Lorlatinib (Lorviqua®) for 1L ALK positive NSCLC. HTA ID: 21071

Assessment Status Rapid Review Complete
HTA ID 21071
Drug Lorlatinib
Brand Lorviqua®
Indication As monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC) previously not treated with an ALK inhibitor.
Assessment Process
Rapid review commissioned 22/12/2021
Rapid review completed 13/01/2022
Rapid review outcome A full HTA is not recommended. The NCPE recommends that lorlatinib 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.

The HSE has approved reimbursement following confidential price negotiations – October 2022.