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    Home > Medical News > Latest Medical News > Keystone Pharmaceuticals' Apoitini listing application was given priority review.

    Keystone Pharmaceuticals' Apoitini listing application was given priority review.

    • Last Update: 2020-08-08
    • Source: Internet
    • Author: User
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    Apertinib, a KIT/PDGFRA inhibitor developed by Blueprint Medicines, was approved by the FDA in the United States in January 2020 for the treatment of advanced GIST adult patients carrying PDGFRA exon 18 mutations, including PDGFRA D842V.
    Cornerstone Pharmaceuticals has entered into exclusive cooperation and licensing with Blueprint Medicines, which has obtained exclusive development and commercialization of a number of drugs, including Apertinib, in Greater China.
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