Suggested remit: To appraise the clinical and cost effectiveness of atogepant within its marketing authorisation for treating migraine.

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:
6615

Provisional Schedule

Expected publication:
09 July 2026

Project Team

Project lead
Kate Moore

Email enquiries

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


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

Stakeholders

Companies sponsors
AbbVie (atogepant)
Others
Department of Health and Social Care
 
NHS England
Patient carer groups
Migraine Trust
Professional groups
Royal College of Physicians
 
UK Clinical Pharmacy Association
Associated public health groups
None
Comparator companies
Pfizer (rimegepant) (confidentiality agreement signed, 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
 
NHS Wales Joint Commissioning Committee
 
Scottish Medicines Consortium
 
Welsh Government
Relevant research groups
None

Related links

Timeline

Key events during the development of the guidance:

Date Update
06 January 2026 Invitation to participate
23 October 2025 - 20 November 2025 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
23 October 2025 In progress. Scoping commenced.
18 August 2025 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