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 | Scoping commencing |
Process | Pathways Pilot |
ID number | 6186 |
Project Team
Project lead | Jeremy Powell |
Email enquiries
- If you have any queries please email TAteam2@nice.org.uk
External Assessment Group | Peninsula Technology Assessment Group (PenTAG), University of Exeter |
Stakeholders
Companies sponsors | Ipsen (cabozantinib) |
Others | Department of Health and Social Care |
NHS England | |
Patient carer groups | Action Kidney Cancer |
Kidney Cancer UK | |
Professional groups | Association of Cancer Physicians |
British Association of Urological Surgeons | |
Cancer Research UK | |
Royal College of Physicians | |
Royal College of Radiologists | |
UK Kidney Association | |
Comparator companies | Accord Healthcare (sunitinib) (not participating) |
BMS (ipilimumab, nivolumab) | |
Dr Reddy’s Laboratories (sunitinib) (not participating) | |
Eisai (lenvatinib) | |
Eusa Pharma (tivozanib) (not participating) | |
Merck Sharp & Dohme (pembrolizumab) | |
Mylan (sunitinib) (not participating) | |
Novartis (pazopanib) | |
Piramal Critical Care (sunitinib) (not participating) | |
Pfizer (sunitinib) (not participating) | |
Sandoz (sunitinib) | |
Teva UK (sunitinib) (not participating) | |
Zentiva (sunitinib) (not participating) | |
Pathway companies: | |
Accord Healthcare (sunitinib, everolimus) (not participating) | |
BMS (ipilimumab, nivolumab) | |
Dr Reddy’s Laboratories (sunitinib, everolimus) (not participating) | |
Eisai (lenvatinib) | |
Eusa Pharma (tivozanib) (not participating) | |
Ethypharm UK (everolimus) (not participating) | |
Ipsen (cabozantinib) | |
Merck Serono (avelumab) | |
Merck Sharp & Dohme (pembrolizumab) | |
Mylan (sunitinib) (not participating) | |
Novartis (everolimus, pazopanib) | |
Piramal Critical Care (sunitinib) (not participating) | |
Pfizer (axitinib, sunitinib) (not participating) | |
Sandoz (everolimus, sunitinib) | |
Teva UK (sunitinib) (not participating) | |
Zentiva (sunitinib) (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 | |
Scottish Medicines Consortium | |
Welsh Government | |
Welsh Health Specialised Services Committee |
Timeline
Key events during the development of the guidance:
Date | Update |
---|---|
01 February 2024 | Committee meeting: 2 |
30 November 2023 | This appraisal has been developed as part of NICE's proportionate approach to technology appraisals. It is a pilot for the ‘Pathways’ approach. Further documents are published under cabozantinib with nivolumab for untreated advanced renal cell carcinoma [ID6184]. |
26 October 2023 | Committee meeting: 1 |
24 April 2023 | Assessment report sent for information |
13 February 2023 | Please note that belzutifan will not be included in the renal cell carcinoma pathways evaluation at this time. NICE and the company are continuing to liaise about scheduling for this topic and further participation in the pathway evaluations. |
13 February 2023 | Invitation to participate |
16 January 2023 (13:00) | Scoping workshop |
21 November 2022 - 19 December 2022 | Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators |
21 November 2022 | In progress |
For further information on our processes and methods, please see our CHTE processes and methods manual