| Assessment Status | NCPE Assessment Process complete |
| HTA ID | 23011 |
| Drug | Trastuzumab deruxtecan |
| Brand | Enhertu® |
| Indication | Trastuzumab deruxtecan as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic HER2 low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy. |
| Assessment Process | |
| Rapid review commissioned | 20/02/2023 |
| Rapid review completed | 16/03/2023 |
| Rapid review outcome | A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of trastuzumab deruxtecan compared with the current standard of care. |
| Full pharmacoeconomic assessment commissioned by HSE | 30/03/2023 |
| Pre-submission consultation with Applicant | 30/05/2023 |
| Full submission received from Applicant | 20/09/2023 |
| Preliminary review sent to Applicant | 25/03/2024 |
| NCPE assessment re-commenced | 26/04/2024 |
| Factual accuracy sent to Applicant | 20/08/2024 |
| NCPE assessment re-commenced | 28/08/2024 |
| NCPE assessment completed | 30/09/2024 |
| NCPE assessment outcome | The NCPE recommends that trastuzumab deruxtecan be considered for reimbursement if cost-effectiveness can be improved relative to existing treatments*. |
*This recommendation should be considered while also having regard to the criteria specified in the Health (Pricing and Supply of Medical Goods) Act 2013.
