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.