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FDA Grants Breakthrough Therapy Designation to Furmonertinib for EGFR Exon 20 Insertion+ NSCLC

The FDA has granted breakthrough therapy designation to furmonertinib for use as a potential therapeutic option in patients with previously untreated, locally advanced or metastatic nonsquamous non–small cell lung cancer harboring EGFR exon 20 insertion mutations.

South koreaStuart lutzkerArrivent biopharma incArrivent biopharmaLung cancer world conferenceLung cancershowedVent biopharmaInternational associationLung cancerEpidermal growth factor receptorBreakthrough therapy designation

ArriVent raises $150M to bring Chinese drugs to Western markets

ArriVent raises $150M to bring Chinese drugs to Western markets
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