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:
6269

Provisional Schedule

Committee meeting:
11 November 2025
Expected publication:
29 January 2026

Project Team

Project lead
Leena Issa

Email enquiries

If you have any queries please email [email protected]

Stakeholders

Companies sponsors
Eli Lilly
Others
Department of Health and Social Care
 
NHS England
Patient carer groups
Blood Cancer UK
 
CLL Support
 
Leukaemia UK
 
Lymphoma Action
Professional groups
Association of Cancer Physicians
 
British Oncology Pharmacy Association
 
Cancer Research UK
 
Royal College of Physicians
 
Royal College of Radiologists
Associated public health groups
None
Comparator companies
Abbvie (venetoclax) – confidentiality agreement signed, participating
 
AstraZeneca (acalabrutinib) – confidentiality agreement signed, participating
 
BeOne Medicines UK (zanubrutinib) – confidentiality agreement signed, participating
 
Celltrion Healthcare (rituximab) – confidentiality agreement not signed, not participating
 
Gilead Sciences (idelalisib) – confidentiality agreement not signed, not participating
 
Janssen-Cilag (ibrutinib) – confidentiality agreement signed, participating
 
Pfizer (rituximab) – confidentiality agreement not signed, not participating
 
Roche (rituximab) – confidentiality agreement not signed, not participating
 
Sandoz (rituximab) – confidentiality agreement not signed, not participating
General commentators
All Wales Therapeutics and Toxicology Centre
 
British National Formulary
 
Department of Health – Northern Ireland
 
Healthcare Improvement Scotland
 
Medicines and Healthcare products Regulatory Agency
 
NHS Wales Joint Commissioning Committee
 
Scottish Medicines Consortium
 
Welsh Government
Relevant research groups
Institute of Cancer Research

Timeline

Key events during the development of the guidance:

Date Update
11 April 2025 Invitation to participate
21 February 2025 - 07 March 2025 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
08 August 2024 Please note that following on from advice received from the company this appraisal has been rescheduled to align with latest regulatory expectations. Therefore, we now anticipate that the appraisal will begin during mid-April 2025 when we will write to you about how you can get involved. The deadline for submissions is expected in approximately late June 2025.
04 April 2024 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 late October 2024. 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.
28 February 2024 - 27 March 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6269
28 February 2024 In progress. Scoping commenced.
20 March 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