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February 18, 2026

J&J’s Rybrevant Faspro gains FDA approval for new dosing in NSCLC

Johnson & Johnson (J&J) has received the US Food and Drug Administration (FDA) approval for a new monthly dosing schedule for the combination therapy Rybrevant Faspro (amivantamab and hyaluronidase-lpuj) to treat patients with advanced, epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC).

The PALOMA-2 study showed monthly Rybrevant Faspro with Lazcluze achieved high response in untreated advanced EGFR-mutated NSCLC. Credit: Arif biswas/Shutterstock.com.