Janssen-Cilag International, a Johnson & Johnson company, announced that the Committee for Medicinal Products for Human Use of the European Medicines Agency has recommended the approval of a type II extension of indication for Rybrevant in combination with chemotherapy for the treatment of adult patients with advanced non-small cell lung cancer with epidermal growth factor receptor exon 19 deletions or exon 21 L858R substitution mutations, after failure of prior therapy including an EGFR tyrosine kinase inhibitor.
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