Suggested remit - To appraise the clinical and cost effectiveness of lenadogene nolparvovec within its marketing authorisation for treating Leber's hereditary optic neuropathy

Please note that following on from information received from the company, NICE has decided to suspend this evaluation from its current work programme. The timelines for this evaluation are to be aligned with the latest regulatory and UK launch expectations and further information regarding the scheduling of this evaluation will be available in due course.

Status:
Suspended
Technology type:
Medicine
Decision:
Prioritised
Process:
TA
ID number:
1410

Project Team

Project lead
Daniel Davies

Email enquiries

If you have any queries please email TATeam3@nice.org.uk

Timeline

Key events during the development of the guidance:

Date Update
13 June 2023 Suspended. Please note that following on from information received from the company, NICE has decided to suspend this evaluation from its current work programme. The timelines for this evaluation are to be aligned with the latest regulatory and UK launch expectations and further information regarding the scheduling of this evaluation will be available in due course.
07 February 2023 Invitation to participate
07 November 2022 - 07 December 2022 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
05 July 2022 Note added to the project documents
11 May 2022 Note added to the project documents
21 June 2021 - 02 July 2021 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
21 June 2021 Note added to the project documents
01 September 2020 In progress. Topic is in progress
01 September 2020 Note added to the project documents
25 September 2018 - 23 October 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators

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