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FDA to Review Applications for Potential Approval of Rybrevant for NSCLC Subset
January 2nd 2024The pharmaceutical company submitted applications for the FDA to consider approval of Rybrevant plus lazertinib for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer with EGFR exon 19 deletions or L858 substitution mutations.
Novel HER3-Directed Therapy Granted Priority Review for Previously Treated NSCLC
December 28th 2023The FDA granted priority review of patritumab deruxtecan for the treatment of locally advanced or metastatic EGFR-mutated non-small cell lung cancer previously treated with two or more systemic therapies.