Suggested remit: To appraise the clinical and cost effectiveness of spesolimab within its marketing authorisation for treating generalised pustular psoriasis flares in adults.
 
Status In progress
Technology type Medicine
Decision Selected
Process STA Standard
ID number 3963

Provisional Schedule

Committee meeting: 1 08 January 2025
Expected publication 19 March 2025

Project Team

Project lead Jeremy Powell

Email enquiries

External Assessment Group Southampton Health Technology Assessment Centre (SHTAC), University of Southampton

Stakeholders

Companies sponsors Boehringer Ingelheim Ltd (spesolimab)
Others Department of Health and Social Care
  NHS England
Patient carer groups Changing Faces
  Gene People
  Genetic Alliance UK
  Psoriasis and Psoriatic Arthritis Alliance
  Psoriasis Association
  Psoriasis Help Organisation
  South Asian Health Foundation
  Specialised Healthcare Alliance
Professional groups Association of Genetic Nurses & Counsellors
  British Association of Dermatologists
  British Dermatological Nursing Group
  British Geriatrics Society
  British Society for Cutaneous Allergy
  British Society for Genetic Medicine
  Primary Care Dermatology Society
  Royal College of General Practitioners
  Royal College of Nursing
  Royal College of Pathologists
  Royal College of Physicians
  Royal Pharmaceutical Society
  Royal Society of Medicine
  St John’s Institute of Dermatology
  UK Clinical Pharmacy Association
Associated public health groups Public Health Wales
  UK Health Security Agency
Comparator companies AbbVie (adalimumab, risankizumab)
  Accord Healthcare (methotrexate)
  Advanz Pharma (methotrexate)
  Almirall (dimethyl fumarate, tildrakizumab)
  Amgen (adalimumab, apremilast)
  Aspire Pharma (dimethyl fumarate)
  Biogen Idec (adalimumab, dimethyl fumarate, etanercept, infliximab)
  Bristol Myers Squibb (deucravacitinib)
  B&S Colorama (ciclosporin)
  Celltrion Healthcare UK (adalimumab, infliximab)
  Celix Pharma (dimethyl fumarate)
  Dexcel-Pharma (ciclosporin)
  Eli Lilly and Company (ixekizumab)
  Fresenius Kabi (adalimumab)
  Genus Pharmaceuticals (acitretin, dimethyl fumarate)
  Hospira UK (methotrexate)
  Johnson & Johnson Innovative Medicine (guselkumab, ustekinumab)
  Leo Pharma (brodalumab)
  Medac GmbH (methotrexate)
  Merck Sharp & Dohme (infliximab)
  Morningside Healthcare (acitretin, ciclosporin, methotrexate)
  Mylan (ciclosporin, dimethyl fumarate)
  Nordic Pharma (methotrexate)
  Novartis Pharmaceuticals UK (ciclosporin, secukinumab)
  Orion Pharma (UK) (methotrexate)
  Pfizer (etanercept, infliximab, methotrexate)
  Rosemont Pharmaceuticals (methotrexate)
  Sandoz (adalimumab, etanercept, infliximab, methotrexate)
  Santen UK (ciclosporin)
  Teva UK (acitretin, ciclosporin, methotrexate)
  Therakind Limited (methotrexate)
  UCB Pharma (bimekizumab, certolizumab pegol)
  Viatris (ciclosporin)
  Wockhardt (dimethyl fumarate)
  Zentiva (dimethyl fumarate)
General commentators All Wales Therapeutics and Toxicology Centre
  Allied Health Professionals Federation
  Board of Community Health Councils in Wales
  British National Formulary
  Care Quality Commission
  Department of Health - Northern Ireland
  Healthcare Improvement Scotland
  Medicines and Healthcare products Regulatory Agency
  National Association of Primary Care
  National Pharmacy Association
  NHS Confederation
  Scottish Medicines Consortium
  Welsh Government
  Welsh Health Specialised Services Committee
Relevant research groups British Skin Foundation
  Centre of Evidence-based Dermatology, University of Nottingham
  Cochrane Skin Group
  Dermatrust
  Genomics England
  MRC Clinical Trials Unit
  National Institute for Health Research

Timeline

Key events during the development of the guidance:

Date Update
19 June 2024 Invitation to participate
16 March 2023 We had previously said that this appraisal was expected to start in approximately early-February 2023. The company have asked NICE to delay the appraisal. The appraisal will therefore be rescheduled and an update on the revised timelines will be provided when further information is available.
26 October 2022 (10:00) Scoping workshop
07 September 2022 - 05 October 2022 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
07 September 2022 In progress. Scoping commencing

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