{
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    "timestamp_received": "2026-04-25T12:54:16.343161+00:00Z",
    "timestamp_returned": "2026-04-25T12:54:16.347068+00:00Z",
    "trace_id": "5c873c0d-2bc5-4990-9f49-a5598b70339e"
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    "github": "https://github.com/vanallenlab/moalmanac-db",
    "name": "Molecular Oncology Almanac",
    "license": "GPL-2.0",
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    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-04-09"
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  "data": [
    {
      "id": "ind:fda.mylotarg:1",
      "indication": "MYLOTARG is a CD33-directed antibody and cytotoxic drug conjugate indicated for treatment of relapsed or refractory CD33-positive AML in adults and pediatric patients 2 years and older.",
      "initial_approval_date": "2017-09-01",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/761060lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to gemtuzumab ozogamicin for the treatment of adult and pediatric patients aged 2 years and older with relapsed or refractory CD33-positive acute myeloid leukemia (AML).",
      "raw_biomarkers": "CD33-positive",
      "raw_cancer_type": "acute myeloid leukemia",
      "raw_therapeutics": "Mylotarg (gemtuzumab ozogamicin)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
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      "date_accelerated_approval": null,
      "document": {
        "id": "doc:fda.mylotarg",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Mylotarg (gemtuzumab ozogamicin) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Wyeth Pharmaceuticals LLC. Mylotarg (gemtuzumab ozogamicin) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/761060s004lbl.pdf. Revised June 2022. Accessed October 30, 2024.",
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            "description": "The brand name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "gemtuzumab ozogamicin",
            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": "2020-06-16",
            "description": "The publication date for the document."
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            "value": "Active",
            "description": "Whether this document is Active or Deprecated within moalmanac-db."
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}