| Assessment Status | Assessment process complete |
| HTA ID | - |
| Drug | Osimertinib |
| Brand | Tagrisso® |
| Indication | As monotherapy for the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating epidermal growth factor receptor (EGFR) mutations. |
| Assessment Process | |
| Rapid review commissioned | 19/07/2018 |
| Rapid review completed | 07/08/2018 |
| Rapid review outcome | A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of osimertinib for the first-line treatment of adult patients with locally advanced or metastatic NSCLC with activating EGFR mutations compared with the current standard of care. |
| Full pharmacoeconomic assessment commissioned by HSE | 28/08/2018 |
| Pre-submission consultation with Applicant | 08/10/2018 |
| Full submission received from Applicant | 21/01/2019 |
| Preliminary review sent to Applicant | 13/05/2019 |
| NCPE assessment re-commenced | 28/05/2019 |
| Factual accuracy sent to Applicant | 19/07/2019 |
| NCPE assessment re-commenced | 30/07/2019 |
| NCPE assessment completed | 06/08/2019 |
| NCPE assessment outcome | The NCPE recommends that osimertinib 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; October 2020
