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    "name": "Molecular Oncology Almanac",
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  "data": [
    {
      "id": "ind:fda.gleevec:5",
      "indication": "Gleevec is a kinase inhibitor indicated for the treatment of adult patients with aggressive systemic mastocytosis (ASM) without the D816V c-Kit mutation or with c-Kit mutational status unknown.",
      "initial_approval_date": "2006-10-19",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2006/021588s011s012s013s014s017lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to imatinib for the treatment of adult patients with aggressive systemic mastocytosis (ASM) without the D816V c-Kit mutation or with c-Kit mutational status unknown.",
      "raw_biomarkers": "without the D816V c-Kit mutation or with the c-Kit mutational status unknown",
      "raw_cancer_type": "aggressive systemic mastocytosis (ASM)",
      "raw_therapeutics": "Gleevec (imatinib)",
      "icd10": null,
      "regimen_code": null,
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      "date_accelerated_approval": null,
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        "id": "doc:fda.gleevec",
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        "name": "Gleevec (imatinib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Novartis Pharmaceuticals Corporation. Gleevec (imatinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/021588s062lbl.pdf. Revised August 2022. Accessed October 30, 2024.",
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            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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}