Suggested remit: To appraise the clinical and cost effectiveness of pembrolizumab with pemetrexed and platinum-based chemotherapy within its marketing authorisation for untreated unresectable advanced malignant pleural mesothelioma.
For information, the company have advised that the wording of the marketing authorisation for pembrolizumab with pemetrexed and platinum-based chemotherapy for untreated unresectable advanced malignant pleural mesothelioma is still to be determined and therefore they have requested a temporary suspension of this appraisal while this issue is resolved. NICE will continue to monitor any development and will update interested parties when the situation changes.
 
Status Suspended
Technology type Medicine
Decision Selected
Process STA Standard
ID number 4044

Project Team

Project lead Leena Issa

Email enquiries

External Assessment Group BMJ Technology Assessment Group (BMJ-TAG), BMJ

Stakeholders

Companies sponsors Merck Sharpe and Dohme
Others Department of Health and Social Care
  NHS England
Patient carer groups Mesothelioma UK
Professional groups Association of Cancer Physicians
  British Thoracic Oncology Group
  British Thoracic Society
  Cancer Research UK
  Royal College of Physicians
  Royal College of Radiologists
Associated public health groups None
Comparator companies Aspire Pharma (pemetrexed) (confidentiality agreement not signed, not participating)
  Bristol Myers Squibb (ipilimumab, nivolumab) (confidentiality agreement signed, participating)
  Dr. Reddy’s Laboratories (UK) (pemetrexed) (confidentiality agreement not signed, not participating)
  Eli Lilly (pemetrexed) (confidentiality agreement not signed, not participating)
  Genus (pemetrexed) (confidentiality agreement not signed, not participating)
  Hospira (carboplatin, cisplatin) (confidentiality agreement not signed, not participating)
  Pfizer (pemetrexed) (confidentiality agreement not signed, not participating)
  Sandoz (cisplatin, pemetrexed) (confidentiality agreement not signed, not participating)
  Seacross Pharmaceuticals (pemetrexed) (confidentiality agreement not signed, not participating)
  Sun Pharmaceuticals (pemetrexed) (confidentiality agreement not signed, not participating)
  Zentiva (pemetrexed) (confidentiality agreement not signed, not participating)
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
  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
03 February 2025 Suspended. For information, the company have advised that the wording of the marketing authorisation for pembrolizumab with pemetrexed and platinum-based chemotherapy for untreated unresectable advanced malignant pleural mesothelioma is still to be determined and therefore they have requested a temporary suspension of this appraisal while this issue is resolved. NICE will continue to monitor any development and will update interested parties when the situation changes.
24 July 2024 Following a request from the company, the timelines for this appraisal have been revised. The committee meeting will be held on 12 March 2025.
12 June 2024 Invitation to participate
17 January 2024 - 14 February 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 4044
17 January 2024 - 14 February 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 4044
17 January 2024 In progress. Scoping commencing

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