Suggested remit: To appraise the clinical and cost effectiveness of belantamab mafodotin with pomalidomide and dexamethasone within its marketing authorisation for treating relapsed or refractory multiple myeloma after 1 or more 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:
6211

Project Team

Project lead
Thomas Feist

Email enquiries

If you have any queries please email [email protected]


External Assessment Group:
Liverpool Reviews and Implementation Group, University of Liverpool

Stakeholders

Companies sponsors
GlaxoSmithKline (belantamab mafodotin)
Others
Department of Health and Social Care
 
Health Technology Wales
 
NHS England
Patient carer groups
Blood Cancer UK
 
Myeloma UK
Professional groups
Association of Cancer Physicians
 
Cancer Research UK
 
Royal College of Physicians
 
Royal College of Radiologists
 
UK Myeloma Society
Assessment group
Liverpool Reviews and Implementation Group
Associated public health groups
None
Comparator companies
Amgen (carfilzomib) (confidentiality agreement signed, participating)
 
Janssen-Cilag (bortezomib, daratumumab, teclistamab) (confidentiality agreement signed, participating)
 
Menarini Stemline UK (selinexor) (confidentiality agreement signed, participating)
 
Takeda (confidentiality agreement signed, participating)
 
AbbVie (dexamethasone) (confidentiality agreement not signed, not participating)
 
ADVANZ Pharma (dexamethasone0 (confidentiality agreement not signed, not participating)
 
AS Kalceks (dexamethasone) (confidentiality agreement not signed, not participating)
 
Aspen (dexamethasone) (confidentiality agreement not signed, not participating)
 
Aspire Pharma (bortezomib, dexamethasone) (confidentiality agreement not signed, not participating)
 
Aurobindo Pharma (bortezomib) (confidentiality agreement not signed, not participating)
 
Bausch & Lomb UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
Bristol Myers Squibb Pharmaceuticals (pomalidomide) (confidentiality agreement not signed, not participating)
 
Dr. Reddy's Laboratories UK (bortezomib) (confidentiality agreement not signed, not participating)
 
Glenmark Pharmaceuticals Europe (dexamethasone) (confidentiality agreement not signed, not participating)
 
Hameln pharma (dexamethasone) (confidentiality agreement not signed, not participating)
 
Hospira UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
Krka UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
Martindale Pharma, an Ethypharm Group Company (dexamethasone) (confidentiality agreement not signed, not participating)
 
Medac GmbH (bortezomib) (confidentiality agreement not signed, not participating)
 
MSN Laboratories Europe (bortezomib) (confidentiality agreement not signed, not participating)
 
Mylan (bortezomib) (confidentiality agreement not signed, not participating)
 
Novartis Pharmaceuticals UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
Panpharma UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
ParaPharm Development (dexamethasone) (confidentiality agreement not signed, not participating)
 
Pfizer (bortezomib, elranatamab) (confidentiality agreement not signed, not participating)
 
Pharma & (panobinostat) (confidentiality agreement not signed, not participating)
 
Ranbaxy UK Limited a Sun Pharmaceutical Company (bortezomib) (confidentiality agreement not signed, not participating)
 
Rayner Pharmaceuticals (dexamethasone) (confidentiality agreement not signed, not participating)
 
Rosemont Pharmaceuticals (dexamethasone) (confidentiality agreement not signed, not participating)
 
Sandoz (bortezomib) (confidentiality agreement not signed, not participating)
 
Sanofi (dexamethasone, isatuximab) (confidentiality agreement not signed, not participating)
 
Santen UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
Synchrony Pharma (dexamethasone) (confidentiality agreement not signed, not participating)
 
Teva UK (dexamethasone) (confidentiality agreement not signed, not participating)
 
Thame Laboratories (dexamethasone) (confidentiality agreement not signed, not participating)
 
Thea Pharmaceuticals (dexamethasone) (confidentiality agreement not signed, not participating)
 
Thornton & Ross (bortezomib) (confidentiality agreement not signed, not participating)
 
Tillomed Laboratories (bortezomib) (confidentiality agreement not signed, not participating)
 
Wockhardt UK (dexamethasone) (confidentiality agreement not signed, not participating)
General commentators
All Wales Therapeutics and Toxicology Centre
 
British National Formulary
 
Department of Health - NI
 
Healthcare Improvement Scotland
 
Medicines and Healthcare products Regulatory Agency
 
NHS Wales Joint Commissioning Committee
 
Welsh Government
Relevant research groups
Institute of Cancer Research

Timeline

Key events during the development of the guidance:

Date Update
26 June 2025 - 17 July 2025 Draft guidance
08 January 2025 Committee meeting: 1
08 January 2025 Declaration of interests
05 June 2024 Invitation to participate
15 March 2024 - 16 April 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6211
15 March 2024 In progress. Scoping commencing
09 November 2023 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-June 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.
31 July 2023 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 mid-March 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.
23 November 2022 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