Suggested remit: To appraise the clinical and cost effectiveness tovorafenib within its marketing authori-sation treating people aged 6 months and over with relapsed or refractory paediatric low-grade glioma (LGG) with a BRAF fusion or rearrangement or BRAF V600 mutation.

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
Process:
STA Standard
ID number:
6557

Provisional Schedule

Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6557:
11 July 2025 - 08 August 2025

Project Team

Project lead
Emily Richards

Email enquiries

If you have any queries please email [email protected]

Related links

Timeline

Key events during the development of the guidance:

Date Update
11 July 2025 In progress. Scoping commencing
07 February 2025 Awaiting development. Status change linked to Topic Selection Decision being set to Selected

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