Suggested remit: To appraise the clinical and cost effectiveness of mobocertinib within its marketing authorisation for treating EGFR Exon 20 insertion-positive non-small-cell lung cancer.
 
Status In progress
Process STA 2018
ID number 3984

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Timeline

Key events during the development of the guidance:

Date Update
10 September 2021 - 08 October 2021 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
24 May 2021 In progress. DHSC referral received

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