?The U.S. Food and Drug Administration (FDA) approved TEPMETKO (tepotinib) for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) harboring mesenchymalepithelial transition (MET) exon 14 skipping alterations.
Merck, a leading science and technology company, today announced that the US Food and Drug Administration (FDA) has approved TEPMETKO? (tepotinib) following Priority Review for the treatment of adult patients with metastatic non-small cell lung cancer ...
Merck, a leading science and technology company, today announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) has approved TEPMETKO?* (tepotinib) for the treatment of patients with unresectable, advanced or recurrent non-small cell lung