Merck Announces FDA Breakthrough Therapy Designation for Investigational Therapy Tepotinib in Patients with Metastatic NSCLC with METex14 Skipping Alterations

– Investigational oral MET inhibitor has previously received SAKIGAKE ‘fast-track’ regulatory designation in Japan – MET exon 14 skipping alterations and MET amplifications are present in 3-5% of non-small …

source https://finance.yahoo.com/news/merck-announces-fda-breakthrough-therapy-063000846.html?.tsrc=rss

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