Suggested remit: To appraise the clinical and cost effectiveness of encorafenib with cetuximab and folinic acid, fluorouracil and oxaliplatin (FOLFOX) within its marketing authorisation for treating adults with untreated BRAF V600E mutation-positive metastatic colorectal cancer.

Status:
In progress
Technology type:
Medicine
Decision:
Selected
Decision publication date:
04 February 2026
Prioritisation programme:
Medicines evaluation
Rationale:

Criteria within the (VPAG) met as a significant licence extension. 

Process:
STA Standard
ID number:
6734

Project Team

Project lead
scopingta@nice.org.uk

Email enquiries

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

Timeline

Key events during the development of the guidance:

Date Update
05 August 2026 - 02 September 2026 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6734
05 August 2026 In progress. Scoping commencing
04 February 2026 Awaiting development. Status change linked to topic prioritisation decision being set to Selected
04 February 2026 Topic prioritisation

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