Amivantamab (Rybrevant®). HTA ID: 24032

Assessment Status Rapid Review Complete
HTA ID 24032
Drug Amivantamab
Brand Rybrevant®
Indication Amivantamab (Rybrevant®) in combination with carboplatin and pemetrexed is indicated for the first-line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) with activating epidermal growth factor receptor (EGFR) Exon 20 insertion
Assessment Process
Rapid review commissioned 31/07/2024
Rapid review completed 30/09/2024
Rapid review outcome A full HTA is recommended to assess the clinical effectiveness and cost effectiveness of amivantamab for this indication compared with the current standard of care.