Suggested remit: To appraise the clinical and cost effectiveness of brentuximab vedotin with etoposide, cyclophosphamide, doxorubicin, dacarbazine and dexamethasone within its marketing authorisation for treating untreated advanced classical Hodgkin lymphoma.
- 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:
- 6437
Provisional Schedule
- Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6437:
- 13 March 2026 - 14 April 2026
- Expected publication:
- 06 May 2027
Project Team
- Project lead
- Emily Richards
Email enquiries
If you have any queries please email scopingta@nice.org.uk
Timeline
Key events during the development of the guidance:
| Date | Update |
|---|---|
| 13 March 2026 | In progress. Scoping commencing |
| 12 December 2024 | Referral |
| 28 February 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