Suggested remit: To appraise the clinical and cost effectiveness of sebetralstat within its marketing authorisation for treating acute attacks of hereditary angioedema.

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:
6284

Provisional Schedule

Committee meeting: 1:
14 October 2025
Expected publication:
17 December 2025

Project Team

Project lead
Leena Issa

Email enquiries

If you have any queries please email [email protected]


External Assessment Group:
Kleijnen Systematic Reviews Ltd

Stakeholders

Companies sponsors
KalVista (sebetralstat)
 
British Society for Allergy & Clinical Immunology
 
BSI Clinical Immunology Professional Network (BSI-CIPN)
 
Royal College of Pathologists
 
Royal College of Physicians
Others
Department of Health and Social Care
 
NHS England
Patient carer groups
HAE UK
Associated public health groups
None
Comparator companies
Takeda (cinryze, icatibant) (confidentiality agreement signed, participating)
 
Accord (icatibant) (confidentiality agreement not signed, not participating)
 
Celix Pharma (icatibant) (confidentiality agreement not signed, not participating)
 
Cipla (icatibant) (confidentiality agreement not signed, not participating)
 
CSL Behring (Berinert) (confidentiality agreement not signed, not participating)
 
Ethypharm (icatibant) (confidentiality agreement not signed, not participating)
 
Glenmark Pharmaceutical (icatibant) (confidentiality agreement not signed, not participating)
 
Martindale Pharmaceuticals (icatibant) (confidentiality agreement not signed, not participating)
 
Pharming Group N.V (ruconest) (confidentiality agreement not signed, not participating)
 
Piramal Critical Care (icatibant) (confidentiality agreement not signed, not participating)
 
Sandoz (icatibant) (confidentiality agreement not signed, not participating)
 
Wockhardt (icatibant) (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
 
NHS Wales Joint Commissioning Committee
 
Scottish Medicines Consortium
 
Welsh Government
Relevant research groups
None

Timeline

Key events during the development of the guidance:

Date Update
14 March 2025 Invitation to participate
28 June 2024 - 26 July 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6284
28 June 2024 In progress. Scoping commenced.
28 April 2023 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