- 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:
- 6294
Project Team
- Project lead
- Leena Issa
Email enquiries
If you have any queries please email [email protected]
- External Assessment Group:
- Southampton Health Technology Assessment Centre (SHTAC), University of Southampton
Stakeholders
- Companies sponsors
- Merck (avelumab)
- Others
- Department of Health and Social Care
- NHS England
- Patient carer groups
- Action Kidney Cancer
- Kidney Cancer UK
- Kidney Research UK
- Professional groups
- Association of Cancer Physicians
- British Uro-oncology Group
- Cancer Research UK
- Royal College of Physicians
- Royal College of Radiologists
- Associated public health groups
- None
- Comparator companies
- Bristol Myers Squibb Pharmaceuticals (ipilimumab, nivolumab) (confidentiality agreement signed, participating)
- Eisai (lenvatinib) (confidentiality agreement signed, participating)
- Ipsen (cabozantinib) (confidentiality agreement signed, participating)
- Merck Sharp & Dohme (UK) (pembrolizumab) (confidentiality agreement signed, participating)
- Pfizer (sunitinib) (confidentiality agreement signed, participating)
- Accord-UK (sunitinib) (confidentiality agreement not signed, not participating)
- Dr Reddy’s Laboratories (sunitinib) (confidentiality agreement not signed, not participating)
- Eusa Pharma (tivozanib) (confidentiality agreement not signed, not participating)
- MSN laboratories (sunitinib) (confidentiality agreement not signed, not participating)
- Novartis (pazopanib) (confidentiality agreement not signed, not participating)
- Piramal Critical Care (sunitinib) (confidentiality agreement not signed, not participating)
- Sandoz (sunitinib) (confidentiality agreement not signed, not participating)
- Teva UK (sunitinib) (confidentiality agreement not signed, not participating)
- Viatris UK Healthcare (sunitinib) (confidentiality agreement not signed, not participating)
- Zentiva (sunitinib) (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
- NHS Wales Joint Commissioning Committee
- Scottish Medicines Consortium
- Welsh Government
- Relevant research groups
- Institute of Cancer Research
Timeline
Key events during the development of the guidance:
Date | Update |
---|---|
09 April 2025 | Committee meeting |
05 September 2024 | Invitation to participate |
05 September 2024 | In progress. Invitation to participate issued. |
23 July 2024 - 13 August 2024 | Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators |
12 July 2024 | 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