Durvalumab (Imfinzi®). HTA ID: 26018

Assessment Status Rapid Review Complete
HTA ID 26018
Drug Durvalumab
Brand Imfinzi®
Indication Durvalumab (Imfinzi®) in combination with carboplatin and paclitaxel is indicated for the first-line treatment of adults with primary advanced or recurrent endometrial cancer who are candidates for systemic therapy, followed by maintenance treatment with durvalumab as monotherapy in endometrial cancer that is mismatch repair deficient.
Assessment Process
Rapid review commissioned 10/04/2026
Rapid review completed 15/05/2026
Rapid review outcome A full HTA is not recommended. The NCPE recommends that durvalumab not be considered for reimbursement at the submitted price*.

Next steps: The NCPE Assessment Report and recommendation, will be considered by the HSE when making their decision on reimbursement, while also having regard to the criteria specified in the Health (Pricing and Supply of Medical Goods) Act 2013.

Further information on this process may be found here

Further information on the status of this decision may be found here