| Assessment Status | NCPE Assessment Process Complete |
| HTA ID | 22043 |
| Drug | Polatuzumab vedotin |
| Brand | Polivy® |
| Indication | In combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (pola-R-CHP) is indicated for the treatment of adult patients with previously untreated diffuse large B-cell lymphoma (DLBCL). |
| Assessment Process | |
| Rapid review commissioned | 27/06/2022 |
| Rapid review completed | 27/07/2022 |
| Rapid review outcome | A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of pola-R-CHP compared with the current standard of care. |
| Full pharmacoeconomic assessment commissioned by HSE | 31/08/2022 |
| Pre-submission consultation with Applicant | 08/11/2022 |
| Full submission received from Applicant | 26/01/2023 |
| Preliminary review sent to Applicant | 20/07/2023 |
| NCPE assessment re-commenced | 18/08/2023 |
| Factual accuracy sent to Applicant | 16/11/2023 |
| NCPE assessment re-commenced | 23/11/2023 |
| NCPE assessment completed | 05/12/2023 |
| NCPE assessment outcome | The NCPE recommends that polatuzumab vedotin (Polivy®) not be considered for reimbursement unless 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.
The HSE has approved reimbursement following confidential price negotiations. August 2024
