FDA grants accelerated approval to tepotinib for metastatic non-small cell lung cancer

FDA

3 February 2021 - Today the FDA granted accelerated approval to tepotinib (Tepmetko, EMD Serono) for adult patients with metastatic non-small cell lung cancer harbouring mesenchymal-epithelial transition (MET) exon 14 skipping alterations.

Efficacy was demonstrated in the VISION trial, a multicenter, non-randomized, open-label, multi-cohort study enrolling 152 patients with advanced or metastatic non-small-cell lung cancer with MET exon 14 skipping alterations.

Read FDA press release

Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , US