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    "timestamp_received": "2026-04-06T16:45:21.643958+00:00Z",
    "timestamp_returned": "2026-04-06T16:45:21.652462+00:00Z",
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    "name": "Molecular Oncology Almanac",
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    "url": "https://dev.moalmanac.org",
    "last_updated": "2026-03-05"
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  "data": [
    {
      "id": "ind:fda.alunbrig:0",
      "indication": "ALUNBRIG is a kinase inhibitor indicated for the treatment of adult patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) as detected by an FDA-approved test.",
      "initial_approval_date": "2020-05-22",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/208772s008lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to brigatinib for the treatment of adult patients with anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC), as detected by an FDA-approved test.",
      "raw_biomarkers": "ALK-positive",
      "raw_cancer_type": "metastatic non-small cell lung cancer",
      "raw_therapeutics": "Alunbrig (brigatinib)",
      "icd10": null,
      "regimen_code": null,
      "reimbursement_category": null,
      "reimbursement_date": null,
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      "date_regular_approval": null,
      "date_accelerated_approval": null,
      "document": {
        "id": "doc:fda.alunbrig",
        "type": "Document",
        "documentType": "Regulatory approval",
        "name": "Alunbrig (brigatinib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Takeda Pharmaceuticals America, Inc. Alunbrig (brigatinib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/208772s013lbl.pdf. Revised February 2022. Accessed October 30, 2024.",
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            "description": "The company that manufactures the cancer drug. Only applicable to market authorization documents."
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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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            "description": "The generic name of the cancer drug, per this document. Only applicable to market authorization documents."
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            "value": null,
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            "description": "Whether this document is Active or Deprecated within moalmanac-db."
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}