Suggested remit - To appraise the clinical and cost effectiveness of depatuxizumab mafodotin within its marketing authorisation for treating newly diagnosed EGFR-amplified glioblastoma multiforme

Following on from information provided to NICE by the company in June 2019, the appraisal of Depatuxizumab mafodotin in combination for untreated EGFR-amplified glioblastoma multiforme [ID1466] 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:
1466

Email enquiries

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

Timeline

Key events during the development of the guidance:

Date Update
10 November 2022 Discontinued. Following on from information provided to NICE by the company in June 2019, the appraisal of Depatuxizumab mafodotin in combination for untreated EGFR-amplified glioblastoma multiforme [ID1466] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
04 June 2019 Note added to the project documents
21 March 2017 Referral
21 March 2017 In progress. Topic referred

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