Johnson & Johnson (JNJ) announces U.S. FDA Approval of RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) as First and Only Dual-Targeted Therapy for Advanced Head and Neck Cancer
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The approval covers the second-line treatment of recurrent or metastatic disease and marks the first advancement in that setting in years. The dual-targeted regimen combines amivantamab with hyaluronidase, distinguishing it from existing single-agent approaches in a patient population with limited options. J&J will now look to confirmatory trial data to convert the accelerated approval into full clearance, while investors watch uptake in the second-line setting and any label expansion.
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RYBREVANT FASPRO, Johnson & Johnson (JNJ), U.S. FDA, amivantamab, hyaluronidase-lpuj
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