Following on from information provided to NICE by the company in February 2021, the appraisal of Brigatinib for treating ALK-positive advanced non-small-cell lung cancer after alectinib or ceritinib [ID2702] 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 2702

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Timeline

Key events during the development of the guidance:

Date Update
21 November 2022 Following on from information provided to NICE by the company in February 2021, the appraisal of Brigatinib for treating ALK-positive advanced non-small-cell lung cancer after alectinib or ceritinib [ID2702] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
21 November 2022 Discontinued. Following on from information provided to NICE by the company in February 2021, the appraisal of Brigatinib for treating ALK-positive advanced non-small-cell lung cancer after alectinib or ceritinib [ID2702] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued.
26 February 2021 Suspended. Topic is suspended
26 February 2021 As you will be aware, the Department for Health and Social Care has asked NICE to carry out a Single Technology Appraisal of brigatinib for treating ALK-positive advanced non-small-cell lung cancer after alectinib or ceritinib. For information, the company have advised that they are no longer pursuing a Marketing Authorisation Application at this time, from the European Medicines Agency for this indication at this time. Therefore, 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 if the situation changes.
24 January 2020 In progress. Topic is in progress

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