To appraise the clinical and cost effectiveness of DCVax-L for newly diagnosed glioblastoma multiforme.

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:
836

Email enquiries

If you have any queries please email scheduling@nice.org.uk

Stakeholders

Companies sponsors
Northwest Biotherapeutics (DCVax-L)
Others
Department of Health and Social Care
 
NHS England
 
Welsh Government
Patient carer groups
Brain Tumour Charity
 
Brainstrust
 
International Brain Tumour Alliance (IBTA)
Professional groups
Association of British Neurologists
 
Association of Cancer Physicians
 
Cancer Research UK
 
Royal College of Physicians
 
Royal College of Radiologists
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
 
Welsh Health Specialised Services Committee
Relevant research groups
Institute of Cancer Research

Timeline

Key events during the development of the guidance:

Date Update
02 April 2025 Note - Note added to the project documents
05 March 2024 Note - Note added to the project documents
23 December 2022 Note added to the project documents
22 December 2022 In progress
19 September 2018 Note added to the project documents
14 June 2018 Invitation to participate
03 April 2018 - 01 May 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators
16 August 2017 Note added to the project documents
26 January 2017 - 23 February 2017 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators
22 July 2016 Referral

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