Suggested remit: To appraise the clinical and cost effectiveness of tralokinumab within its marketing authorisation for treating moderate to severe atopic dermatitis.

Status:
Discontinued
Decision:
Prioritised
Process:
TA
ID number:
3734

Project Team

Project lead
Shonagh D'Sylva

Email enquiries

If you have any queries please email TAteam2@nice.org.uk


External Assessment Group:
BMJ Technology Assessment Group (BMJ-TAG), BMJ

Stakeholders

Companies sponsors
Leo Pharma (tralokinumab)
Others
Department of Health and Social Care
 
NHS England
 
Welsh Government
Patient carer groups
National Eczema Society
Professional groups
British Association of Dermatologists
 
Royal College of Physicians
Associated public health groups
None
Comparator companies
GlaxoSmithKline (alitretion)
 
Novartis Pharmaceuticals (ciclosporin, mycophenolate mofetil)
 
Pfizer (methotrexate)
 
Sanofi (dupilumab)
General commentators
All Wales Therapeutics and Toxicology Centre
 
British National Formulary
 
Department of Health, Social Services and Public Safety for Northern Ireland
 
Healthcare Improvement Scotland
 
Medicines and Healthcare products Regulatory Agency
 
Scottish Medicines Consortium
 
Welsh Health Specialised Services Committee
Relevant research groups
None

Timeline

Key events during the development of the guidance:

Date Update
05 August 2021 Note added to the project documents
05 August 2021 Discontinued
04 August 2021 Schedule affected by COVID-19. We are continuing to face significant capacity challenges and will be delaying the development of tralokinumab for treating moderate to severe atopic dermatitis [ID3734]. This topic will now be considered as part of a multiple technology appraisal [ID3960]. We anticipate that it will be considered by the technology appraisal committee in March 2022.
09 February 2021 Invitation to participate
05 October 2020 Note added to the project documents
05 October 2020 In progress. Topic is in progress
22 July 2020 - 19 August 2020 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators

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