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