The FDA in the United States has accepted a supplementary marketing application for the treatment of locally advanced or metastatic solid tumor patients with NTRK positivity using reprotinib
因醉鞭名马幌
发表于 2024-2-16 10:13:03
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According to the official WeChat account of Zaiding Pharmaceuticals, its partner, Bristol Myers Squibb, announced on February 14th that the US Food and Drug Administration (FDA) has accepted Augtro's supplementary new drug application (sNDA) for the treatment of solid tumor patients aged 12 years and above who have neurotrophic tyrosine receptor kinase (NTRK) gene fusion and are locally advanced or metastatic, Or due to severe illness, surgery cannot remove it. The FDA has granted the application priority review qualification, and the target action date for the Prescription Drug User Payment Act (PDUFA) is June 15, 2024.
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声明:该文观点仅代表作者本人,本文不代表CandyLake.com立场,且不构成建议,请谨慎对待。
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