Serplulimab (Hetronifly®). HTA ID: 25021

Assessment Status Rapid Review Complete
HTA ID 25021
Drug Serplulimab
Brand Hetronifly®
Indication Serplulimab (Hetronifly®) in combination with carboplatin and etoposide is indicated for the first-line treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC).
Assessment Process
Rapid review commissioned 10/03/2025
Rapid review completed 15/04/2025
Rapid review outcome A full HTA is not recommended. The NCPE recommends that serplulimab not be considered for reimbursement at the submitted price*.

*This recommendation should be considered while also having regard to the criteria specified in the Health (Pricing and Supply of Medical Goods) Act 2013.

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.