Status In progress
Technology type Medicine
Decision Selected
Process STA Standard
ID number 1136

Project Team

Project lead Jeremy Powell

Email enquiries

Stakeholders

Companies sponsors Bristol-Myers Squibb
Others Department of Health
  NHS England
Patient carer groups Bowel Cancer UK
Professional groups Association of Cancer Physicians
  Cancer Research UK
  Royal College of Physicians
  Royal College of Radiologists
Comparator companies Amgen (panitumumab) CAU not signed (not participating)
  Dr Reddy’s Laboratories (capecitabine) CAU not signed (not participating)
  Glenmark Pharmaceuticals (capecitabine) CAU not signed (not participating)
  Medac (folinic acid, fluorouracil, irinotecan, oxaliplatin) CAU not signed (not participating)
  Merck (cetuximab) CAU not signed (not participating)
  MSD (pembrolizumab) CAU signed - participating
  Pfizer (irinotecan) CAU not signed (not participating)
  Ranbaxy (irinotecan, oxaliplatin) CAU not signed (not participating)
  Seacross Pharmaceuticals (irinotecan, oxaliplatin) CAU not signed (not participating)
General commentators All Wales Therapeutics and Toxicology Centre
  Allied Health Professionals Federation
  British National Formulary
  Department of Health - Northern Ireland
  Healthcare Improvement Scotland
  Medicines and Healthcare products Regulatory Agency
  Scottish Medicines Consortium
  Welsh Government
  Welsh Health Specialised Services Committee
Relevant research groups Institute of Cancer Research

Timeline

Key events during the development of the guidance:

Date Update
26 April 2024 In progress. Consultees have been invited to make submissions.
26 April 2024 Invitation to participate
30 November 2023 Please note that following on from advice received from the company this appraisal has been rescheduled. We now anticipate that the appraisal will begin during late-April 2024 when we will write to you about how you can get involved. The deadline for submissions is expected in approximately late-June 2024.
03 August 2023 Awaiting development. Please note that following on from information received from the company, this appraisal has now been scheduled back into the work programme. The timelines for this appraisal have been revised and the appraisal is now anticipated to begin during mid-March 2024 when we will write to you about how you can get involved.
31 January 2018 Suspended. The company have notified the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) that it wishes to withdraw its application for a marketing authorisation for nivolumab for this indication. The NICE appraisal of nivolumab for previously treated metastatic colorectal cancer with high microsatellite instability or mismatch repair deficiency [ID1136] will therefore be suspended.
16 November 2017 Committee meeting: 1
26 June 2017 In progress. Appraisal has started
23 June 2017 Invitation to participate
23 March 2017 - 13 April 2017 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators
02 March 2017 Referral

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