Pfizer has indicated that they will not be making a submission to NICE for the above indication until the outcome of the palboclicib plus an aromatase inhibitor appraisal [ID915] is final. In the meantime appraisal [ID916] will be suspended while NICE considers the options for rescheduling.
| Status | Suspended |
| Process | STA |
| ID number | 916 |
Project Team
| Project lead | Liv Gualda |
Email enquiries
- If you have any queries please email tacomma@nice.org.uk
Timeline
Key events during the development of the guidance:
| Date | Update |
|---|---|
| 03 February 2017 | Suspended, Pfizer has indicated that they will not be making a submission to NICE for the above indication until the outcome of the palboclicib plus an aromatase inhibitor appraisal [ID915] is final. In the meantime appraisal [ID916] will be suspended while NICE considers the options for rescheduling. |
| 23 November 2016 | The technology appraisal of palbociclib in combination with fulvestrant for hormone-receptor positive, HER2-negative breast cancer after endocrine therapy [ID916] has now been rescheduled. The first committee meeting will take place in June 2017. |
| 20 October 2016 | The technology appraisal of palbociclib in combination with fulvestrant for hormone-receptor positive, HER2-negative breast cancer after endocrine therapy [ID916] has been suspended at the request of Pfizer. The Company submission of a value proposition for palbociclib after endocrine therapy will follow after the outcome of the appraisal of palbociclib for previously untreated disease [ID915] is known. |
| 06 October 2016 | Invitation to participate |
| 13 May 2016 | Referral |
For further information on how we develop guidance, please see our page about NICE technology appraisal guidance