Suggested remit: To appraise the clinical and cost effectiveness of iptacopan within its marketing authorisation for treating complement 3 (C3) glomerulopathy.
 
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 6283

Provisional Schedule

Committee meeting 13 August 2025
Expected publication 08 January 2026

Project Team

Project lead Kate Moore

Email enquiries

External Assessment Group Kleijnen Systematic Reviews Ltd

Stakeholders

Companies sponsors Novartis (iptacopan)
Others Department of Health and Social Care
  NHS England
Patient carer groups Kidney Care UK
  Kidney Research UK
  MPGN/DDD Support Group
  National Kidney Federation
Professional groups Royal College of Pathologists
  UK Kidney Association
Comparator companies Alexion Pharma (eculizumab)
  Amgen (eculizumab) - not participating
  Roche (mycophenolate mofetil) - not participating
  Rosemont Pharmaceuticals (mycophenolate mofetil) - not participating
  Samsung Bioepis (eculizumab) - not participating
  Teva Pharma (mycophenolate mofetil) - not participating
  Tillomed Laboratories (mycophenolate mofetil) - not participating
Evidence review group National Institute for Health Research Health Technology Assessment Programme (NETSCC)
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

Timeline

Key events during the development of the guidance:

Date Update
14 January 2025 Invitation to participate
07 October 2024 - 04 November 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6283
07 October 2024 In progress. Scoping commencing
28 April 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