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P-I/II (RAMP 203) trial assessed the regimen defactinib in therapy-nave & experienced KRAS G12C mutant NSCLC Company: AbbVie Product: Emrelis Active Ingredient: Telisotuzumab vedotin-tllv Disease: NSCLC with High c-Met Protein Overexpression Date: May 14, 2025 Shots: The US FDA has granted accelerated approval to Emrelis (telisotuzumab vedotin-tllv) for treatment-experienced pts with locally advanced or metastatic, c-Met overexpressing, non-squamous NSCLC Approval was backed by an ongoing P-II (LUMINOSITY) study assessing Emrelis as 2L/3L treatment of c-Met overexpressing NSCLC

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