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 Selected
Process TA
ID number 1245

Project Team

Project lead Michelle Adhemar

Email enquiries

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 The Department for Health and Social Care has asked NICE to carry out a Single Technology Appraisal (STA) of lenalidomide within its marketing authorisation for treating follicular, untreated lymphoma. Following a recent update from the company, NICE has decided to suspend this appraisal on its work programme. As the appraisal has been referred, NICE will continue to monitor any developments and will provide a further update in due course.
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

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