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FDA grants accelerated approval to capmatinib (Tabrecta) for metastatic non-small cell lung cancer

11 May 2020 9:06 AM | Nathan Strunk (Administrator)

The U.S. Food and Drug Administration granted accelerated approval to capmatinib (TABRECTA, Novartis) for adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have a mutation that leads to mesenchymal-epithelial transition (MET) exon 14 skipping as detected by an FDA-approved test. Read full press release

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