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    "timestamp_received": "2026-04-06T16:31:22.257299+00:00Z",
    "timestamp_returned": "2026-04-06T16:31:22.262681+00:00Z",
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    "name": "Molecular Oncology Almanac",
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  "data": [
    {
      "id": "ind:fda.zelboraf:1",
      "indication": "ZELBORAF is indicated for the treatment of patients with Erdheim-Chester Disease with BRAF V600 mutation.",
      "initial_approval_date": "2017-11-06",
      "initial_approval_url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/202429s016lbl.pdf",
      "description": "The U.S. Food and Drug Administration granted approval to vemurafenib for the treatment of patients with Erdheim-Chester Disease and a BRAF V600 mutation.",
      "raw_biomarkers": "BRAF V600",
      "raw_cancer_type": "Erdheim-Chester Disease",
      "raw_therapeutics": "Zelboraf (vemurafenib)",
      "icd10": null,
      "regimen_code": null,
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      "document": {
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        "documentType": "Regulatory approval",
        "name": "Zelboraf (vemurafenib) [package insert]. FDA.",
        "title": null,
        "aliases": [],
        "description": "Genentech, Inc. Zelboraf (vemurafenib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/202429s019lbl.pdf. Revised May 2020. 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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            "name": "status",
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}