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The peptides should be reevaluated under a better process by the Pharmacy Compounding Advisory Committee, said Davis, referring to a panel that advises the FDA on issues related to drug compounding

The approval was based on results from the randomized, open-label, multicenter, phase III PALOMA-3 clinical trial, which analyzed the safety and efficacy of amivantamab and hyaluronidase-lpuj in patients with locally advanced or metastatic NSCLC that had either an exon 19 deletion or an exon 21 L858R substitution mutation in the EGFR gene

As a result of this combinational therapy, the median overall survival time was 14.2 months and the median progression-free survival time was 9.6 months