J&J submits FDA application for RYBREVANT FASPRO in advanced head and neck cancer

Johnson & Johnson

Johnson & Johnson

JNJ

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  • Johnson & Johnson filed a supplemental Biologics License Application with the U.S. FDA for subcutaneous RYBREVANT FASPRO in advanced head and neck cancer.
  • The filing follows Breakthrough Therapy Designation, supported by OrigAMI-4 data showing a 42% confirmed response rate in previously treated patients.


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