Suggested remit: To appraise the clinical and cost effectiveness of pembrolizumab with chemotherapy with or without bevacizumab, within its marketing authorisation for treating platinum-resistant recurrent ovarian cancer after 1 or 2 treatments.

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:
6363

Project Team

Project lead
Jennifer Upton

Email enquiries

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

Timeline

Key events during the development of the guidance:

Date Update
01 December 2025 Invitation to participate
19 September 2025 - 17 October 2025 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6363
05 July 2024 Note - Note added to the project documents
09 February 2024 In progress. In progress
22 September 2023 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