Suggested remit: To appraise the clinical and cost effectiveness of oral paclitaxel with encequidar within its marketing authorisation for treating advanced breast cancer.
For information, the company have advised that they are no longer pursuing a Marketing Authorisation Application from the Medicines and Healthcare products Regulatory 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.
 
Status Suspended
Technology type Medicine
Decision Selected
Reason for decision Anticipate the topic will be of importance to patients, carers, professionals, commissioners and the health of the public to ensure clinical benefit is realised, inequalities in use addressed, and help them make the best use of NHS resources
Further information DHSC referral received
Process TA
ID number 5111

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Timeline

Key events during the development of the guidance:

Date Update
17 February 2023 Suspended. For information, the company have advised that they are no longer pursuing a Marketing Authorisation Application from the Medicines and Healthcare products Regulatory 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.
07 October 2022 As you will be aware the Department for Health and Social Care has asked NICE to carry out a Single Technology Appraisal of Paclitaxel with encequidar for treating advanced breast cancer. Please note that following on from advice received from the company the timelines for this appraisal are to be confirmed. Further information regarding the scheduling of this appraisal will be available in due course.
08 August 2022 - 06 September 2022 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
07 July 2022 In progress

For further information on our processes and methods, please see our CHTE processes and methods manual