Suggested remit: To appraise the clinical and cost effectiveness of avelumab within its marketing authorisation for treating non-small-cell lung cancer after platinum-based chemotherapy.

Following on from information provided to NICE by the company in January 2020, the appraisal of Avelumab for treating non-small-cell lung cancer after platinum-based chemotherapy [ID1146] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.

Status:
Discontinued
Technology type:
Medicine
Decision:
Prioritised
Process:
TA
ID number:
1146

Email enquiries

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

Timeline

Key events during the development of the guidance:

Date Update
22 November 2022 Discontinued. Following on from information provided to NICE by the company in January 2020, the appraisal of Avelumab for treating non-small-cell lung cancer after platinum-based chemotherapy [ID1146] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
17 January 2020 Note added to the project documents
17 January 2020 Suspended. Referred February 13 2018
25 April 2018 - 24 May 2018 Consultation on suggested remit, draft scope and provisional matrix of consultees and commentators
13 February 2018 In progress. DHSC referral received

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