Exon 20 insertion targeting Exkivity comes to Korea
By Eo, Yun-Ho | translator Alice Kang
22.03.14 17:47:08
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Takeda Pharmaceuticals Korea submits application to MFDS
Is different from ¡®Ryvrevant¡¯ being an oral administration form
According to industry sources, Takeda Pharmaceuticals Korea recently submitted an application for the marketing authorization of ¡®Exkivity (mobocertinib).¡¯ The drug is expected to be approved within the year at the earliest.
Exkivity was approved in the US in September last year as a non-small cell lung cancer (NSCLC) treatment that targets EGFR Exon20 insertion mutations like Janssen¡¯s ¡®Ryvrevant (amivantamab)¡¯ that was approved last month.
Unlike Exkivity, Ryvrevant has the strength of being an oral tablet. Exkivity was granted priority review and received Breakthrough Therapy Designation, Fast Track
Eo, Yun-Ho(unkindfish@dailypharm.com)
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