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SUMMARY
- RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) for subcutaneous (SC) administration is a coformulation of amivantamab with recombinant human hyaluronidase PH20 (rHuPH20).1
- Of the 206 patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) treated with RYBREVANT FASPRO in combination with LAZCLUZE, 35% were aged ≥65 years and 9% were aged ≥75 years.2
- The safety of RYBREVANT FASPRO in combination with other antineoplastic drugs or as a single agent for its approved indications has been established in adequate and well-controlled studies of RYBREVANT intravenous (IV) in combination with other antineoplastic drugs and as a single agent.2
- Of the 421 patients with locally advanced or metastatic NSCLC treated with RYBREVANT IV in combination with LAZCLUZE in the MARIPOSA study, 45% were aged ≥65 years and 12% were aged ≥75 years.
- Of the 130 patients with locally advanced or metastatic NSCLC treated with RYBREVANT IV in combination with carboplatin and pemetrexed in the MARIPOSA-2 study, 40% were aged ≥65 years and 10% were aged ≥75 years.
- Of the 151 patients with locally advanced or metastatic NSCLC treated with RYBREVANT IV in combination with carboplatin and pemetrexed in the PAPILLON study, 37% were aged ≥65 years and 8% were aged ≥75 years.
- Of the 302 patients with locally advanced or metastatic NSCLC treated with RYBREVANT IV as a single agent in the CHRYSALIS study, 39% were aged ≥65 years and 11% were aged ≥75 years.
- No clinically important differences in safety or efficacy were observed between patients who were aged ≥65 years and younger patients.2
- Please refer to RYBREVANT FASPRO product labeling for additional information.2
LITERATURE SEARCH
A literature search of MEDLINE®, Embase®, BIOSIS Previews®, and Derwent Drug File (and/or other resources, including internal/external databases) was conducted on 08 December 2025.