Following on from information provided to NICE by the company in October 2021 the appraisal of Azacitidine for treating relapsed or refractory angioimmunoblastic T-cell lymphoma [ID3864] 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 | 3864 |
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Timeline
Key events during the development of the guidance:
| Date | Update |
|---|---|
| 21 December 2022 | Discontinued. Following on from information provided to NICE by the company in October 2021 the appraisal of Azacitidine for treating relapsed or refractory angioimmunoblastic T-cell lymphoma [ID3864] was suspended from NICE’s work programme. As no further information has been received from the company the topic has been discontinued. |
| 08 July 2022 | 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 (MHRA) 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. |
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