Suggested remit: To appraise the clinical and cost effectiveness of lenalidomide with rituximab within its marketing authorisation for untreated follicular lymphoma.

Please note that following on from information provided to NICE by the company in July 2018, the appraisal of Lenalidomide for untreated follicular lymphoma [ID1245] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.

Status:
Discontinued
Decision:
Prioritised
Process:
TA
ID number:
1245

Project Team

Project lead
Michelle Adhemar

Email enquiries

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

Timeline

Key events during the development of the guidance:

Date Update
20 January 2023 Discontinued. Please note that following on from information provided to NICE by the company in July 2018, the appraisal of Lenalidomide for untreated follicular lymphoma [ID1245] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
01 August 2018 Suspended. Company update
01 August 2018 Note added to the project documents
08 June 2018 - 06 July 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators
27 June 2018 In progress. DHSC referral received

For further information on our processes and methods, please see our CHTE processes and methods manual