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
Further information Selected
Process STA Standard
ID number 6293

Provisional Schedule

Committee meeting 04 September 2024
Expected publication 13 November 2024

Project Team

Project lead Kate Moore

Email enquiries

External Assessment Group Liverpool Reviews and Implementation Group, University of Liverpool

Stakeholders

Companies sponsors Eli Lilly (selpercatinib)
Others Department of Health and Social Care
  NHS England
Professional groups Association of Cancer Physicians
  British Thoracic Oncology Group
  Cancer Research UK
  Royal College of Physicians
  Royal College of Radiologists
Assessment group Institute of Cancer Research
Comparator companies Accord Healthcare (cisplatin, carboplatin, docetaxel, gemcitabine, paclitaxel, vinorelbine) – confidentiality agreement not signed, not participating
  Boehringer Ingelheim (nintedanib) – confidentiality agreement not signed, not participating
  Bristol-Myers Squibb (nivolumab) – confidentiality agreement not signed, not participating
  Celgene (paclitaxel, nab-paclitaxel) – confidentiality agreement not signed, not participating
  Consilient Health Ltd (carboplatin, vinorelbine) – confidentiality agreement not signed, not participating
  Dr Reddy’s Laboratories (docetaxel, pemetrexed) – confidentiality agreement not signed, not participating
  Fresenius Kabi (docetaxel, paclitaxel) – confidentiality agreement not signed, not participating
  Fresenius Kabi Oncology (carboplatin, gemcitabine) – confidentiality agreement not signed, not participating
  Hospira UK (cisplatin, carboplatin, docetaxel, gemcitabine, paclitaxel) – confidentiality agreement not signed, not participating
  Medac GmbH (vinorelbine) – confidentiality agreement not signed, not participating
  Merck Sharp & Dohme (pembrolizumab)
  Pfizer (carboplatin, cisplatin, docetaxel, gemcitabine, paclitaxel) – confidentiality agreement not signed, not participating
  Pierre Fabre Ltd (vinorelbine) – confidentiality agreement not signed, not participating
  Roche Products (atezolizumab, bevacizumab, erlotinib) – confidentiality agreement not signed, not participating
  Sandoz Ltd (cisplatin) – confidentiality agreement not signed, not participating
  Sanofi (docetaxel) – confidentiality agreement not signed, not participating
  Seacross Pharmaceuticals (docetaxel, paclitaxel) – confidentiality agreement not signed, not participating
  Sun Pharma (carboplatin, gemcitabine) – confidentiality agreement not signed, not participating
  Teva UK (carboplatin, cisplatin, docetaxel, paclitaxel) – confidentiality agreement not signed, not participating
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 Government
  Welsh Health Specialised Services Committee

Timeline

Key events during the development of the guidance:

Date Update
05 February 2024 Invitation to participate
08 December 2023 - 19 January 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
11 December 2023 In progress

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