Suggested remit: To appraise the clinical and cost effectiveness of tucatinib with trastuzumab and capecitabine within its marketing authorisation for treating HER2-positive unresectable or metastatic advanced breast cancer after 2 or more anti-HER2 therapies.
 
Status In progress
Process STA 2018
ID number 3828

Project Team

Project lead Michelle Adhemar

Email enquiries

Timeline

Key events during the development of the guidance:

Date Update
09 November 2020 - 07 December 2020 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
05 August 2020 In progress. DHSC referral received

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