Suggested remit - To appraise the clinical and cost effectiveness of upadacitinib within its marketing authorisation for previously treated moderate to severe active rheumatoid arthritis
 
Status Proposed
Process STA 2018
ID number 1400

Provisional Schedule

Committee meeting 07 January 2020
Expected publication 18 March 2020

Project Team

Project lead Gemma Barnacle

Email enquiries

Evidence Review Group / Assessment Group Peninsula Technology Assessment Group (PenTAG), University of Exeter

Consultees

Companies sponsors AbbVie (upadacitinib)
Others Department of Health and Social Care
  NHS England
  Welsh Government
Patient carer groups National Rheumatoid Arthritis Society
Professional groups British Society for Rheumatology
  Royal College of Physicians
  Royal College of Radiologists
  UK Clinical Pharmacy Association

Commentators

Assessment group Abbvie (adalimumab) (Confidentiality agreement not signed, not participating)
  Accord Healthcare (methotrexate) (Confidentiality agreement not signed, not participating)
  Amgen (adalimumab)
  Biogen (etanercept, infliximab biosimilar)
  Boehringer Ingelheim International GmbH (adalimumab) (Confidentiality agreement not signed, not participating)
  Bristol-Myers Squibb (abatacept)
  Celltrion (rituximab biosimilar) (Confidentiality agreement not signed, not participating)
  Concordia International (methotrexate) (Confidentiality agreement not signed, not participating)
  Genzyme, a sanofi company (sarilumab)
  hameln pharmaceuticals (methotrexate) (Confidentiality agreement not signed, not participating)
  Hospira (infliximab biosimilar, methotrexate) (Confidentiality agreement not signed, not participating)
  Janssen (golimumab, infliximab)
  Lilly (baricitinib)
  medac GmbH (methotrexate) (Confidentiality agreement not signed, not participating)
  Merck Sharp & Dohme (infliximab biosimilar) (Confidentiality agreement not signed, not participating)
  Napp (rituximab biosimilar, infliximab biosimilar) (Confidentiality agreement not signed, not participating)
  Nordic Pharma (methotrexate) (Confidentiality agreement not signed, not participating)
  Orion Pharma (methotrexate) (Confidentiality agreement not signed, not participating)
  Pfizer (tofacitinib, etanercept, methotrexate)
  Roche Products (tocilizumab, rituximab)
  Rosemont Pharmaceuticals (methotrexate) (Confidentiality agreement not signed, not participating)
  Sandoz (rituximab biosimilar, etanercept, methotrexate) (Confidentiality agreement not signed, not participating)
  Therakind (methotrexate) (Confidentiality agreement not signed, not participating)
  UCB Pharma (certolizumab pegol)
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
  Scottish Medicines Consortium
  Welsh Health Specialised Services Committee

Timeline

Key events during the development of the guidance:

Date Update
01 May 2019 Invitation to participate
24 September 2018 - 22 October 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators

For further information on how we develop guidance, please see our page about NICE technology appraisal guidance