| Assessment Status | Rapid Review Complete |
| HTA ID | - |
| Drug | Lenvatinib |
| Brand | Lenvima® |
| Indication | As monotherapy for the treatment of adult patients with advanced or unresectable HCC who have received no prior systemic therapy. |
| Assessment Process | |
| Rapid review commissioned | 07/08/2018 |
| Rapid review completed | 16/08/2018 |
| Rapid review outcome | A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of lenvatinib compared with the current standard of care, on the basis of the proposed price relative to currently available therapies. |
The HSE has approved reimbursement following confidential price negotiations May 2021.