Suggested remit: To appraise the clinical and cost effectiveness of durvalumab within its marketing authorisation for treating resectable gastric and gastro-oesophageal junction cancer.

Status:
In progress
Technology type:
Medicine
Decision:
Awaiting decision
Process:
STA Standard
ID number:
6374

Project Team

Project lead
Jeremy Powell

Email enquiries

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

Timeline

Key events during the development of the guidance:

Date Update
03 September 2025 Invitation to participate
16 July 2025 - 13 August 2025 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
16 July 2025 In progress. Scoping commenced.
20 January 2025 Note - Note added to the project documents
23 December 2024 Awaiting development. Please note that following on from a request received from the company, the timelines for this appraisal have been revised and the appraisal is now anticipated to begin in early July 2025. These timings are based on a request from the company to reschedule the initial date set by NICE, in order to facilitate a suitably comprehensive and robust submission.
21 June 2024 Note - Note added to the project documents
25 October 2023 Topic selection

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