioritised
Process:
TA
ID number:
3853

Email enquiries

If you have any queries please email scheduling@nice.org.uk

Timeline

Key events during the development of the guidance:

Date Update
03 June 2025 Suspended. For information, the company have advised that they are no longer pursuing a Marketing Authorisation Application from the Medicines and Healthcare products Regulatory Agency (MHRA) for this indication at this time. Therefore, NICE has decided to suspend this appraisal from its current work programme. As this appraisal has been referred NICE will continue to monitor any development and will update interested parties if the situation changes.
23 January 2025 Note - Note added to the project documents
18 December 2023 Note - Note added to the project documents
17 April 2023 Note - Note added to the project documents
01 December 2022 Note added to the project documents

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