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    1. United States/
    2. Janssen Submits Supplemental Biologics License Application to U.S. FDA Seeking Approval of RYBREVANT ® (amivantamab-vmjw) Plus Chemotherapy for the Treatment of Patients with EGFR-Mutated Non-Small Cell Lung Cancer Who Progressed on or after Osimertinib

    Janssen Submits Supplemental Biologics License Application to U.S. FDA Seeking Approval of RYBREVANT ® (amivantamab-vmjw) Plus Chemotherapy for the Treatment of Patients with EGFR-Mutated Non-Small Cell Lung Cancer Who Progressed on or after Osimertinib

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