November 6, 2026Stocks·Bullish·regulatory
FDA grants accelerated approval for J&J's RYBREVANT FASPRO in head and neck squamous cell carcinoma
Johnson & Johnson announced the FDA granted accelerated approval for RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) for adult patients with recurrent or metastatic head and neck squamous cell carcinoma whose disease progressed on or after platinum-based chemotherapy and an anti-PD-(L)1 antibody.
Detected & updated continuously · Source: Nebula
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Johnson & JohnsonFood and Drug Administration