Suggested remit: To appraise the clinical and cost effectiveness of asciminib within its marketing authorisation for treating Philadelphia-chromosome-positive chronic myeloid leukaemia (CML) in the chronic phase after two or more tyrosine kinase inhibitors.
 
Status In progress
Process STA 2018
ID number 3813

Provisional Schedule

Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators 27 May 2021 - 25 June 2021

Project Team

Project lead Emily Richards

Email enquiries

Timeline

Key events during the development of the guidance:

Date Update
29 October 2018 In progress. DHSC referral received

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