Suggested remit: To appraise the clinical and cost effectiveness of veliparib within its marketing authorisation for treating BRCA-positive, human epidermal growth factor 2 (HER2)-negative, breast advanced cancer.
Following on from information provided to NICE by the company in March 2021, the appraisal of Veliparib in combination for treating BRCA-positive, HER2-negative breast advanced cancer [ID1404] 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:
- Prioritised
- Process:
- TA
- ID number:
- 1404
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Timeline
Key events during the development of the guidance:
| Date | Update |
|---|---|
| 21 November 2022 | Note added to the project documents |
| 21 November 2022 | Discontinued. Following on from information provided to NICE by the company in March 2021, the appraisal of Veliparib in combination for treating BRCA-positive, HER2-negative breast advanced cancer [ID1404] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued. |
| 06 April 2021 | Suspended. For information, the company have advised that they are no longer pursuing a Marketing Authorisation Application 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. |
| 20 December 2019 | Note added to the project documents |
| 23 October 2019 - 20 November 2019 | Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators |
| 13 February 2018 | In progress. Topic referred |
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