Suggested remit: To appraise the clinical and cost effectiveness of atezolizumab with cobimetinib and vemurafenib within its marketing authorisation for treating unresectable or metastatic BRAF V600 mutation-positive melanoma.
Following on from information provided to NICE by the company in January 2020, the appraisal of Atezolizumab with cobimetinib and vemurafenib for treating unresectable or metastatic BRAF V600 mutation-positive melanoma [ID1674] 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 Selected
Process TA
ID number 1674

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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 Atezolizumab with cobimetinib and vemurafenib for treating unresectable or metastatic BRAF V600 mutation-positive melanoma [ID1674] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
29 January 2020 Suspended. Topic is suspended
29 January 2020 The Department for Health and Social Care has asked NICE to carry out a Single Technology Appraisal of atezolizumab with cobimetinib and vemurafenib for treating unresectable or metastatic BRAF V600 mutation-positive melanoma. Please note that following on from advice received from the company regarding the regulatory timelines , NICE has decided to suspend this appraisal from its current work programme. As this appraisal has been referred NICE will continue to monitor any development and will update interested parties as and when the situation changes.
02 October 2019 - 30 October 2019 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
31 July 2017 In progress. DHSC Referral Received

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