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The State Food and Drug Administration conditionally approved the marketing of mobosetinib succinate capsules

 Last Update: 2023-02-01
 Source: Internet
 Author: User

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Recently, the State Medical Products Administration (NMPA) conditionally approved the listing of Mobosetinib succinate capsules (trade name: ENVIRIX/EXKIVITY) declared by Takeda Pharmaceutical Co.
, Ltd.
through the priority review and approval process
.
It is indicated for adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) who progress during or after platinum-containing chemotherapy and carry an epidermal growth factor receptor (EGFR) exon 20 insertion mutation
.
Mobosetinib is an irreversible tyrosine kinase inhibitor
targeting EGFR exon 20 insertion mutations.
The launch of this drug provides a new treatment option
for patients with advanced non-small cell lung cancer who carry EGFR exon 20 insertion mutation positive.

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